Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80728 |
|---|---|
| ensemblid | ENSG00000147799.12 |
| hgncid | 29351 |
| symbol | ARHGAP39 |
| name | Rho GTPase activating protein 39 |
| refseq_nuc | NM_025251.3 |
| refseq_prot | NP_079527.1 |
| ensembl_nuc | ENST00000377307.7 |
| ensembl_prot | ENSP00000366522.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 144529179 |
| end | 144685846 |
| strand | - |
| ver | v1.2 |
| region | chr8:144529179-144685846 |
| region5000 | chr8:144524179-144690846 |
| regionname0 | ARHGAP39_chr8_144529179_144685846 |
| regionname5000 | ARHGAP39_chr8_144524179_144690846 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1114 | 241 | 88 | 50 | 73 | 10 | 18 | 56 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0002 | 0/0 | 1114 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0003 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0004 | 0/0 | 1114 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0005 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3345 | 141 | 55 | 23 | 50 | 2 | 9 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0002 | 0/0 | 3345 | 71 | 21 | 17 | 21 | 5 | 7 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0003 | 0/0 | 3345 | 5 | 0 | 2 | 1 | 1 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0004 | 0/0 | 3345 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0005 | 0/0 | 3345 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0006 | 0/0 | 3345 | 4 | 0 | 2 | 0 | 2 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0007 | 0/0 | 3345 | 4 | 3 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0008 | 0/0 | 3345 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0009 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0010 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0011 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0012 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0013 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0014 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0015 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0016 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0017 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| c0018 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1486 | 183 | 45 | 44 | 67 | 9 | 17 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0002 | 0/0 | 1486 | 13 | 12 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0003 | 0/0 | 1486 | 8 | 7 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0004 | 0/0 | 1485 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0005 | 0/1 | 1486 | 6 | 0 | 4 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0006 | 0/0 | 1486 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0007 | 0/0 | 1486 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0008 | 0/0 | 1486 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0009 | 0/0 | 1486 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0010 | 0/0 | 1486 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0011 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0012 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0013 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0014 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0015 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0016 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0017 | 0/0 | 1485 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0018 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0019 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0020 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0021 | 0/0 | 1486 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0022 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| t0023 | 0/0 | 1486 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| 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 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3345 | 141 | 55 | 23 | 50 | 2 | 9 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002 | 0/0 | 3345 | 71 | 21 | 17 | 21 | 5 | 7 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0003 | 0/0 | 3345 | 5 | 0 | 2 | 1 | 1 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0004 | 0/0 | 3345 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0005 | 0/0 | 3345 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0006 | 0/0 | 3345 | 4 | 0 | 2 | 0 | 2 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0007 | 0/0 | 3345 | 4 | 3 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0010 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0012 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0014 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0015 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0016 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0017 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0018 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0002c0008 | 0/0 | 3345 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0003c0011 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0004c0009 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0005c0013 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4830 | 95 | 21 | 18 | 45 | 1 | 9 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0002 | 0/0 | 4830 | 11 | 10 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0003 | 0/0 | 4830 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0004 | 0/0 | 4829 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0005 | 0/1 | 4830 | 6 | 0 | 4 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0007 | 0/0 | 4830 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0008 | 0/0 | 4830 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0011 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0012 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0013 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0014 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0015 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0016 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0018 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0020 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0001t0021 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002t0001 | 0/0 | 4830 | 67 | 20 | 17 | 18 | 5 | 7 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002t0009 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002t0019 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002t0022 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0002t0023 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0003t0001 | 0/0 | 4830 | 4 | 0 | 2 | 0 | 1 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0003t0009 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0004t0006 | 0/0 | 4830 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0005t0001 | 0/0 | 4830 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0005t0010 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0006t0001 | 0/0 | 4830 | 4 | 0 | 2 | 0 | 2 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0007t0001 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0007t0003 | 0/0 | 4830 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0007t0017 | 0/0 | 4829 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0010t0001 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0012t0002 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0014t0007 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0015t0001 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0016t0001 | 0/0 | 4830 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0017t0001 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0001c0018t0001 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0002c0008t0001 | 0/0 | 4830 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0003c0011t0001 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0004c0009t0001 | 0/0 | 4830 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| a0005c0013t0002 | 0/0 | 4830 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | copy fasta | chr8 | 144524179 | 144690846 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0015g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0001t0021g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0022g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0002t0023g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0003t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0003t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0004t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0004t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0004t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0004t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0004t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0005t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0005t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0005t0010g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0006t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0006t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0007t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0007t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0007t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0010t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0012t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0014t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0015t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0016t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0017t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0001c0018t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0002c0008t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0002c0008t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0003c0011t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0004c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| a0005c0013t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0006 | t0001 | g0182 | EUR | GBR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0103 | EUR | GBR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0012 | EUR | FIN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | FIN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0165 | EUR | FIN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0243 | EUR | FIN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00408 | hp2 | a0004 | c0009 | t0001 | g0008 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00438 | hp1 | a0001 | c0001 | t0014 | g0054 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00558 | hp2 | a0002 | c0008 | t0001 | g0142 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0011 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG00741 | hp2 | a0001 | c0006 | t0001 | g0181 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01081 | hp1 | a0001 | c0016 | t0001 | g0091 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01081 | hp2 | a0001 | c0006 | t0001 | g0193 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0187 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01168 | hp2 | a0001 | c0010 | t0001 | g0009 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0006 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0112 | EUR | IBS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0171 | EUR | IBS | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0010 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02129 | hp1 | a0001 | c0001 | t0015 | g0180 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02155 | hp1 | a0002 | c0008 | t0001 | g0067 | EAS | CDX | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02155 | hp2 | a0001 | c0002 | t0023 | g0246 | EAS | CDX | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02257 | hp1 | a0001 | c0007 | t0003 | g0078 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0022 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02280 | hp1 | a0001 | c0007 | t0001 | g0017 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02300 | hp2 | a0001 | c0005 | t0010 | g0001 | AMR | PEL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0239 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02622 | hp1 | a0005 | c0013 | t0002 | g0195 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02630 | hp1 | a0003 | c0011 | t0001 | g0072 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02723 | hp1 | a0001 | c0012 | t0002 | g0128 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02886 | hp1 | a0001 | c0004 | t0006 | g0075 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02922 | hp2 | a0001 | c0004 | t0006 | g0073 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02965 | hp2 | a0001 | c0004 | t0006 | g0074 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02970 | hp1 | a0001 | c0004 | t0006 | g0069 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0121 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03195 | hp1 | a0001 | c0014 | t0007 | g0240 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03195 | hp2 | a0001 | c0007 | t0017 | g0019 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0062 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03486 | hp1 | a0001 | c0018 | t0001 | g0230 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03540 | hp2 | a0001 | c0002 | t0019 | g0125 | AFR | GWD | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG04204 | hp2 | a0001 | c0007 | t0003 | g0118 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0168 | AFR | YRI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | YRI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18906 | hp2 | a0001 | c0004 | t0006 | g0070 | AFR | YRI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18962 | hp1 | a0001 | c0003 | t0009 | g0004 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18967 | hp1 | a0001 | c0002 | t0009 | g0028 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18971 | hp2 | a0001 | c0015 | t0001 | g0101 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18995 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19000 | hp1 | a0001 | c0002 | t0022 | g0217 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19030 | hp1 | a0001 | c0001 | t0016 | g0105 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19082 | hp1 | a0001 | c0001 | t0012 | g0040 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19091 | hp1 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | ASW | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ASW | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02109 | hp2 | a0001 | c0001 | t0020 | g0079 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | USA | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | USA | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA21309 | hp1 | a0001 | c0017 | t0001 | g0064 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | LWK | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0186 | REF | REF | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | ARHGAP39_chr8_144524179_144690846 | ARHGAP39 | chr8 | 144524179 | 144690846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144545770
|
C | T | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2000G>A | p.Arg667Gln | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/12 | 2242/4830 | 2000/3345 | 667/1114 | chr8 | 144545770 | ||
| chr8:144547180
|
C | T | 1 | a0002 | 2 | HG00558.hp2 HG02155.hp1 |
missense_variant | MODERATE | c.1906G>A | p.Val636Ile | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 2148/4830 | 1906/3345 | 636/1114 | chr8 | 144547180 | ||
| chr8:144547677
|
T | C | 1 | a0004 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1409A>G | p.Glu470Gly | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1651/4830 | 1409/3345 | 470/1114 | chr8 | 144547677 | ||
| chr8:144547852
|
C | G | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1234G>C | p.Ala412Pro | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1476/4830 | 1234/3345 | 412/1114 | chr8 | 144547852 | ||
| chr8:144548227
|
G | C | 1 | a0003 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.859C>G | p.Pro287Ala | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1101/4830 | 859/3345 | 287/1114 | chr8 | 144548227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144530515
|
C | T | 1 | a0001c0016 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.3252G>A | p.Pro1084Pro | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 3494/4830 | 3252/3345 | 1084/1114 | chr8 | 144530515 | ||
| chr8:144530786
|
G | A | 5 | a0001c0002a0001c0003a0001c0006others(2): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
synonymous_variant | LOW | c.3066C>T | p.Asp1022Asp | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 11/12 | 3308/4830 | 3066/3345 | 1022/1114 | chr8 | 144530786 | ||
| chr8:144534186
|
C | T | 1 | a0001c0015 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.2631G>A | p.Thr877Thr | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/12 | 2873/4830 | 2631/3345 | 877/1114 | chr8 | 144534186 | ||
| chr8:144545316
|
G | A | 2 | a0001c0004a0001c0007 | 9 | HG02257.hp1 HG02280.hp1 HG02886.hp1 others(6): Show |
synonymous_variant | LOW | c.2454C>T | p.Thr818Thr | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/12 | 2696/4830 | 2454/3345 | 818/1114 | chr8 | 144545316 | ||
| chr8:144547457
|
G | A | 1 | a0001c0017 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1629C>T | p.Ala543Ala | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1871/4830 | 1629/3345 | 543/1114 | chr8 | 144547457 | ||
| chr8:144547481
|
G | A | 1 | a0001c0018 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1605C>T | p.Pro535Pro | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1847/4830 | 1605/3345 | 535/1114 | chr8 | 144547481 | ||
| chr8:144547781
|
C | G | 1 | a0001c0014 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1305G>C | p.Leu435Leu | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1547/4830 | 1305/3345 | 435/1114 | chr8 | 144547781 | ||
| chr8:144547952
|
A | G | 1 | a0001c0012 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1134T>C | p.Cys378Cys | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1376/4830 | 1134/3345 | 378/1114 | chr8 | 144547952 | ||
| chr8:144548087
|
T | C | 1 | a0001c0010 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.999A>G | p.Gln333Gln | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 1241/4830 | 999/3345 | 333/1114 | chr8 | 144548087 | ||
| chr8:144548405
|
G | C | 1 | a0001c0004 | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
synonymous_variant | LOW | c.681C>G | p.Ala227Ala | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/12 | 923/4830 | 681/3345 | 227/1114 | chr8 | 144548405 | ||
| chr8:144580878
|
C | T | 1 | a0001c0006 | 4 | HG00099.hp1 HG00741.hp2 HG01081.hp2 others(1): Show |
synonymous_variant | LOW | c.480G>A | p.Ala160Ala | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/12 | 722/4830 | 480/3345 | 160/1114 | chr8 | 144580878 | ||
| chr8:144605603
|
C | T | 5 | a0001c0003a0001c0005a0001c0010others(2): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
synonymous_variant | LOW | c.12G>A | p.Thr4Thr | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/12 | 254/4830 | 12/3345 | 4/1114 | chr8 | 144605603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144529209
|
TC | T | 2 | a0001c0001t0004a0001c0007t0017 | 9 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1212delG | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 1212 | chr8 | 144529209 | |||||
| chr8:144529234
|
G | T | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0016others(5): Show | 25 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1188C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 1188 | chr8 | 144529234 | |||||
| chr8:144529368
|
A | T | 1 | a0001c0001t0015 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 1054 | chr8 | 144529368 | |||||
| chr8:144529467
|
G | A | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(5): Show | 25 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*955C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 955 | chr8 | 144529467 | |||||
| chr8:144529476
|
C | T | 1 | a0001c0001t0008 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*946G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 946 | chr8 | 144529476 | |||||
| chr8:144529587
|
A | G | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 835 | chr8 | 144529587 | |||||
| chr8:144529593
|
C | T | 1 | a0001c0004t0006 | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*829G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 829 | chr8 | 144529593 | |||||
| chr8:144529684
|
C | T | 1 | a0001c0001t0013 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 738 | chr8 | 144529684 | |||||
| chr8:144529766
|
T | C | 1 | a0001c0001t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 656 | chr8 | 144529766 | |||||
| chr8:144529858
|
C | T | 1 | a0001c0001t0004 | 8 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*564G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 564 | chr8 | 144529858 | |||||
| chr8:144529882
|
G | A | 1 | a0001c0002t0019 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 540 | chr8 | 144529882 | |||||
| chr8:144529888
|
C | T | 1 | a0001c0001t0012 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 534 | chr8 | 144529888 | |||||
| chr8:144529981
|
T | C | 2 | a0001c0002t0009a0001c0003t0009 | 2 | NA18962.hp1 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*441A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 441 | chr8 | 144529981 | |||||
| chr8:144530013
|
G | A | 3 | a0001c0001t0002a0001c0012t0002a0005c0013t0002 | 13 | HG01975.hp2 HG02280.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*409C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 409 | chr8 | 144530013 | |||||
| chr8:144530177
|
G | A | 1 | a0001c0001t0005 | 6 | HG00323.hp2 HG00735.hp2 HG01168.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*245C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 245 | chr8 | 144530177 | |||||
| chr8:144530252
|
C | T | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0020others(4): Show | 19 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 170 | chr8 | 144530252 | |||||
| chr8:144530291
|
A | G | 1 | a0001c0001t0011 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 131 | chr8 | 144530291 | |||||
| chr8:144530300
|
G | A | 1 | a0001c0001t0005 | 6 | HG00323.hp2 HG00735.hp2 HG01168.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 122 | chr8 | 144530300 | |||||
| chr8:144530310
|
G | A | 3 | a0001c0001t0002a0001c0012t0002a0005c0013t0002 | 13 | HG01975.hp2 HG02280.hp2 HG02615.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*112C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 112 | chr8 | 144530310 | |||||
| chr8:144530311
|
G | A | 1 | a0001c0001t0020 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 111 | chr8 | 144530311 | |||||
| chr8:144530358
|
G | A | 1 | a0001c0001t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 12/12 | 64 | chr8 | 144530358 | |||||
| chr8:144605629
|
G | A | 1 | a0001c0002t0022 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/12 | 15 | chr8 | 144605629 | |||||
| chr8:144685785
|
C | T | 1 | a0001c0005t0010 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-181G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/12 | 80171 | chr8 | 144685785 | |||||
| chr8:144685829
|
G | A | 1 | a0001c0002t0023 | 1 | HG02155.hp2 | 5_prime_UTR_variant | MODIFIER | c.-225C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/12 | 80215 | chr8 | 144685829 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:144530621
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | splice_region_variant&intron_variant | LOW | c.3151-5A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 11/11 | chr8 | 144530621 | ||||||
| chr8:144530636
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3151-20C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 11/11 | chr8 | 144530636 | ||||||
| chr8:144530947
|
T | C | 221 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2981-76A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144530947 | ||||||
| chr8:144530986
|
G | A | 154 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2981-115C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144530986 | ||||||
| chr8:144531045
|
G | A | 41 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0223others(38): Show | 41 | HG01975.hp2 HG02145.hp2 HG02257.hp2 others(38): Show |
intron_variant | MODIFIER | c.2981-174C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531045 | ||||||
| chr8:144531052
|
G | A | 136 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(133): Show | 136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2981-181C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531052 | ||||||
| chr8:144531053
|
G | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(14): Show | 17 | HG02004.hp1 HG02135.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.2981-182C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531053 | ||||||
| chr8:144531064
|
T | C | 7 | a0001c0001t0001g0238a0001c0001t0003g0023a0001c0001t0008g0120others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2981-193A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531064 | ||||||
| chr8:144531065
|
C | G | 11 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2981-194G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531065 | ||||||
| chr8:144531065
|
C | T | 159 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(156): Show | 159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2981-194G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531065 | ||||||
| chr8:144531081
|
T | A | 27 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0001t0002g0131others(24): Show | 27 | HG01192.hp2 HG01975.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2981-210A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531081 | ||||||
| chr8:144531127
|
T | G | 31 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0001t0002g0131others(28): Show | 31 | HG01891.hp1 HG01975.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2981-256A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531127 | ||||||
| chr8:144531128
|
C | A | 31 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0001t0002g0131others(28): Show | 31 | HG01891.hp1 HG01975.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2981-257G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531128 | ||||||
| chr8:144531144
|
G | A | 1 | a0001c0002t0022g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2981-273C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531144 | ||||||
| chr8:144531174
|
T | TGAAGGGC others(163): Show |
1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2981-304_2981-303i others(172): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531174 | ||||||
| chr8:144531174
|
T | TGAAGGGC others(156): Show |
3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2981-304_2981-303i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531174 | ||||||
| chr8:144531174
|
T | TGAAGGGC others(725): Show |
1 | a0001c0002t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2981-304_2981-303i others(734): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531174 | ||||||
| chr8:144531183
|
C | CAGGGCAG others(45): Show |
5 | a0001c0001t0002g0123a0001c0001t0002g0131a0001c0001t0002g0134others(2): Show | 5 | HG01975.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2981-313_2981-312i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531183 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(45): Show |
1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(156): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(229): Show |
1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(238): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(805): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0151 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(814): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1148): Show |
1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1157): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1436): Show |
1 | a0001c0002t0001g0051 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1445): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1096): Show |
1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1105): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(992): Show |
1 | a0001c0002t0001g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1001): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1311): Show |
1 | a0001c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1320): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1103): Show |
1 | a0001c0002t0001g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1112): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(964): Show |
1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(973): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(156): Show |
1 | a0001c0002t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(274): Show |
1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(283): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(52): Show |
12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0036others(9): Show | 12 | HG00438.hp1 HG02004.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.2981-379_2981-321d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(555): Show |
1 | a0001c0002t0001g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(564): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(940): Show |
1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(949): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(888): Show |
1 | a0001c0002t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(897): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(288): Show |
1 | a0001c0001t0001g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(297): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(503): Show |
1 | a0001c0002t0001g0114 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(512): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(503): Show |
1 | a0001c0002t0001g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(512): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(822): Show |
1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(831): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1041): Show |
1 | a0001c0002t0001g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1050): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(555): Show |
1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(564): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(829): Show |
1 | a0001c0015t0001g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(838): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(666): Show |
2 | a0001c0002t0001g0094a0001c0002t0001g0113 | 2 | HG00609.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(675): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(933): Show |
3 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0089 | 3 | HG02683.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(942): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(2824): Show |
1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(2833): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(777): Show |
1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(786): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(881): Show |
2 | a0001c0002t0001g0013a0001c0002t0001g0164 | 2 | HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(890): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(718): Show |
6 | a0001c0002t0001g0003a0001c0002t0001g0088a0001c0002t0001g0106others(3): Show | 6 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2981-321_2981-320i others(727): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(555): Show |
3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0099 | 3 | HG00280.hp2 HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(564): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(496): Show |
1 | a0001c0002t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(505): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(843): Show |
1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(852): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(1131): Show |
1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(1140): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(45): Show |
3 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0191 | 3 | HG03491.hp2 HG03688.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(444): Show |
1 | a0001c0002t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(453): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(156): Show |
1 | a0001c0001t0001g0100 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(510): Show |
1 | a0001c0001t0001g0209 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2981-321_2981-320i others(519): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(829): Show |
2 | a0001c0002t0001g0093a0001c0002t0001g0216 | 2 | HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2981-321_2981-320i others(838): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(666): Show |
1 | a0001c0002t0001g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(675): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | AGAGCAGC others(777): Show |
1 | a0001c0002t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2981-321_2981-320i others(786): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | C | 9 | a0001c0001t0001g0184a0001c0001t0002g0123a0001c0001t0002g0131others(6): Show | 9 | HG01975.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2981-320T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
A | G | 14 | a0001c0001t0001g0122a0001c0001t0002g0139a0001c0001t0002g0145others(11): Show | 14 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2981-320T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
AGAGCAGC others(52): Show |
A | 1 | a0001c0002t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2981-379_2981-321d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
AGAGCAGC others(170): Show |
A | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2981-497_2981-321d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
AGAGCAGC others(229): Show |
A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2981-556_2981-321d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531191
|
AGAGCAGC others(878): Show |
A | 7 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2980+229_2981-321d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531191 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(97): Show |
1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2981-322_2981-321i others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(97): Show |
4 | a0001c0002t0001g0015a0001c0002t0001g0025a0001c0002t0001g0140others(1): Show | 4 | HG03139.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2981-322_2981-321i others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(853): Show |
2 | a0001c0003t0009g0004a0004c0009t0001g0008 | 2 | HG00408.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2981-322_2981-321i others(862): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(801): Show |
1 | a0001c0003t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2981-322_2981-321i others(810): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(586): Show |
1 | a0001c0003t0001g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2981-322_2981-321i others(595): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(801): Show |
1 | a0001c0002t0009g0028 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2981-322_2981-321i others(810): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(149): Show |
1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2981-322_2981-321i others(158): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(104): Show |
1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2981-322_2981-321i others(113): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531192
|
G | GAGCAGCA others(97): Show |
1 | a0001c0002t0019g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2981-322_2981-321i others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531192 | ||||||
| chr8:144531206
|
G | A | 21 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(18): Show | 21 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.2981-335C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531206 | ||||||
| chr8:144531207
|
A | T | 34 | a0001c0001t0001g0122a0001c0001t0001g0223a0001c0001t0001g0224others(31): Show | 34 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2981-336T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531207 | ||||||
| chr8:144531208
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2981-337C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531208 | ||||||
| chr8:144531210
|
G | A | 11 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166others(8): Show | 11 | HG00323.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2981-339C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531210 | ||||||
| chr8:144531210
|
G | AGGCTAGA others(104): Show |
1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2981-339_2981-338i others(113): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531210 | ||||||
| chr8:144531212
|
G | A | 34 | a0001c0001t0001g0122a0001c0001t0001g0223a0001c0001t0001g0224others(31): Show | 34 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2981-341C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531212 | ||||||
| chr8:144531215
|
A | G | 34 | a0001c0001t0001g0122a0001c0001t0001g0223a0001c0001t0001g0224others(31): Show | 34 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.2981-344T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531215 | ||||||
| chr8:144531220
|
T | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0223others(32): Show | 35 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.2981-349A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531220 | ||||||
| chr8:144531225
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0007g0018a0001c0001t0007g0168others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2981-354C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531225 | ||||||
| chr8:144531230
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0207a0005c0013t0002g0195 | 3 | HG02080.hp2 HG02622.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2981-359C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531230 | ||||||
| chr8:144531233
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0207 | 2 | HG02080.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2981-362T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531233 | ||||||
| chr8:144531235
|
AAGGGCAC | A | 78 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0050others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2981-371_2981-365d others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531235
|
AAGGGCAC others(59): Show |
A | 3 | a0001c0001t0001g0211a0001c0001t0004g0153a0001c0001t0007g0239 | 3 | HG02055.hp1 HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2981-430_2981-365d others(68): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531235
|
AAGGGCAC others(118): Show |
A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0007g0168 | 3 | HG02486.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2981-489_2981-365d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531235
|
AAGGGCAC others(472): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2980+591_2981-365d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531235
|
AAGGGCAC others(531): Show |
A | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2980+532_2981-365d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531235
|
AAGGGCAC others(590): Show |
A | 4 | a0001c0001t0004g0152a0001c0001t0004g0154a0001c0001t0004g0156others(1): Show | 4 | HG02976.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2980+473_2981-365d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531235 | ||||||
| chr8:144531237
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2981-366C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531237 | ||||||
| chr8:144531241
|
A | AGCGAGCA others(35): Show |
1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2981-371_2981-370i others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531241 | ||||||
| chr8:144531241
|
A | AGCGAGCA others(38): Show |
1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2981-371_2981-370i others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531241 | ||||||
| chr8:144531241
|
A | AGCGAGCA others(156): Show |
4 | a0001c0001t0001g0122a0001c0001t0002g0139a0001c0001t0002g0170others(1): Show | 4 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2981-371_2981-370i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531241 | ||||||
| chr8:144531241
|
A | AGCGAGCA others(97): Show |
1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2981-371_2981-370i others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531241 | ||||||
| chr8:144531241
|
A | AGCGAGCA others(156): Show |
2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2981-371_2981-370i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531241 | ||||||
| chr8:144531242
|
C | A | 8 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0229others(5): Show | 8 | HG01981.hp2 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2981-371G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531242
|
C | CAGGGCAG others(97): Show |
1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2981-372_2981-371i others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531242
|
C | CAGGGCAG others(503): Show |
1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2981-372_2981-371i others(512): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531242
|
C | CAGGGCAG others(45): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0196a0001c0001t0001g0213 | 3 | HG01071.hp1 HG01358.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2981-423_2981-372d others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531242
|
C | CAGGGCAG others(333): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2981-372_2981-371i others(342): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531242
|
C | CAGGGCAG others(45): Show |
1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2981-372_2981-371i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531242 | ||||||
| chr8:144531244
|
G | A | 5 | a0001c0005t0001g0006a0001c0005t0001g0010a0001c0005t0001g0011others(2): Show | 5 | HG00639.hp1 HG01168.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2981-373C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531244 | ||||||
| chr8:144531244
|
G | GGGCAGGG others(45): Show |
1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2981-374_2981-373i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531244 | ||||||
| chr8:144531250
|
C | A | 3 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0007t0003g0078 | 3 | HG02080.hp2 HG02257.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2981-379G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531250 | ||||||
| chr8:144531250
|
C | G | 27 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0058others(24): Show | 27 | HG00323.hp1 HG00609.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.2981-379G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531250 | ||||||
| chr8:144531250
|
CGAGCAGC others(524): Show |
C | 3 | a0001c0001t0003g0023a0001c0001t0021g0062a0001c0014t0007g0240 | 3 | HG03195.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+524_2981-380d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531250 | ||||||
| chr8:144531253
|
G | GCAGCAGG others(45): Show |
1 | a0001c0005t0001g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2981-383_2981-382i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531253 | ||||||
| chr8:144531253
|
G | GCAGCAGG others(340): Show |
1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2981-383_2981-382i others(349): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531253 | ||||||
| chr8:144531265
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2981-394C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531265 | ||||||
| chr8:144531266
|
A | T | 10 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0082others(7): Show | 10 | HG02132.hp2 HG02257.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2981-395T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531266 | ||||||
| chr8:144531269
|
G | A | 9 | a0001c0001t0001g0039a0001c0002t0001g0020a0001c0002t0001g0165others(6): Show | 9 | HG00323.hp1 HG01192.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2981-398C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531269 | ||||||
| chr8:144531269
|
G | GGACTGGA others(96): Show |
1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2981-399_2981-398i others(105): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531269 | ||||||
| chr8:144531269
|
GGGCTAGA others(52): Show |
G | 4 | a0001c0001t0001g0042a0001c0001t0001g0141a0001c0001t0001g0179others(1): Show | 4 | HG00609.hp2 HG06807.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.2981-457_2981-399d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531269 | ||||||
| chr8:144531269
|
GGGCTAGA others(406): Show |
G | 1 | a0001c0001t0001g0220 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2980+623_2981-399d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531269 | ||||||
| chr8:144531269
|
GGGCTAGA others(760): Show |
G | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2980+269_2981-399d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531269 | ||||||
| chr8:144531271
|
G | A | 9 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0082others(6): Show | 9 | HG02132.hp2 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2981-400C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531271 | ||||||
| chr8:144531274
|
A | G | 9 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0082others(6): Show | 9 | HG02132.hp2 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2981-403T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531274 | ||||||
| chr8:144531279
|
T | C | 9 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0082others(6): Show | 9 | HG02132.hp2 HG02257.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2981-408A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531279 | ||||||
| chr8:144531284
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2981-413C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531284 | ||||||
| chr8:144531288
|
C | CAGCAGAA others(392): Show |
1 | a0001c0002t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2981-418_2981-417i others(401): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531288 | ||||||
| chr8:144531289
|
G | A | 4 | a0001c0001t0001g0190a0001c0001t0001g0228a0001c0001t0002g0131others(1): Show | 4 | HG02080.hp2 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2981-418C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531289 | ||||||
| chr8:144531292
|
A | T | 3 | a0001c0001t0001g0190a0001c0001t0002g0131a0001c0001t0002g0134 | 3 | HG02080.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2981-421T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531292 | ||||||
| chr8:144531294
|
AAGGGCAC | A | 10 | a0001c0001t0001g0143a0001c0002t0001g0082a0001c0002t0001g0083others(7): Show | 10 | HG01168.hp2 HG01192.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2981-430_2981-424d others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(59): Show |
A | 3 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0002t0001g0133 | 3 | HG02027.hp2 NA19012.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2981-489_2981-424d others(68): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(118): Show |
A | 2 | a0001c0002t0001g0038a0001c0002t0001g0041 | 2 | HG02132.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2981-548_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(177): Show |
A | 1 | a0001c0001t0001g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2981-607_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(295): Show |
A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2980+709_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(354): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2980+650_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(413): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2980+591_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531294
|
AAGGGCAC others(472): Show |
A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2980+532_2981-424d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531294 | ||||||
| chr8:144531301
|
C | CAGGGCAG others(45): Show |
2 | a0001c0001t0002g0131a0001c0001t0002g0134 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2981-431_2981-430i others(54): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531301 | ||||||
| chr8:144531303
|
G | A | 1 | a0001c0002t0022g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2981-432C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531303 | ||||||
| chr8:144531309
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2981-438C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531309 | ||||||
| chr8:144531309
|
G | C | 51 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0039others(48): Show | 51 | HG01074.hp2 HG01168.hp2 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.2981-438C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531309 | ||||||
| chr8:144531309
|
G | GGAGCAGC others(333): Show |
1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2981-439_2981-438i others(342): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531309 | ||||||
| chr8:144531309
|
G | GGAGCAGC others(104): Show |
1 | a0001c0001t0005g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2981-439_2981-438i others(113): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531309 | ||||||
| chr8:144531312
|
G | A | 4 | a0001c0005t0001g0006a0001c0005t0001g0010a0001c0005t0010g0001others(1): Show | 4 | HG01168.hp2 HG01192.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2981-441C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531312 | ||||||
| chr8:144531325
|
A | T | 6 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG00323.hp1 HG01192.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2981-454T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531325 | ||||||
| chr8:144531328
|
A | G | 170 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2981-457T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531328 | ||||||
| chr8:144531330
|
G | A | 5 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(2): Show | 5 | HG00323.hp1 HG01192.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2981-459C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531330 | ||||||
| chr8:144531333
|
A | G | 5 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(2): Show | 5 | HG00323.hp1 HG01192.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2981-462T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531333 | ||||||
| chr8:144531338
|
T | C | 5 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(2): Show | 5 | HG00323.hp1 HG01192.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2981-467A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531338 | ||||||
| chr8:144531338
|
T | TAGCAGGC others(267): Show |
1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2981-468_2981-467i others(276): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531338 | ||||||
| chr8:144531343
|
G | A | 3 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG02615.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2981-472C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531343 | ||||||
| chr8:144531348
|
G | A | 4 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(1): Show | 4 | HG01346.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2981-477C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531348 | ||||||
| chr8:144531353
|
AAGGGCAC | A | 6 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235others(3): Show | 6 | HG00323.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2981-489_2981-483d others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531353 | ||||||
| chr8:144531353
|
AAGGGCAC others(118): Show |
A | 1 | a0001c0001t0001g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2981-607_2981-483d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531353 | ||||||
| chr8:144531353
|
AAGGGCAC others(649): Show |
A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980+296_2981-483d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531353 | ||||||
| chr8:144531355
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2981-484C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531355 | ||||||
| chr8:144531359
|
A | AGCGAGCA others(35): Show |
1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2981-489_2981-488i others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531359 | ||||||
| chr8:144531362
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0124 | 3 | HG01346.hp2 HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2981-491C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531362 | ||||||
| chr8:144531368
|
C | CGAGCAGC others(111): Show |
1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2981-498_2981-497i others(120): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531368 | ||||||
| chr8:144531368
|
C | CGAGCAGC others(170): Show |
1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2981-674_2981-498d others(179): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531368 | ||||||
| chr8:144531368
|
C | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0097others(28): Show | 31 | HG01074.hp2 HG01168.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.2981-497G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531368 | ||||||
| chr8:144531387
|
G | A | 18 | a0001c0001t0001g0044a0001c0001t0001g0223a0001c0001t0001g0224others(15): Show | 18 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.2981-516C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531387 | ||||||
| chr8:144531387
|
G | GGGCTAGA others(52): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2981-517_2981-516i others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531387 | ||||||
| chr8:144531387
|
GGGCTAGA others(583): Show |
G | 3 | a0001c0001t0004g0150a0001c0001t0004g0155a0001c0001t0004g0158 | 3 | HG02055.hp2 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980+328_2981-517d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531387 | ||||||
| chr8:144531412
|
AAGGGCAC | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2981-548_2981-542d others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531412 | ||||||
| chr8:144531414
|
G | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG00558.hp1 NA18997.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2981-543C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531414 | ||||||
| chr8:144531421
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0041 | 2 | HG02132.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2981-550C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531421 | ||||||
| chr8:144531427
|
G | C | 93 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0097others(90): Show | 93 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2981-556C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531427 | ||||||
| chr8:144531427
|
G | GGAGCAGC others(52): Show |
2 | a0001c0001t0001g0045a0001c0002t0019g0125 | 2 | HG03540.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2981-615_2981-557d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531427 | ||||||
| chr8:144531427
|
G | GGAGCAGC others(111): Show |
6 | a0001c0001t0001g0100a0001c0002t0001g0025a0001c0002t0001g0140others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2981-557_2981-556i others(120): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531427 | ||||||
| chr8:144531427
|
G | GGAGCAGC others(163): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0210a0001c0001t0015g0180 | 3 | HG02129.hp1 NA18969.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2981-557_2981-556i others(172): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531427 | ||||||
| chr8:144531427
|
GGAGCAGC others(52): Show |
G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0005g0243 | 3 | HG00323.hp2 HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2981-615_2981-557d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531427 | ||||||
| chr8:144531443
|
A | T | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2981-572T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531443 | ||||||
| chr8:144531446
|
G | A | 10 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(7): Show | 10 | HG00099.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2981-575C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531446 | ||||||
| chr8:144531446
|
G | GGGCTAGA others(52): Show |
1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2981-576_2981-575i others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531446 | ||||||
| chr8:144531448
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2981-577C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531448 | ||||||
| chr8:144531451
|
A | G | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2981-580T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531451 | ||||||
| chr8:144531456
|
T | C | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2981-585A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531456 | ||||||
| chr8:144531466
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-595C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531466 | ||||||
| chr8:144531469
|
A | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-598T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531469 | ||||||
| chr8:144531471
|
AAGGGCAC | A | 3 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0126 | 3 | HG02132.hp2 HG03225.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2981-607_2981-601d others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531471 | ||||||
| chr8:144531486
|
C | G | 35 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0097others(32): Show | 35 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.2981-615G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531486 | ||||||
| chr8:144531486
|
C | GGAGCAGC others(288): Show |
1 | a0001c0001t0001g0061 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2981-615_2981-614i others(297): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531486 | ||||||
| chr8:144531486
|
CGAGCAGC others(52): Show |
C | 1 | a0001c0001t0007g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2981-674_2981-616d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531486 | ||||||
| chr8:144531487
|
G | A | 2 | a0001c0002t0001g0038a0001c0002t0001g0041 | 2 | HG02132.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2981-616C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531487 | ||||||
| chr8:144531502
|
A | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-631T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531502 | ||||||
| chr8:144531505
|
G | A | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG02258.hp2 HG02280.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.2981-634C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531505 | ||||||
| chr8:144531505
|
GGGCTAGA others(524): Show |
G | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2980+269_2981-635d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531505 | ||||||
| chr8:144531507
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-636C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531507 | ||||||
| chr8:144531510
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-639T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531510 | ||||||
| chr8:144531515
|
T | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-644A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531515 | ||||||
| chr8:144531520
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2981-649C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531520 | ||||||
| chr8:144531525
|
G | A | 2 | a0001c0002t0001g0124a0005c0013t0002g0195 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2981-654C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531525 | ||||||
| chr8:144531530
|
AAGGGCAC others(413): Show |
A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2980+355_2981-660d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531530 | ||||||
| chr8:144531539
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2981-668C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531539 | ||||||
| chr8:144531543
|
A | AACACTAG others(37): Show |
1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2981-673_2981-672i others(46): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531543 | ||||||
| chr8:144531544
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2981-673C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531544 | ||||||
| chr8:144531545
|
G | C | 73 | a0001c0001t0001g0044a0001c0001t0001g0100a0001c0001t0002g0131others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.2981-674C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531545 | ||||||
| chr8:144531545
|
G | GGAGCAGC others(229): Show |
1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2981-675_2981-674i others(238): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531545 | ||||||
| chr8:144531545
|
G | GGAGCAGC others(229): Show |
1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2981-675_2981-674i others(238): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531545 | ||||||
| chr8:144531546
|
G | C | 1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2981-675C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531546 | ||||||
| chr8:144531564
|
G | A | 16 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(13): Show | 16 | HG01192.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2981-693C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531564 | ||||||
| chr8:144531564
|
GGGCTAGA others(111): Show |
G | 2 | a0001c0001t0001g0173a0001c0001t0001g0205 | 2 | HG02027.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2980+623_2981-694d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531564 | ||||||
| chr8:144531564
|
GGGCTAGA others(406): Show |
G | 1 | a0001c0002t0001g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2980+328_2981-694d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531564 | ||||||
| chr8:144531575
|
A | AATCCGGG others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2981-705_2981-704i others(12): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531575 | ||||||
| chr8:144531576
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2981-705C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531576 | ||||||
| chr8:144531604
|
G | C | 16 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0149others(13): Show | 16 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2980+701C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531604 | ||||||
| chr8:144531604
|
GGAGCAGC others(229): Show |
G | 1 | a0001c0001t0004g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2980+465_2980+700d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531604 | ||||||
| chr8:144531623
|
G | A | 22 | a0001c0001t0001g0122a0001c0001t0001g0223a0001c0001t0001g0224others(19): Show | 22 | HG01975.hp1 HG01975.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2980+682C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531623 | ||||||
| chr8:144531623
|
GGGCTAGA others(52): Show |
G | 1 | a0001c0001t0001g0042 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2980+623_2980+681d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531623 | ||||||
| chr8:144531623
|
GGGCTAGA others(347): Show |
G | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2980+328_2980+681d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531623 | ||||||
| chr8:144531633
|
T | TAGCAGGC others(333): Show |
3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2980+671_2980+672i others(342): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531633 | ||||||
| chr8:144531633
|
T | TAGCAGGC others(156): Show |
2 | a0001c0001t0001g0024a0001c0017t0001g0064 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2980+671_2980+672i others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531633 | ||||||
| chr8:144531654
|
ACAGGGCA others(56): Show |
A | 1 | a0001c0002t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2980+588_2980+650d others(65): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531654 | ||||||
| chr8:144531654
|
ACAGGGCA others(115): Show |
A | 1 | a0001c0002t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2980+529_2980+650d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531654 | ||||||
| chr8:144531663
|
G | C | 14 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG02132.hp1 HG02258.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2980+642C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531663 | ||||||
| chr8:144531676
|
G | GGGAGTGG others(52): Show |
4 | a0001c0001t0001g0065a0001c0001t0001g0190a0001c0001t0001g0210others(1): Show | 4 | HG02080.hp2 HG02129.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2980+628_2980+629i others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531676 | ||||||
| chr8:144531679
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+626T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531679 | ||||||
| chr8:144531681
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2980+624A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531681 | ||||||
| chr8:144531682
|
A | AGGCTAGA others(406): Show |
1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2980+622_2980+623i others(415): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531682 | ||||||
| chr8:144531682
|
A | G | 112 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2980+623T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531682 | ||||||
| chr8:144531682
|
AGGCTAGA others(170): Show |
A | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0208others(2): Show | 5 | HG00323.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980+446_2980+622d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531682 | ||||||
| chr8:144531684
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+621C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531684 | ||||||
| chr8:144531687
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+618T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531687 | ||||||
| chr8:144531692
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+613A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531692 | ||||||
| chr8:144531702
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2980+603C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531702 | ||||||
| chr8:144531709
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+596C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531709 | ||||||
| chr8:144531722
|
G | C | 28 | a0001c0001t0001g0024a0001c0001t0001g0136a0001c0001t0001g0146others(25): Show | 28 | HG01074.hp2 HG01099.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.2980+583C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531722 | ||||||
| chr8:144531741
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0228others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980+564C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531741 | ||||||
| chr8:144531741
|
GGGCTAGA others(288): Show |
G | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2980+269_2980+563d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531741 | ||||||
| chr8:144531781
|
G | C | 45 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0047others(42): Show | 45 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.2980+524C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531781 | ||||||
| chr8:144531781
|
GGAGCAGC others(52): Show |
G | 8 | a0001c0001t0001g0136a0001c0001t0001g0146a0001c0001t0001g0179others(5): Show | 8 | HG01192.hp2 HG01346.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2980+465_2980+523d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531781 | ||||||
| chr8:144531800
|
G | A | 12 | a0001c0001t0001g0194a0001c0001t0001g0202a0001c0001t0001g0225others(9): Show | 12 | HG01074.hp2 HG01099.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2980+505C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531800 | ||||||
| chr8:144531820
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01346.hp2 HG01361.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2980+485C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531820 | ||||||
| chr8:144531827
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+478C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531827 | ||||||
| chr8:144531831
|
A | AGCGAGCA others(38): Show |
1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+473_2980+474i others(47): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531831 | ||||||
| chr8:144531832
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+473G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531832 | ||||||
| chr8:144531840
|
C | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+465G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
C | CGAGCAGC others(51): Show |
1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2980+464_2980+465i others(60): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
C | CGAGCAGC others(52): Show |
53 | a0001c0001t0001g0100a0001c0001t0002g0145a0001c0002t0001g0003others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.2980+406_2980+464d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
C | CGAGCAGC others(111): Show |
1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2980+464_2980+465i others(120): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
C | CGAGCAGC others(229): Show |
1 | a0001c0002t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2980+464_2980+465i others(238): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
C | G | 38 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0061others(35): Show | 38 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2980+465G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531840
|
CGAGCAGC others(52): Show |
C | 2 | a0001c0001t0001g0194a0001c0001t0001g0202 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.2980+406_2980+464d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531840 | ||||||
| chr8:144531841
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+464C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531841 | ||||||
| chr8:144531855
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+450C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531855 | ||||||
| chr8:144531856
|
A | T | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+449T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531856 | ||||||
| chr8:144531859
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0061others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2980+446C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531859 | ||||||
| chr8:144531859
|
G | GGGCTAGA others(111): Show |
1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2980+445_2980+446i others(120): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531859 | ||||||
| chr8:144531859
|
G | GGGCTAGA others(52): Show |
46 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(43): Show | 46 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2980+445_2980+446i others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531859 | ||||||
| chr8:144531859
|
G | GGGCTAGA others(642): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.2980+445_2980+446i others(651): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531859 | ||||||
| chr8:144531859
|
GGGCTAGA others(170): Show |
G | 1 | a0001c0001t0007g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2980+269_2980+445d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531859 | ||||||
| chr8:144531861
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+444C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531861 | ||||||
| chr8:144531864
|
A | G | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+441T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531864 | ||||||
| chr8:144531869
|
T | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+436A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531869 | ||||||
| chr8:144531899
|
G | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0204a0001c0001t0001g0205others(22): Show | 25 | HG02027.hp2 HG02132.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.2980+406C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531899 | ||||||
| chr8:144531911
|
G | GGGGAGTG others(50): Show |
1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2980+393_2980+394i others(59): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531911 | ||||||
| chr8:144531916
|
G | GTAGGCTA others(52): Show |
1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2980+388_2980+389i others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531916 | ||||||
| chr8:144531918
|
G | A | 14 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0229others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2980+387C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531918 | ||||||
| chr8:144531918
|
GGGCTAGA others(52): Show |
G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0228others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2980+328_2980+386d others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531918 | ||||||
| chr8:144531938
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+367C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531938 | ||||||
| chr8:144531941
|
A | T | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+364T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531941 | ||||||
| chr8:144531944
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2980+361T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531944 | ||||||
| chr8:144531958
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+347C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531958 | ||||||
| chr8:144531958
|
G | C | 12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(9): Show | 12 | HG02258.hp2 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2980+347C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531958 | ||||||
| chr8:144531977
|
A | G | 33 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0036others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980+328T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531977 | ||||||
| chr8:144531987
|
T | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2980+318A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144531987 | ||||||
| chr8:144532017
|
G | C | 18 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(15): Show | 18 | HG02257.hp1 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2980+288C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532017 | ||||||
| chr8:144532017
|
G | GGAGCAGC others(524): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2980+287_2980+288i others(533): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532017 | ||||||
| chr8:144532018
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2980+287C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532018 | ||||||
| chr8:144532036
|
A | G | 14 | a0001c0001t0001g0024a0001c0001t0008g0120a0001c0001t0008g0121others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2980+269T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532036 | ||||||
| chr8:144532076
|
G | C | 12 | a0001c0001t0001g0024a0001c0001t0008g0120a0001c0001t0008g0121others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2980+229C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532076 | ||||||
| chr8:144532242
|
G | A | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2980+63C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | 144532242 | ||||||
| chr8:144532408
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2889-12T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532408 | ||||||
| chr8:144532456
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2889-60C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532456 | ||||||
| chr8:144532459
|
T | G | 1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2889-63A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532459 | ||||||
| chr8:144532529
|
C | T | 3 | a0001c0001t0003g0063a0001c0001t0003g0071a0001c0001t0003g0076 | 3 | HG02895.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2889-133G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532529 | ||||||
| chr8:144532545
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2889-149G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532545 | ||||||
| chr8:144532639
|
C | T | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2889-243G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532639 | ||||||
| chr8:144532676
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2889-280C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532676 | ||||||
| chr8:144532790
|
G | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2888+336C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532790 | ||||||
| chr8:144532825
|
C | A | 46 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(43): Show | 46 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2888+301G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532825 | ||||||
| chr8:144532947
|
T | C | 27 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2888+179A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144532947 | ||||||
| chr8:144533018
|
C | T | 1 | a0001c0001t0008g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2888+108G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144533018 | ||||||
| chr8:144533019
|
G | A | 4 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2888+107C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144533019 | ||||||
| chr8:144533083
|
T | C | 47 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(44): Show | 47 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2888+43A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144533083 | ||||||
| chr8:144533105
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2888+21G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144533105 | ||||||
| chr8:144533119
|
G | A | 3 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239 | 3 | HG02451.hp2 HG02572.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.2888+7C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 9/11 | chr8 | 144533119 | ||||||
| chr8:144533380
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2689-55C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533380 | ||||||
| chr8:144533394
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0151 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2689-69G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533394 | ||||||
| chr8:144533404
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2689-79G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533404 | ||||||
| chr8:144533796
|
G | A | 4 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2688+333C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533796 | ||||||
| chr8:144533814
|
T | C | 47 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(44): Show | 47 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2688+315A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533814 | ||||||
| chr8:144533863
|
G | A | 41 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0047others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2688+266C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533863 | ||||||
| chr8:144533876
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2688+253C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533876 | ||||||
| chr8:144533989
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0211 | 2 | HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2688+140C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144533989 | ||||||
| chr8:144534004
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2688+125C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144534004 | ||||||
| chr8:144534093
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2688+36G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 8/11 | chr8 | 144534093 | ||||||
| chr8:144534214
|
A | T | 44 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(41): Show | 44 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2615-12T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534214 | ||||||
| chr8:144534232
|
A | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0238a0001c0001t0003g0023others(15): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2615-30T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534232 | ||||||
| chr8:144534342
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2615-140C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534342 | ||||||
| chr8:144534419
|
C | G | 6 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2615-217G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534419 | ||||||
| chr8:144534704
|
C | T | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2615-502G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534704 | ||||||
| chr8:144534861
|
T | G | 38 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(35): Show | 38 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2615-659A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534861 | ||||||
| chr8:144534901
|
CAG | C | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2615-701_2615-700d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144534901 | ||||||
| chr8:144535046
|
G | C | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2615-844C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535046 | ||||||
| chr8:144535123
|
G | A | 4 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615-921C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535123 | ||||||
| chr8:144535263
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2615-1061A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535263 | ||||||
| chr8:144535373
|
T | TG | 3 | a0001c0001t0001g0132a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01981.hp2 NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2615-1172dupC | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535373 | ||||||
| chr8:144535384
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2615-1182C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535384 | ||||||
| chr8:144535418
|
T | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2615-1216A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535418 | ||||||
| chr8:144535425
|
A | G | 1 | a0001c0002t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2615-1223T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535425 | ||||||
| chr8:144535436
|
A | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2615-1234T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535436 | ||||||
| chr8:144535449
|
G | C | 1 | a0001c0001t0012g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2615-1247C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535449 | ||||||
| chr8:144535591
|
G | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2615-1389C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535591 | ||||||
| chr8:144535661
|
C | T | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2615-1459G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535661 | ||||||
| chr8:144535795
|
TGAA | T | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2615-1596_2615-159 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535795 | ||||||
| chr8:144535804
|
T | C | 49 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0151others(46): Show | 49 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(46): Show |
intron_variant | MODIFIER | c.2615-1602A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535804 | ||||||
| chr8:144535814
|
GTCTC | G | 4 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2615-1616_2615-161 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535814 | ||||||
| chr8:144535872
|
G | C | 22 | a0001c0001t0003g0023a0001c0001t0004g0150a0001c0001t0004g0152others(19): Show | 22 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2615-1670C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144535872 | ||||||
| chr8:144536000
|
G | C | 33 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(30): Show | 33 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.2614+1721C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536000 | ||||||
| chr8:144536130
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2614+1591G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536130 | ||||||
| chr8:144536192
|
C | T | 8 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2614+1529G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536192 | ||||||
| chr8:144536429
|
C | G | 10 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2614+1292G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536429 | ||||||
| chr8:144536446
|
T | C | 47 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(44): Show | 47 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2614+1275A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536446 | ||||||
| chr8:144536468
|
G | C | 6 | a0001c0002t0009g0028a0001c0003t0001g0005a0001c0003t0001g0012others(3): Show | 6 | HG00280.hp1 HG00408.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2614+1253C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144536468 | ||||||
| chr8:144537120
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2614+601C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537120 | ||||||
| chr8:144537210
|
G | A | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2614+511C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537210 | ||||||
| chr8:144537263
|
G | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2614+458C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537263 | ||||||
| chr8:144537429
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2614+292G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537429 | ||||||
| chr8:144537472
|
T | C | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2614+249A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537472 | ||||||
| chr8:144537628
|
A | C | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2614+93T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537628 | ||||||
| chr8:144537633
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2614+88G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537633 | ||||||
| chr8:144537706
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2614+15C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537706 | ||||||
| chr8:144537709
|
G | A | 2 | a0001c0001t0001g0122a0001c0002t0001g0159 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2614+12C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | 144537709 | ||||||
| chr8:144537884
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0197 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2522-71T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144537884 | ||||||
| chr8:144538045
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2522-232C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538045 | ||||||
| chr8:144538067
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0190a0001c0001t0001g0210others(1): Show | 4 | HG02080.hp2 HG02129.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2522-254G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538067 | ||||||
| chr8:144538189
|
T | C | 1 | a0001c0003t0009g0004 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2522-376A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538189 | ||||||
| chr8:144538292
|
C | T | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2522-479G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538292 | ||||||
| chr8:144538322
|
G | C | 4 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2522-509C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538322 | ||||||
| chr8:144538484
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2522-671G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538484 | ||||||
| chr8:144538649
|
C | T | 3 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG02615.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2522-836G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538649 | ||||||
| chr8:144538661
|
C | A | 1 | a0001c0002t0001g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2522-848G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538661 | ||||||
| chr8:144538682
|
C | T | 1 | a0001c0007t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2522-869G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538682 | ||||||
| chr8:144538765
|
T | G | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2522-952A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538765 | ||||||
| chr8:144538770
|
C | T | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-957G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538770 | ||||||
| chr8:144538822
|
C | A | 9 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(6): Show | 9 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2522-1009G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538822 | ||||||
| chr8:144538835
|
T | C | 20 | a0001c0002t0001g0013a0001c0002t0001g0020a0001c0002t0001g0082others(17): Show | 20 | HG00323.hp1 HG01192.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2522-1022A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538835 | ||||||
| chr8:144538866
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2522-1053G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538866 | ||||||
| chr8:144538974
|
CCT | C | 75 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(72): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2522-1163_2522-116 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144538974 | ||||||
| chr8:144539008
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-1195G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539008 | ||||||
| chr8:144539037
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2522-1224C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539037 | ||||||
| chr8:144539099
|
T | C | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2522-1286A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539099 | ||||||
| chr8:144539160
|
C | T | 14 | a0001c0001t0003g0023a0001c0001t0004g0150a0001c0001t0004g0152others(11): Show | 14 | HG02055.hp2 HG02257.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2522-1347G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539160 | ||||||
| chr8:144539173
|
G | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-1360C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539173 | ||||||
| chr8:144539234
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-1421G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539234 | ||||||
| chr8:144539288
|
A | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-1475T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539288 | ||||||
| chr8:144539325
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-1512G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539325 | ||||||
| chr8:144539370
|
T | C | 6 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2522-1557A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539370 | ||||||
| chr8:144539416
|
C | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2522-1603G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539416 | ||||||
| chr8:144539735
|
T | A | 9 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0001t0007g0168others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2522-1922A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539735 | ||||||
| chr8:144539766
|
T | C | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2522-1953A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539766 | ||||||
| chr8:144539930
|
A | G | 11 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2522-2117T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539930 | ||||||
| chr8:144539940
|
A | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2522-2127T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144539940 | ||||||
| chr8:144540002
|
C | A | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2522-2189G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540002 | ||||||
| chr8:144540067
|
G | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-2254C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540067 | ||||||
| chr8:144540599
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2522-2786C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540599 | ||||||
| chr8:144540674
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2522-2861G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540674 | ||||||
| chr8:144540767
|
T | C | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2522-2954A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540767 | ||||||
| chr8:144540798
|
G | GA | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2522-2986dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540798 | ||||||
| chr8:144540894
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2522-3081G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144540894 | ||||||
| chr8:144541027
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2522-3214A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541027 | ||||||
| chr8:144541097
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0003g0063a0001c0001t0003g0068others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2522-3284C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541097 | ||||||
| chr8:144541106
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0008g0120a0001c0001t0008g0121others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2522-3293G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541106 | ||||||
| chr8:144541130
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2522-3317G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541130 | ||||||
| chr8:144541177
|
C | T | 1 | a0001c0003t0001g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2522-3364G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541177 | ||||||
| chr8:144541218
|
T | C | 1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2522-3405A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541218 | ||||||
| chr8:144541271
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2522-3458G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541271 | ||||||
| chr8:144541300
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0043 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2522-3487C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541300 | ||||||
| chr8:144541343
|
C | T | 6 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2522-3530G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541343 | ||||||
| chr8:144541402
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2522-3589T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541402 | ||||||
| chr8:144541510
|
C | T | 19 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(16): Show | 19 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2522-3697G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541510 | ||||||
| chr8:144541677
|
C | T | 11 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2521+3572G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541677 | ||||||
| chr8:144541678
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2521+3571C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541678 | ||||||
| chr8:144541687
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2521+3562G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541687 | ||||||
| chr8:144541815
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0197 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2521+3434C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541815 | ||||||
| chr8:144541816
|
A | G | 11 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2521+3433T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541816 | ||||||
| chr8:144541958
|
C | A | 1 | a0001c0002t0001g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2521+3291G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541958 | ||||||
| chr8:144541971
|
G | GT | 120 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0097others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.2521+3277dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541971 | ||||||
| chr8:144541971
|
G | GTT | 6 | a0001c0001t0002g0134a0001c0001t0002g0139a0001c0001t0002g0145others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2521+3276_2521+327 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541971 | ||||||
| chr8:144541971
|
GT | G | 10 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2521+3277delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144541971 | ||||||
| chr8:144542078
|
G | A | 17 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(14): Show | 17 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2521+3171C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542078 | ||||||
| chr8:144542201
|
G | C | 11 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2521+3048C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542201 | ||||||
| chr8:144542207
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2521+3042G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542207 | ||||||
| chr8:144542323
|
C | T | 1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2521+2926G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542323 | ||||||
| chr8:144542343
|
G | A | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2521+2906C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542343 | ||||||
| chr8:144542360
|
A | C | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2521+2889T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542360 | ||||||
| chr8:144542384
|
C | CGAT | 6 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2521+2862_2521+286 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542384 | ||||||
| chr8:144542649
|
G | A | 12 | a0001c0001t0001g0233a0001c0001t0004g0150a0001c0001t0004g0152others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2521+2600C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542649 | ||||||
| chr8:144542660
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2521+2589G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542660 | ||||||
| chr8:144542808
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2521+2441C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542808 | ||||||
| chr8:144542886
|
T | C | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2521+2363A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542886 | ||||||
| chr8:144542887
|
C | T | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2521+2362G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542887 | ||||||
| chr8:144542888
|
A | G | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2521+2361T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542888 | ||||||
| chr8:144542889
|
T | A | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2521+2360A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144542889 | ||||||
| chr8:144543057
|
C | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2521+2192G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543057 | ||||||
| chr8:144543189
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2521+2060A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543189 | ||||||
| chr8:144543353
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2521+1896A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543353 | ||||||
| chr8:144543357
|
A | G | 2 | a0001c0002t0001g0038a0001c0002t0001g0041 | 2 | HG02132.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2521+1892T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543357 | ||||||
| chr8:144543388
|
A | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2521+1861T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543388 | ||||||
| chr8:144543389
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2521+1860A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543389 | ||||||
| chr8:144543526
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2521+1723G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543526 | ||||||
| chr8:144543686
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2521+1563G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543686 | ||||||
| chr8:144543773
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0151 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2521+1476G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543773 | ||||||
| chr8:144543810
|
TGGCCCAA others(4): Show |
T | 15 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2521+1428_2521+143 others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543810 | ||||||
| chr8:144543991
|
G | A | 3 | a0001c0007t0001g0017a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2521+1258C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144543991 | ||||||
| chr8:144544096
|
C | T | 5 | a0001c0001t0003g0023a0001c0001t0021g0062a0001c0007t0001g0017others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2521+1153G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544096 | ||||||
| chr8:144544110
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2521+1139G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544110 | ||||||
| chr8:144544352
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2521+897C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544352 | ||||||
| chr8:144544453
|
T | A | 3 | a0001c0007t0001g0017a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2521+796A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544453 | ||||||
| chr8:144544475
|
C | T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2521+774G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544475 | ||||||
| chr8:144544501
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0001t0007g0168others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2521+748G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544501 | ||||||
| chr8:144544513
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2521+736C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544513 | ||||||
| chr8:144544538
|
G | A | 1 | a0001c0001t0005g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2521+711C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544538 | ||||||
| chr8:144544562
|
A | AGAGCTGC others(156): Show |
1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2521+524_2521+686d others(165): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544562 | ||||||
| chr8:144544567
|
T | G | 47 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(44): Show | 47 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(44): Show |
intron_variant | MODIFIER | c.2521+682A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544567 | ||||||
| chr8:144544671
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2521+578G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544671 | ||||||
| chr8:144544672
|
G | A | 6 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2521+577C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544672 | ||||||
| chr8:144544705
|
G | A | 4 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2521+544C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544705 | ||||||
| chr8:144544800
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2521+449C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544800 | ||||||
| chr8:144544857
|
G | A | 3 | a0001c0007t0001g0017a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2521+392C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544857 | ||||||
| chr8:144544907
|
C | A | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0099 | 3 | HG00280.hp2 HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2521+342G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544907 | ||||||
| chr8:144544915
|
C | T | 2 | a0001c0001t0001g0209a0001c0002t0001g0137 | 2 | NA18946.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2521+334G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544915 | ||||||
| chr8:144544998
|
C | T | 14 | a0001c0001t0001g0238a0001c0002t0001g0035a0001c0002t0001g0090others(11): Show | 14 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.2521+251G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144544998 | ||||||
| chr8:144545011
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0002g0241 | 2 | HG01975.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2521+238G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144545011 | ||||||
| chr8:144545017
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2521+232G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144545017 | ||||||
| chr8:144545042
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2521+207C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144545042 | ||||||
| chr8:144545169
|
A | G | 37 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(34): Show | 37 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2521+80T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | 144545169 | ||||||
| chr8:144545827
|
C | G | 140 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(137): Show | 140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1960-17G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144545827 | ||||||
| chr8:144545881
|
AG | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0223others(18): Show | 21 | HG01891.hp1 HG01975.hp2 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.1960-72delC | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144545881 | ||||||
| chr8:144545886
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1960-76G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144545886 | ||||||
| chr8:144546083
|
A | G | 10 | a0001c0001t0002g0138a0001c0001t0002g0241a0001c0001t0004g0150others(7): Show | 10 | HG01975.hp2 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1960-273T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546083 | ||||||
| chr8:144546113
|
C | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1960-303G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546113 | ||||||
| chr8:144546242
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1960-432G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546242 | ||||||
| chr8:144546345
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1960-535G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546345 | ||||||
| chr8:144546529
|
T | G | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1959+598A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546529 | ||||||
| chr8:144546618
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1959+509G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546618 | ||||||
| chr8:144546646
|
G | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1959+481C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546646 | ||||||
| chr8:144546690
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1959+437C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546690 | ||||||
| chr8:144546706
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1959+421G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546706 | ||||||
| chr8:144546718
|
G | A | 2 | a0001c0007t0003g0078a0001c0007t0017g0019 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1959+409C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546718 | ||||||
| chr8:144546733
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959+394C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546733 | ||||||
| chr8:144546751
|
C | T | 3 | a0001c0001t0018g0022a0001c0002t0001g0098a0001c0002t0019g0125 | 3 | HG02258.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1959+376G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546751 | ||||||
| chr8:144546790
|
G | A | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1959+337C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546790 | ||||||
| chr8:144546796
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959+331C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546796 | ||||||
| chr8:144546873
|
G | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959+254C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546873 | ||||||
| chr8:144546941
|
G | A | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1959+186C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144546941 | ||||||
| chr8:144547115
|
T | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1959+12A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 5/11 | chr8 | 144547115 | ||||||
| chr8:144548726
|
G | C | 1 | a0004c0009t0001g0008 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.597-237C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144548726 | ||||||
| chr8:144548834
|
G | T | 1 | a0001c0003t0009g0004 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.597-345C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144548834 | ||||||
| chr8:144548903
|
C | T | 36 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(33): Show | 36 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.597-414G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144548903 | ||||||
| chr8:144548940
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597-451G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144548940 | ||||||
| chr8:144548995
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-506G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144548995 | ||||||
| chr8:144549180
|
C | T | 9 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0001t0007g0239others(6): Show | 9 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.597-691G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549180 | ||||||
| chr8:144549186
|
A | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.597-697T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549186 | ||||||
| chr8:144549225
|
G | T | 1 | a0001c0002t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.597-736C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549225 | ||||||
| chr8:144549529
|
T | C | 3 | a0001c0007t0001g0017a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.597-1040A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549529 | ||||||
| chr8:144549551
|
G | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(19): Show | 22 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.597-1062C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549551 | ||||||
| chr8:144549648
|
A | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-1159T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549648 | ||||||
| chr8:144549695
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.597-1206C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549695 | ||||||
| chr8:144549735
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.597-1246G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549735 | ||||||
| chr8:144549782
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.597-1293G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144549782 | ||||||
| chr8:144550010
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-1521G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550010 | ||||||
| chr8:144550131
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.597-1642C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550131 | ||||||
| chr8:144550265
|
A | G | 4 | a0001c0007t0001g0017a0001c0007t0003g0078a0001c0007t0017g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-1776T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550265 | ||||||
| chr8:144550486
|
T | C | 12 | a0001c0001t0016g0105a0001c0003t0001g0005a0001c0003t0001g0012others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.597-1997A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550486 | ||||||
| chr8:144550544
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.597-2055C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550544 | ||||||
| chr8:144550544
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.597-2055C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550544 | ||||||
| chr8:144550638
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-2149G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550638 | ||||||
| chr8:144550896
|
G | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-2407C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550896 | ||||||
| chr8:144550971
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-2482C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144550971 | ||||||
| chr8:144551010
|
A | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.597-2521T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551010 | ||||||
| chr8:144551380
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.597-2891T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551380 | ||||||
| chr8:144551385
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.597-2896C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551385 | ||||||
| chr8:144551392
|
C | A | 18 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(15): Show | 18 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.597-2903G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551392 | ||||||
| chr8:144551474
|
C | T | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.597-2985G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551474 | ||||||
| chr8:144551508
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.597-3019G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551508 | ||||||
| chr8:144551626
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.597-3137C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551626 | ||||||
| chr8:144551831
|
C | T | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.597-3342G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551831 | ||||||
| chr8:144551872
|
C | T | 15 | a0001c0001t0016g0105a0001c0003t0001g0005a0001c0003t0001g0012others(12): Show | 15 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-3383G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144551872 | ||||||
| chr8:144552117
|
AG | A | 3 | a0001c0001t0007g0018a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02451.hp2 HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.596+3442delC | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552117 | ||||||
| chr8:144552206
|
C | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.596+3354G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552206 | ||||||
| chr8:144552222
|
G | A | 20 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(17): Show | 20 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.596+3338C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552222 | ||||||
| chr8:144552250
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.596+3310G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552250 | ||||||
| chr8:144552281
|
C | CAAAGCAA others(24): Show |
1 | a0001c0001t0001g0033 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.596+3248_596+3278d others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552281 | ||||||
| chr8:144552397
|
C | T | 3 | a0001c0001t0007g0018a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02451.hp2 HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.596+3163G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552397 | ||||||
| chr8:144552398
|
G | A | 2 | a0001c0002t0001g0140a0001c0002t0001g0222 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.596+3162C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552398 | ||||||
| chr8:144552400
|
C | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.596+3160G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552400 | ||||||
| chr8:144552717
|
T | C | 68 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0100others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.596+2843A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552717 | ||||||
| chr8:144552744
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0097a0001c0001t0001g0151others(36): Show | 39 | HG00280.hp1 HG00408.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.596+2816G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552744 | ||||||
| chr8:144552820
|
G | A | 4 | a0001c0004t0006g0070a0001c0004t0006g0073a0001c0004t0006g0074others(1): Show | 4 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+2740C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552820 | ||||||
| chr8:144552963
|
T | C | 181 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.596+2597A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144552963 | ||||||
| chr8:144553032
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.596+2528A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553032 | ||||||
| chr8:144553089
|
A | T | 30 | a0001c0001t0001g0122a0001c0001t0001g0148a0001c0001t0001g0149others(27): Show | 30 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.596+2471T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553089 | ||||||
| chr8:144553248
|
C | T | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.596+2312G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553248 | ||||||
| chr8:144553331
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.596+2229C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553331 | ||||||
| chr8:144553427
|
C | T | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.596+2133G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553427 | ||||||
| chr8:144553431
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.596+2129G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553431 | ||||||
| chr8:144553520
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.596+2040A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553520 | ||||||
| chr8:144553534
|
C | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0238others(14): Show | 17 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+2026G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553534 | ||||||
| chr8:144553595
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.596+1965C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553595 | ||||||
| chr8:144553792
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.596+1768G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553792 | ||||||
| chr8:144553824
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.596+1736G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553824 | ||||||
| chr8:144553831
|
C | T | 1 | a0001c0002t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.596+1729G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553831 | ||||||
| chr8:144553855
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.596+1705G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553855 | ||||||
| chr8:144553869
|
G | A | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+1691C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553869 | ||||||
| chr8:144553926
|
G | A | 1 | a0001c0015t0001g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.596+1634C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553926 | ||||||
| chr8:144553991
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.596+1569C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144553991 | ||||||
| chr8:144554043
|
G | T | 28 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(25): Show | 28 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.596+1517C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554043 | ||||||
| chr8:144554055
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.596+1505C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554055 | ||||||
| chr8:144554128
|
G | A | 2 | a0001c0001t0008g0121a0001c0001t0008g0166 | 2 | HG02145.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.596+1432C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554128 | ||||||
| chr8:144554171
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.596+1389A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554171 | ||||||
| chr8:144554269
|
A | G | 3 | a0001c0002t0001g0126a0001c0002t0001g0169a0001c0007t0017g0019 | 3 | HG01192.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.596+1291T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554269 | ||||||
| chr8:144554327
|
G | C | 7 | a0001c0001t0002g0139a0001c0001t0002g0170a0001c0004t0006g0069others(4): Show | 7 | HG02280.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+1233C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554327 | ||||||
| chr8:144554379
|
T | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.596+1181A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554379 | ||||||
| chr8:144554422
|
A | C | 54 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0151others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.596+1138T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554422 | ||||||
| chr8:144554512
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0002g0170 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.596+1048C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554512 | ||||||
| chr8:144554829
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596+731C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554829 | ||||||
| chr8:144554887
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.596+673C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554887 | ||||||
| chr8:144554939
|
C | T | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.596+621G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144554939 | ||||||
| chr8:144555116
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.596+444C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144555116 | ||||||
| chr8:144555368
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.596+192G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4/11 | chr8 | 144555368 | ||||||
| chr8:144555687
|
C | T | 7 | a0001c0001t0002g0131a0001c0002t0001g0020a0001c0002t0001g0082others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-44G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144555687 | ||||||
| chr8:144555704
|
C | T | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.513-61G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144555704 | ||||||
| chr8:144556005
|
A | G | 49 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.513-362T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556005 | ||||||
| chr8:144556056
|
C | T | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513-413G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556056 | ||||||
| chr8:144556157
|
C | T | 1 | a0004c0009t0001g0008 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.513-514G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556157 | ||||||
| chr8:144556234
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-591C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556234 | ||||||
| chr8:144556241
|
C | T | 57 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0097others(54): Show | 57 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.513-598G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556241 | ||||||
| chr8:144556283
|
T | TA | 13 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0143others(10): Show | 13 | HG01081.hp1 HG02055.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.513-641dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556283 | ||||||
| chr8:144556283
|
TA | T | 38 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0203others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.513-641delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556283 | ||||||
| chr8:144556313
|
C | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-670G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556313 | ||||||
| chr8:144556326
|
G | A | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513-683C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556326 | ||||||
| chr8:144556396
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-753G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556396 | ||||||
| chr8:144556416
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-773C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556416 | ||||||
| chr8:144556428
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.513-785T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556428 | ||||||
| chr8:144556546
|
C | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-903G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556546 | ||||||
| chr8:144556587
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-944T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556587 | ||||||
| chr8:144556598
|
A | AGGCAAAG others(23): Show |
9 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(6): Show | 9 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.513-956_513-955ins others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556598 | ||||||
| chr8:144556606
|
GCTGAACC others(23): Show |
G | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0007t0003g0078 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-993_513-964del others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556606 | ||||||
| chr8:144556617
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-974T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556617 | ||||||
| chr8:144556628
|
A | T | 36 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(33): Show | 36 | HG01952.hp1 HG02055.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.513-985T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556628 | ||||||
| chr8:144556636
|
C | G | 47 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.513-993G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556636 | ||||||
| chr8:144556647
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1004T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556647 | ||||||
| chr8:144556649
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.513-1006T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556649 | ||||||
| chr8:144556651
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.513-1008A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556651 | ||||||
| chr8:144556658
|
A | T | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0007t0003g0078 | 3 | HG02257.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1015T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556658 | ||||||
| chr8:144556661
|
C | CA | 9 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(6): Show | 9 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.513-1019dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556661 | ||||||
| chr8:144556661
|
C | CAAAGGCT others(24): Show |
1 | a0001c0005t0001g0010 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.513-1049_513-1019d others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556661 | ||||||
| chr8:144556666
|
G | C | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1023C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556666 | ||||||
| chr8:144556672
|
C | A | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-1029G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556672 | ||||||
| chr8:144556677
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1034T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556677 | ||||||
| chr8:144556691
|
CA | C | 6 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0002t0001g0025others(3): Show | 6 | HG01358.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-1049delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556691 | ||||||
| chr8:144556697
|
G | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1054C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556697 | ||||||
| chr8:144556708
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1065T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556708 | ||||||
| chr8:144556722
|
CA | C | 3 | a0001c0001t0007g0018a0001c0002t0001g0164a0001c0007t0001g0017 | 3 | HG01358.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1080delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556722 | ||||||
| chr8:144556728
|
G | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1085C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556728 | ||||||
| chr8:144556753
|
C | CA | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0002t0001g0108 | 3 | HG03041.hp1 NA19043.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.513-1111dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556753 | ||||||
| chr8:144556753
|
C | CAAAGGCT others(116): Show |
2 | a0001c0002t0001g0140a0001c0002t0001g0222 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.513-1233_513-1111d others(125): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556753 | ||||||
| chr8:144556758
|
G | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1115C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556758 | ||||||
| chr8:144556771
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1128T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556771 | ||||||
| chr8:144556780
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1137T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556780 | ||||||
| chr8:144556780
|
A | T | 1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.513-1137T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556780 | ||||||
| chr8:144556783
|
CA | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(29): Show | 32 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.513-1141delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556783 | ||||||
| chr8:144556784
|
A | AAAAGCCT others(53): Show |
1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.513-1142_513-1141i others(62): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556784 | ||||||
| chr8:144556789
|
G | C | 29 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(26): Show | 29 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.513-1146C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556789 | ||||||
| chr8:144556801
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1158A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556801 | ||||||
| chr8:144556811
|
A | C | 3 | a0001c0001t0007g0018a0001c0002t0001g0108a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.513-1168T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556811 | ||||||
| chr8:144556812
|
G | T | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1169C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556812 | ||||||
| chr8:144556814
|
CA | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(32): Show | 35 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.513-1172delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556814 | ||||||
| chr8:144556820
|
G | C | 4 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0002t0001g0108others(1): Show | 4 | HG01358.hp2 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1177C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556820 | ||||||
| chr8:144556827
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1184G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556827 | ||||||
| chr8:144556831
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1188T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556831 | ||||||
| chr8:144556837
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.513-1194A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556837 | ||||||
| chr8:144556842
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1199T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556842 | ||||||
| chr8:144556845
|
C | CA | 13 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.513-1203dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556845 | ||||||
| chr8:144556850
|
G | C | 27 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-1207C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556850 | ||||||
| chr8:144556861
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1218T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556861 | ||||||
| chr8:144556872
|
A | T | 11 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-1229T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556872 | ||||||
| chr8:144556875
|
CA | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(29): Show | 32 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(29): Show |
intron_variant | MODIFIER | c.513-1233delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556875 | ||||||
| chr8:144556876
|
A | AAAGGCTG others(83): Show |
5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1234_513-1233i others(92): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556876 | ||||||
| chr8:144556881
|
G | C | 34 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(31): Show | 34 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.513-1238C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556881 | ||||||
| chr8:144556892
|
A | G | 3 | a0001c0001t0007g0018a0001c0002t0001g0164a0001c0007t0001g0017 | 3 | HG01358.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1249T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556892 | ||||||
| chr8:144556903
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1260T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556903 | ||||||
| chr8:144556906
|
CA | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(32): Show | 35 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.513-1264delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556906 | ||||||
| chr8:144556912
|
G | C | 29 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(26): Show | 29 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(26): Show |
intron_variant | MODIFIER | c.513-1269C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556912 | ||||||
| chr8:144556923
|
A | G | 14 | a0001c0001t0007g0018a0001c0002t0001g0013a0001c0002t0001g0106others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-1280T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556923 | ||||||
| chr8:144556927
|
T | C | 12 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-1284A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556927 | ||||||
| chr8:144556934
|
A | C | 29 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(26): Show | 29 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.513-1291T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556934 | ||||||
| chr8:144556934
|
A | T | 12 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-1291T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556934 | ||||||
| chr8:144556934
|
AGGCAAAA others(327): Show |
A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1625_513-1292d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556934 | ||||||
| chr8:144556937
|
CA | C | 12 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0108others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-1295delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556937 | ||||||
| chr8:144556937
|
CAAAAGGC others(116): Show |
C | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1417_513-1295d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556937 | ||||||
| chr8:144556938
|
A | AAAAGCCT others(53): Show |
5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1296_513-1295i others(62): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556938 | ||||||
| chr8:144556943
|
G | C | 2 | a0001c0001t0020g0079a0001c0006t0001g0193 | 2 | HG01081.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.513-1300C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556943 | ||||||
| chr8:144556950
|
C | T | 27 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-1307G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556950 | ||||||
| chr8:144556954
|
A | G | 38 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(35): Show | 38 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.513-1311T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556954 | ||||||
| chr8:144556956
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1313T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556956 | ||||||
| chr8:144556965
|
T | A | 9 | a0001c0001t0007g0018a0001c0001t0020g0079a0001c0002t0001g0108others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-1322A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556965 | ||||||
| chr8:144556965
|
T | C | 38 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(35): Show | 38 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.513-1322A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556965 | ||||||
| chr8:144556968
|
CA | C | 9 | a0001c0001t0007g0018a0001c0001t0020g0079a0001c0002t0001g0108others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-1326delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556968 | ||||||
| chr8:144556974
|
C | G | 41 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(38): Show | 41 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.513-1331G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556974 | ||||||
| chr8:144556985
|
A | G | 38 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(35): Show | 38 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.513-1342T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556985 | ||||||
| chr8:144556991
|
T | C | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG01952.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-1348A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556991 | ||||||
| chr8:144556996
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1353T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556996 | ||||||
| chr8:144556996
|
A | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513-1353T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144556996 | ||||||
| chr8:144557015
|
A | G | 40 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(37): Show | 40 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.513-1372T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557015 | ||||||
| chr8:144557026
|
T | A | 11 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-1383A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557026 | ||||||
| chr8:144557026
|
T | C | 3 | a0001c0001t0007g0018a0001c0001t0020g0079a0001c0007t0001g0017 | 3 | HG02109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1383A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557026 | ||||||
| chr8:144557029
|
C | CA | 30 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(27): Show | 30 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.513-1387dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557029 | ||||||
| chr8:144557034
|
G | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513-1391C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557034 | ||||||
| chr8:144557045
|
A | G | 40 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(37): Show | 40 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.513-1402T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557045 | ||||||
| chr8:144557051
|
T | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513-1408A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557051 | ||||||
| chr8:144557056
|
C | A | 9 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(6): Show | 9 | HG01891.hp1 HG01952.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-1413G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557056 | ||||||
| chr8:144557056
|
C | T | 5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1413G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557056 | ||||||
| chr8:144557059
|
CA | C | 3 | a0001c0001t0007g0018a0001c0001t0020g0079a0001c0007t0001g0017 | 3 | HG02109.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1417delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557059 | ||||||
| chr8:144557065
|
C | G | 45 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(42): Show | 45 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.513-1422G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557065 | ||||||
| chr8:144557076
|
A | G | 19 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.513-1433T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557076 | ||||||
| chr8:144557078
|
A | C | 27 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-1435T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557078 | ||||||
| chr8:144557082
|
C | T | 48 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(45): Show | 48 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.513-1439G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557082 | ||||||
| chr8:144557090
|
C | CAAAGCCT others(144): Show |
5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1448_513-1447i others(153): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557090 | ||||||
| chr8:144557095
|
G | C | 5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1452C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557095 | ||||||
| chr8:144557095
|
G | GCTGAACC others(721): Show |
1 | a0001c0005t0001g0010 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.513-1453_513-1452i others(730): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557095 | ||||||
| chr8:144557106
|
A | G | 14 | a0001c0001t0001g0228a0001c0001t0003g0063a0001c0001t0003g0068others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-1463T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557106 | ||||||
| chr8:144557117
|
A | C | 27 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-1474T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557117 | ||||||
| chr8:144557120
|
C | CA | 28 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(25): Show | 28 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.513-1478dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557120 | ||||||
| chr8:144557136
|
A | G | 39 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(36): Show | 39 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.513-1493T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557136 | ||||||
| chr8:144557147
|
A | C | 27 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-1504T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557147 | ||||||
| chr8:144557147
|
A | T | 15 | a0001c0001t0007g0018a0001c0002t0001g0013a0001c0002t0001g0106others(12): Show | 15 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.513-1504T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557147 | ||||||
| chr8:144557150
|
CA | C | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-1508delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557150 | ||||||
| chr8:144557167
|
G | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.513-1524C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557167 | ||||||
| chr8:144557167
|
G | C | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1524C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557167 | ||||||
| chr8:144557186
|
G | C | 33 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(30): Show | 33 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(30): Show |
intron_variant | MODIFIER | c.513-1543C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557186 | ||||||
| chr8:144557197
|
G | A | 3 | a0001c0001t0007g0018a0001c0002t0001g0164a0001c0007t0001g0017 | 3 | HG01358.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1554C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557197 | ||||||
| chr8:144557215
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-1572C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557215 | ||||||
| chr8:144557216
|
G | C | 13 | a0001c0001t0007g0018a0001c0002t0001g0013a0001c0002t0001g0106others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.513-1573C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557216 | ||||||
| chr8:144557227
|
G | A | 9 | a0001c0001t0007g0018a0001c0002t0001g0013a0001c0002t0001g0106others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-1584C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557227 | ||||||
| chr8:144557238
|
A | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-1595T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557238 | ||||||
| chr8:144557257
|
G | A | 42 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(39): Show | 42 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.513-1614C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557257 | ||||||
| chr8:144557268
|
T | A | 14 | a0001c0001t0007g0018a0001c0002t0001g0013a0001c0002t0001g0106others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-1625A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557268 | ||||||
| chr8:144557268
|
T | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.513-1625A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557268 | ||||||
| chr8:144557271
|
C | CA | 28 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(25): Show | 28 | HG01952.hp1 HG02055.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.513-1629dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557271 | ||||||
| chr8:144557271
|
C | CAAAAGGC others(55): Show |
1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-1629_513-1628i others(64): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557271 | ||||||
| chr8:144557271
|
CAAAGGCT others(24): Show |
C | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.513-1659_513-1629d others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557271 | ||||||
| chr8:144557276
|
G | C | 4 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0002t0001g0025others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1633C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557276 | ||||||
| chr8:144557287
|
G | A | 15 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0002t0001g0013others(12): Show | 15 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.513-1644C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557287 | ||||||
| chr8:144557289
|
A | G | 6 | a0001c0002t0001g0108a0001c0004t0006g0069a0001c0004t0006g0070others(3): Show | 6 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-1646T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557289 | ||||||
| chr8:144557298
|
C | A | 36 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(33): Show | 36 | HG01952.hp1 HG02055.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.513-1655G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557298 | ||||||
| chr8:144557298
|
C | T | 5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1655G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557298 | ||||||
| chr8:144557301
|
CA | C | 3 | a0001c0001t0007g0018a0001c0005t0001g0010a0001c0007t0001g0017 | 3 | HG01952.hp1 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1659delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557301 | ||||||
| chr8:144557302
|
A | AAAGGCTG others(355): Show |
1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.513-1660_513-1659i others(364): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557302 | ||||||
| chr8:144557302
|
A | AAAGGCTG others(82): Show |
3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.513-1660_513-1659i others(91): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557302 | ||||||
| chr8:144557302
|
A | AAAGGCTG others(82): Show |
24 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(21): Show | 24 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.513-1660_513-1659i others(91): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557302 | ||||||
| chr8:144557302
|
A | AAAGGCTG others(355): Show |
5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1660_513-1659i others(364): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557302 | ||||||
| chr8:144557307
|
G | C | 37 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(34): Show | 37 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(34): Show |
intron_variant | MODIFIER | c.513-1664C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557307 | ||||||
| chr8:144557314
|
C | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1671G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557314 | ||||||
| chr8:144557318
|
G | A | 43 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(40): Show | 43 | HG00408.hp2 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.513-1675C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557318 | ||||||
| chr8:144557318
|
G | C | 5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1675C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557318 | ||||||
| chr8:144557329
|
A | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1686T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557329 | ||||||
| chr8:144557337
|
G | C | 37 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(34): Show | 37 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.513-1694C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557337 | ||||||
| chr8:144557337
|
G | GCTGAACC others(113): Show |
5 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0111others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1695_513-1694i others(122): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557337 | ||||||
| chr8:144557348
|
G | A | 41 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(38): Show | 41 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.513-1705C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557348
|
G | GTAGTATT others(810): Show |
1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-1706_513-1705i others(819): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557348
|
G | GTAGTATT others(902): Show |
1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-1706_513-1705i others(911): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557348
|
G | GTAGTATT others(902): Show |
8 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0009g0004others(5): Show | 8 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.513-1706_513-1705i others(911): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557348
|
G | GTAGTATT others(902): Show |
1 | a0001c0003t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.513-1706_513-1705i others(911): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557348
|
G | GTAGTATT others(902): Show |
1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-1706_513-1705i others(911): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557348 | ||||||
| chr8:144557359
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1716T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557359 | ||||||
| chr8:144557367
|
G | C | 51 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.513-1724C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(83): Show |
1 | a0001c0005t0001g0010 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.513-1725_513-1724i others(92): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(476): Show |
1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.513-1725_513-1724i others(485): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(446): Show |
1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.513-1725_513-1724i others(455): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(537): Show |
1 | a0001c0001t0001g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.513-1725_513-1724i others(546): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
165 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
4 | a0001c0002t0001g0093a0001c0002t0001g0119a0001c0002t0001g0147others(1): Show | 4 | HG01099.hp1 HG01981.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
3 | a0001c0001t0002g0139a0001c0001t0002g0170a0001c0001t0020g0079 | 3 | HG02109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0203 | 3 | HG02717.hp2 HG02735.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(597): Show |
1 | a0001c0002t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.513-1725_513-1724i others(606): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557367
|
G | GCTGAACC others(627): Show |
1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.513-1725_513-1724i others(636): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557367 | ||||||
| chr8:144557374
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1731G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557374 | ||||||
| chr8:144557378
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0007g0018a0001c0002t0001g0025others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1735T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557378 | ||||||
| chr8:144557389
|
T | C | 42 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(39): Show | 42 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.513-1746A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557389 | ||||||
| chr8:144557405
|
C | T | 31 | a0001c0001t0001g0151a0001c0001t0001g0228a0001c0001t0003g0023others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.513-1762G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557405 | ||||||
| chr8:144557420
|
C | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1777G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557420 | ||||||
| chr8:144557440
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1797C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557440 | ||||||
| chr8:144557442
|
A | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1799T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557442 | ||||||
| chr8:144557451
|
A | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1808T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557451 | ||||||
| chr8:144557457
|
A | G | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.513-1814T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557457 | ||||||
| chr8:144557470
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1827C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557470 | ||||||
| chr8:144557481
|
T | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0007g0018others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-1838A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557481 | ||||||
| chr8:144557485
|
AAAAGGCT others(54): Show |
A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-1903_513-1843d others(63): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557485 | ||||||
| chr8:144557501
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1858C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557501 | ||||||
| chr8:144557503
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1860T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557503 | ||||||
| chr8:144557512
|
C | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1869G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557512 | ||||||
| chr8:144557534
|
C | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1891G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557534 | ||||||
| chr8:144557543
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-1900T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557543 | ||||||
| chr8:144557546
|
C | CAAAGGCT others(24): Show |
39 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(36): Show | 39 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.513-1934_513-1904d others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557546 | ||||||
| chr8:144557562
|
A | ATAGTATT others(24): Show |
1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-1950_513-1920d others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557562 | ||||||
| chr8:144557593
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-1950C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557593 | ||||||
| chr8:144557683
|
A | G | 3 | a0001c0001t0007g0018a0001c0007t0001g0017a0004c0009t0001g0008 | 3 | HG00408.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-2040T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557683 | ||||||
| chr8:144557748
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.513-2105A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557748 | ||||||
| chr8:144557775
|
G | A | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2132C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557775 | ||||||
| chr8:144557781
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0241 | 2 | HG01975.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.513-2138A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557781 | ||||||
| chr8:144557841
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.513-2198T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557841 | ||||||
| chr8:144557881
|
T | C | 1 | a0001c0001t0004g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.513-2238A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557881 | ||||||
| chr8:144557903
|
C | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-2260G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144557903 | ||||||
| chr8:144558013
|
ACTTACGT others(17): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-2394_513-2371d others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558013 | ||||||
| chr8:144558177
|
A | G | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2534T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558177 | ||||||
| chr8:144558209
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.513-2566G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558209 | ||||||
| chr8:144558281
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.513-2638T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558281 | ||||||
| chr8:144558338
|
A | G | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2695T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558338 | ||||||
| chr8:144558373
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-2730T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558373 | ||||||
| chr8:144558475
|
T | G | 10 | a0001c0001t0002g0134a0001c0001t0002g0138a0001c0001t0002g0139others(7): Show | 10 | HG01975.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-2832A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558475 | ||||||
| chr8:144558492
|
C | A | 1 | a0001c0001t0002g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.513-2849G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558492 | ||||||
| chr8:144558513
|
G | A | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2870C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558513 | ||||||
| chr8:144558537
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.513-2894G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558537 | ||||||
| chr8:144558568
|
C | G | 1 | a0001c0001t0002g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.513-2925G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558568 | ||||||
| chr8:144558593
|
A | AT | 201 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.513-2951dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558593 | ||||||
| chr8:144558594
|
T | TG | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2952_513-2951i others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558594 | ||||||
| chr8:144558595
|
A | G | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-2952T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558595 | ||||||
| chr8:144558933
|
G | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-3290C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558933 | ||||||
| chr8:144558961
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0043 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.513-3318G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144558961 | ||||||
| chr8:144559195
|
G | A | 4 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-3552C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559195 | ||||||
| chr8:144559218
|
A | G | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-3575T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559218 | ||||||
| chr8:144559276
|
G | A | 13 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.513-3633C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559276 | ||||||
| chr8:144559340
|
A | G | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-3697T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559340 | ||||||
| chr8:144559354
|
C | CA | 24 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0223others(21): Show | 24 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.513-3712dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
C | CAA | 12 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0224others(9): Show | 12 | HG02055.hp2 HG02145.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-3713_513-3712d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
C | CAAA | 6 | a0001c0001t0001g0238a0001c0001t0004g0237a0001c0001t0007g0239others(3): Show | 6 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-3714_513-3712d others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
CA | C | 39 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.513-3712delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
CAA | C | 74 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(71): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.513-3713_513-3712d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
CAAA | C | 5 | a0001c0001t0001g0236a0001c0001t0005g0187a0001c0001t0020g0079others(2): Show | 5 | HG00558.hp2 HG00639.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-3714_513-3712d others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513-3721_513-3712d others(12): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559354
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-3727_513-3712d others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559354 | ||||||
| chr8:144559599
|
C | T | 1 | a0001c0002t0019g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.513-3956G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559599 | ||||||
| chr8:144559625
|
C | T | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-3982G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559625 | ||||||
| chr8:144559827
|
C | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-4184G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559827 | ||||||
| chr8:144559920
|
C | T | 3 | a0001c0001t0001g0050a0001c0002t0001g0140a0001c0002t0001g0222 | 3 | HG00408.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.513-4277G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559920 | ||||||
| chr8:144559947
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | NA18963.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.513-4304C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144559947 | ||||||
| chr8:144560155
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-4512G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560155 | ||||||
| chr8:144560161
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-4518G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560161 | ||||||
| chr8:144560162
|
A | G | 44 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(41): Show | 44 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.513-4519T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560162 | ||||||
| chr8:144560251
|
T | G | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-4608A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560251 | ||||||
| chr8:144560263
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513-4620G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560263 | ||||||
| chr8:144560292
|
G | A | 2 | a0001c0004t0006g0069a0001c0004t0006g0070 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.513-4649C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560292 | ||||||
| chr8:144560304
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0007g0018a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.513-4661C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560304 | ||||||
| chr8:144560381
|
GCTGGGAT others(1): Show |
G | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-4746_513-4739d others(10): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560381 | ||||||
| chr8:144560400
|
A | G | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-4757T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560400 | ||||||
| chr8:144560429
|
C | T | 3 | a0001c0001t0003g0063a0001c0001t0003g0071a0001c0001t0003g0076 | 3 | HG02895.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.513-4786G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560429 | ||||||
| chr8:144560452
|
T | G | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-4809A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560452 | ||||||
| chr8:144560514
|
C | T | 1 | a0001c0001t0004g0156 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.513-4871G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560514 | ||||||
| chr8:144560690
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.513-5047G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560690 | ||||||
| chr8:144560767
|
G | A | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-5124C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560767 | ||||||
| chr8:144560800
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-5157G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560800 | ||||||
| chr8:144560918
|
A | G | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.513-5275T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144560918 | ||||||
| chr8:144561024
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513-5381C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561024 | ||||||
| chr8:144561134
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.513-5491A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561134 | ||||||
| chr8:144561145
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-5502G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561145 | ||||||
| chr8:144561253
|
GTCCATCA others(13): Show |
G | 34 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(31): Show | 34 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.513-5630_513-5611d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561253 | ||||||
| chr8:144561261
|
G | C | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-5618C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561261 | ||||||
| chr8:144561264
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-5621G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561264 | ||||||
| chr8:144561264
|
CCCAGTGG others(13): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.513-5641_513-5622d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561264 | ||||||
| chr8:144561273
|
T | G | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-5630A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561273 | ||||||
| chr8:144561303
|
T | C | 57 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0151others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.513-5660A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561303 | ||||||
| chr8:144561388
|
CCCAGTGG others(33): Show |
C | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-5785_513-5746d others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561388 | ||||||
| chr8:144561397
|
G | T | 39 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(36): Show | 39 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(36): Show |
intron_variant | MODIFIER | c.513-5754C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561397 | ||||||
| chr8:144561397
|
GTCCATCA others(13): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.513-5774_513-5755d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561397 | ||||||
| chr8:144561437
|
G | T | 15 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(12): Show | 15 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.513-5794C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561437 | ||||||
| chr8:144561437
|
GTCCATCA others(13): Show |
G | 15 | a0001c0001t0002g0131a0001c0001t0004g0237a0001c0001t0007g0168others(12): Show | 15 | HG00323.hp1 HG01192.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.513-5814_513-5795d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561437 | ||||||
| chr8:144561457
|
T | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-5814A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561457 | ||||||
| chr8:144561457
|
T | TTCCATCA others(13): Show |
1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.513-5815_513-5814i others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561457 | ||||||
| chr8:144561485
|
C | G | 3 | a0001c0002t0001g0117a0001c0002t0001g0218a0005c0013t0002g0195 | 3 | HG02145.hp2 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.513-5842G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561485 | ||||||
| chr8:144561500
|
C | G | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513-5857G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561500 | ||||||
| chr8:144561504
|
A | G | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513-5861T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561504 | ||||||
| chr8:144561506
|
ACTCCAGT others(93): Show |
A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513-5963_513-5864d others(102): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561506 | ||||||
| chr8:144561508
|
T | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.513-5865A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561508 | ||||||
| chr8:144561568
|
CCCAGTGG others(33): Show |
C | 69 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0097others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.513-5965_513-5926d others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561568 | ||||||
| chr8:144561608
|
T | C | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513-5965A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561608 | ||||||
| chr8:144561624
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-5981C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561624 | ||||||
| chr8:144561625
|
G | C | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0016t0001g0091 | 3 | HG01081.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-5982C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561625 | ||||||
| chr8:144561626
|
A | G | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0016t0001g0091 | 3 | HG01081.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-5983T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561626 | ||||||
| chr8:144561628
|
C | T | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0016t0001g0091 | 3 | HG01081.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513-5985G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561628 | ||||||
| chr8:144561628
|
CCCAGTGG others(13): Show |
C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-6005_513-5986d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561628 | ||||||
| chr8:144561644
|
G | A | 3 | a0001c0001t0007g0018a0001c0002t0001g0117a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.513-6001C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561644 | ||||||
| chr8:144561663
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-6020G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561663 | ||||||
| chr8:144561664
|
G | A | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-6021C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561664 | ||||||
| chr8:144561665
|
CGCTCCAG others(57): Show |
C | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-6086_513-6023d others(66): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561665 | ||||||
| chr8:144561704
|
A | G | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-6061T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561704 | ||||||
| chr8:144561705
|
C | CGCTCCAG others(37): Show |
9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-6063_513-6062i others(46): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561705 | ||||||
| chr8:144561706
|
A | G | 8 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0005g0187others(5): Show | 8 | HG00323.hp2 HG00558.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-6063T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561706 | ||||||
| chr8:144561707
|
C | A | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-6064G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561707 | ||||||
| chr8:144561707
|
C | CTCCAGTG others(177): Show |
2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-6065_513-6064i others(186): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561707 | ||||||
| chr8:144561707
|
CTCCAGTG others(17): Show |
C | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513-6088_513-6065d others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561707 | ||||||
| chr8:144561724
|
G | A | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-6081C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561724 | ||||||
| chr8:144561731
|
A | C | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-6088T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561731 | ||||||
| chr8:144561747
|
C | T | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-6104G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561747 | ||||||
| chr8:144561755
|
A | ATCCAGTG others(17): Show |
6 | a0001c0001t0001g0228a0001c0001t0003g0023a0001c0001t0004g0237others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-6113_513-6112i others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561755 | ||||||
| chr8:144561755
|
A | C | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-6112T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561755 | ||||||
| chr8:144561755
|
ATCCAGTG others(17): Show |
A | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513-6136_513-6113d others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561755 | ||||||
| chr8:144561771
|
C | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-6128G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561771 | ||||||
| chr8:144561796
|
G | A | 17 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(14): Show | 17 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.513-6153C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561796 | ||||||
| chr8:144561796
|
G | GGACTTAC others(17): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-6154_513-6153i others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561796 | ||||||
| chr8:144561796
|
G | GGACTTAC others(17): Show |
13 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.513-6154_513-6153i others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561796 | ||||||
| chr8:144561807
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513-6164G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561807 | ||||||
| chr8:144561835
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-6192G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561835 | ||||||
| chr8:144561838
|
G | A | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-6195C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561838 | ||||||
| chr8:144561855
|
T | C | 49 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.513-6212A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561855 | ||||||
| chr8:144561920
|
A | G | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-6277T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561920 | ||||||
| chr8:144561941
|
C | CACTCCAG others(13): Show |
1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.513-6318_513-6299d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561941 | ||||||
| chr8:144561941
|
CACTCCAG others(13): Show |
C | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513-6318_513-6299d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561941 | ||||||
| chr8:144561964
|
T | C | 7 | a0001c0001t0003g0023a0001c0001t0021g0062a0001c0004t0006g0069others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.513-6321A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561964 | ||||||
| chr8:144561984
|
CCCAGTGG others(13): Show |
C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513-6361_513-6342d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144561984 | ||||||
| chr8:144562021
|
C | CACTCCAG others(17): Show |
3 | a0001c0001t0001g0053a0001c0001t0004g0158a0001c0002t0001g0082 | 3 | HG02135.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.513-6402_513-6379d others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562021 | ||||||
| chr8:144562021
|
CACTCCAG others(17): Show |
C | 47 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0213others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.513-6402_513-6379d others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562021 | ||||||
| chr8:144562021
|
CACTCCAG others(41): Show |
C | 13 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(10): Show | 13 | HG02145.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.513-6426_513-6379d others(50): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562021 | ||||||
| chr8:144562021
|
CACTCCAG others(65): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513-6450_513-6379d others(74): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562021 | ||||||
| chr8:144562183
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.513-6540A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562183 | ||||||
| chr8:144562191
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6548C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562191 | ||||||
| chr8:144562199
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.513-6556G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562199 | ||||||
| chr8:144562200
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6557C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562200 | ||||||
| chr8:144562201
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6558C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562201 | ||||||
| chr8:144562202
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6559C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562202 | ||||||
| chr8:144562203
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6560G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562203 | ||||||
| chr8:144562204
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6561A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562204 | ||||||
| chr8:144562219
|
T | C | 45 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0198others(42): Show | 45 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.513-6576A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562219 | ||||||
| chr8:144562222
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6579T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562222 | ||||||
| chr8:144562244
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6601T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562244 | ||||||
| chr8:144562246
|
ACTCCAGT others(13): Show |
A | 73 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.513-6623_513-6604d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562246 | ||||||
| chr8:144562248
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6605A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562248 | ||||||
| chr8:144562264
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6621C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562264 | ||||||
| chr8:144562265
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6622A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562265 | ||||||
| chr8:144562266
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.513-6623C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562266 | ||||||
| chr8:144562285
|
T | G | 2 | a0001c0001t0001g0033a0001c0007t0017g0019 | 2 | HG03195.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.513-6642A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562285 | ||||||
| chr8:144562288
|
T | TCCAGTGG others(33): Show |
1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6646_513-6645i others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562288 | ||||||
| chr8:144562303
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.513-6660G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562303 | ||||||
| chr8:144562304
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0146 | 2 | NA19012.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.513-6661C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562304 | ||||||
| chr8:144562305
|
G | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0146a0001c0007t0017g0019 | 3 | HG03195.hp2 NA19012.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.513-6662C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562305 | ||||||
| chr8:144562305
|
GGCTCCAG others(13): Show |
G | 1 | a0001c0002t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.513-6682_513-6663d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562305 | ||||||
| chr8:144562324
|
A | ACGCTCCA others(33): Show |
1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-6682_513-6681i others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562324 | ||||||
| chr8:144562324
|
A | G | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6681T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562324 | ||||||
| chr8:144562325
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.513-6682G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562325 | ||||||
| chr8:144562331
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.513-6688T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562331 | ||||||
| chr8:144562344
|
A | G | 4 | a0001c0001t0001g0146a0001c0007t0003g0078a0001c0007t0017g0019others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.513-6701T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562344 | ||||||
| chr8:144562345
|
C | G | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6702G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562345 | ||||||
| chr8:144562346
|
G | A | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6703C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562346 | ||||||
| chr8:144562348
|
T | C | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6705A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562348 | ||||||
| chr8:144562348
|
TCCAGTGG others(13): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.513-6725_513-6706d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562348 | ||||||
| chr8:144562349
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6706G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562349 | ||||||
| chr8:144562365
|
G | C | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6722C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562365 | ||||||
| chr8:144562366
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-6723T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562366 | ||||||
| chr8:144562368
|
C | T | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6725G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562368 | ||||||
| chr8:144562369
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-6726G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562369 | ||||||
| chr8:144562383
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-6740G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562383 | ||||||
| chr8:144562386
|
G | A | 3 | a0001c0002t0001g0020a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6743C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562386 | ||||||
| chr8:144562404
|
G | GGACCTCA others(85): Show |
1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-6762_513-6761i others(94): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562404 | ||||||
| chr8:144562406
|
G | A | 3 | a0001c0007t0003g0078a0001c0007t0017g0019a0005c0013t0002g0195 | 3 | HG02257.hp1 HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6763C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562406 | ||||||
| chr8:144562408
|
TCCAGTGG others(13): Show |
T | 1 | a0001c0002t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.513-6785_513-6766d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562408 | ||||||
| chr8:144562425
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.513-6782C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562425 | ||||||
| chr8:144562425
|
G | GACTCACT others(105): Show |
1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-6783_513-6782i others(114): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562425 | ||||||
| chr8:144562426
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.513-6783T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562426 | ||||||
| chr8:144562428
|
C | T | 3 | a0001c0001t0001g0146a0001c0007t0003g0078a0001c0007t0017g0019 | 3 | HG02257.hp1 HG03195.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.513-6785G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562428 | ||||||
| chr8:144562429
|
C | T | 41 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(38): Show | 41 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.513-6786G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562429 | ||||||
| chr8:144562444
|
G | A | 2 | a0001c0001t0001g0016a0003c0011t0001g0072 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.513-6801C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562444 | ||||||
| chr8:144562445
|
G | C | 41 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(38): Show | 41 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.513-6802C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562445 | ||||||
| chr8:144562445
|
G | GACTCCAG others(13): Show |
1 | a0001c0001t0011g0046 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.513-6822_513-6803d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562445 | ||||||
| chr8:144562448
|
T | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-6805A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562448 | ||||||
| chr8:144562454
|
G | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-6811C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562454 | ||||||
| chr8:144562464
|
G | A | 2 | a0001c0007t0003g0078a0005c0013t0002g0195 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.513-6821C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562464 | ||||||
| chr8:144562465
|
C | G | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6822G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562465 | ||||||
| chr8:144562468
|
T | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6825A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562468 | ||||||
| chr8:144562474
|
G | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6831C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562474 | ||||||
| chr8:144562484
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6841C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562484 | ||||||
| chr8:144562484
|
G | GGACT | 47 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.513-6842_513-6841i others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562484 | ||||||
| chr8:144562485
|
C | G | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-6842G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562485 | ||||||
| chr8:144562509
|
C | CACTCCAG others(33): Show |
1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-6867_513-6866i others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562509
|
C | CACTCCAG others(77): Show |
1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-6867_513-6866i others(86): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562509
|
C | CACTCCAG others(185): Show |
2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-6867_513-6866i others(194): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562509
|
C | CACTCCAG others(161): Show |
1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513-6867_513-6866i others(170): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562509
|
C | CACTCCAG others(157): Show |
17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-6867_513-6866i others(166): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562509
|
C | CACTCCAG others(181): Show |
10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-6867_513-6866i others(190): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562509 | ||||||
| chr8:144562512
|
T | C | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-6869A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562512 | ||||||
| chr8:144562529
|
G | GACTCCAG others(13): Show |
3 | a0001c0007t0003g0078a0001c0007t0017g0019a0005c0013t0002g0195 | 3 | HG02257.hp1 HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.513-6906_513-6887d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562529 | ||||||
| chr8:144562529
|
G | GACTCCAG others(205): Show |
9 | a0001c0003t0001g0005a0001c0003t0001g0110a0001c0003t0009g0004others(6): Show | 9 | HG00408.hp2 HG00639.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.513-6887_513-6886i others(214): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562529 | ||||||
| chr8:144562529
|
G | GACTCCAG others(225): Show |
1 | a0001c0003t0001g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513-6887_513-6886i others(234): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562529 | ||||||
| chr8:144562548
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6905T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562548 | ||||||
| chr8:144562549
|
C | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6906G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562549 | ||||||
| chr8:144562567
|
CACACTCC others(13): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.513-6944_513-6925d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562567 | ||||||
| chr8:144562568
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6925T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562568 | ||||||
| chr8:144562569
|
C | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6926G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562569 | ||||||
| chr8:144562572
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6929A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562572 | ||||||
| chr8:144562578
|
G | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6935C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562578 | ||||||
| chr8:144562587
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6944A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562587 | ||||||
| chr8:144562636
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-6993G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562636 | ||||||
| chr8:144562646
|
A | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7003T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562646 | ||||||
| chr8:144562652
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7009C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562652 | ||||||
| chr8:144562653
|
G | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7010C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562653 | ||||||
| chr8:144562677
|
C | CCAGTGGT others(109): Show |
1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7035_513-7034i others(118): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562677 | ||||||
| chr8:144562680
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7037A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562680 | ||||||
| chr8:144562690
|
T | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7047A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562690 | ||||||
| chr8:144562741
|
C | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7098G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562741 | ||||||
| chr8:144562744
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7101G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562744 | ||||||
| chr8:144562744
|
CCCAGTGG others(13): Show |
C | 7 | a0001c0001t0021g0062a0001c0002t0019g0125a0001c0004t0006g0069others(4): Show | 7 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.513-7121_513-7102d others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562744 | ||||||
| chr8:144562759
|
T | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.513-7116A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562759 | ||||||
| chr8:144562764
|
T | TCACTCCA others(17): Show |
1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-7122_513-7121i others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562764 | ||||||
| chr8:144562788
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.513-7145A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144562788 | ||||||
| chr8:144563194
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.513-7551A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563194 | ||||||
| chr8:144563229
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.513-7586T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563229 | ||||||
| chr8:144563348
|
G | C | 12 | a0001c0001t0002g0131a0001c0001t0007g0168a0001c0002t0001g0020others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.513-7705C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563348 | ||||||
| chr8:144563523
|
A | G | 2 | a0001c0001t0001g0229a0001c0002t0001g0162 | 2 | HG02109.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.513-7880T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563523 | ||||||
| chr8:144563534
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.513-7891G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563534 | ||||||
| chr8:144563780
|
C | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.513-8137G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563780 | ||||||
| chr8:144563789
|
T | TA | 35 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(32): Show | 35 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.513-8147dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563789 | ||||||
| chr8:144563907
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513-8264G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144563907 | ||||||
| chr8:144564303
|
G | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.513-8660C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564303 | ||||||
| chr8:144564333
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-8690G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564333 | ||||||
| chr8:144564371
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.513-8728T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564371 | ||||||
| chr8:144564482
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.513-8839T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564482 | ||||||
| chr8:144564622
|
C | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0002t0001g0020others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-8979G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564622 | ||||||
| chr8:144564810
|
T | TA | 18 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(15): Show | 18 | HG01175.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.513-9168dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564810 | ||||||
| chr8:144564854
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.513-9211G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564854 | ||||||
| chr8:144564969
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.513-9326C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564969 | ||||||
| chr8:144564974
|
G | C | 1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.513-9331C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144564974 | ||||||
| chr8:144565024
|
C | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-9381G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565024 | ||||||
| chr8:144565140
|
T | C | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.513-9497A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565140 | ||||||
| chr8:144565179
|
G | A | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-9536C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565179 | ||||||
| chr8:144565259
|
C | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(15): Show | 18 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.513-9616G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565259 | ||||||
| chr8:144565316
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.513-9673G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565316 | ||||||
| chr8:144565460
|
G | A | 17 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0002g0131others(14): Show | 17 | HG00323.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.513-9817C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565460 | ||||||
| chr8:144565510
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.513-9867C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565510 | ||||||
| chr8:144565551
|
C | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-9908G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565551 | ||||||
| chr8:144565569
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.513-9926C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565569 | ||||||
| chr8:144565716
|
T | C | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.513-10073A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565716 | ||||||
| chr8:144565757
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.513-10114G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565757 | ||||||
| chr8:144565791
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0002t0001g0159 | 3 | HG02451.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.513-10148C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565791 | ||||||
| chr8:144565902
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-10259C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565902 | ||||||
| chr8:144565928
|
C | CA | 32 | a0001c0001t0001g0024a0001c0001t0001g0144a0001c0001t0001g0151others(29): Show | 32 | HG01952.hp1 HG01975.hp2 HG01981.hp2 others(29): Show |
intron_variant | MODIFIER | c.513-10286dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565928 | ||||||
| chr8:144565957
|
A | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(29): Show | 32 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.513-10314T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565957 | ||||||
| chr8:144565980
|
G | C | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.513-10337C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144565980 | ||||||
| chr8:144566013
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513-10370C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566013 | ||||||
| chr8:144566032
|
C | T | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.513-10389G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566032 | ||||||
| chr8:144566086
|
CCT | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(16): Show | 19 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.513-10445_513-1044 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566086 | ||||||
| chr8:144566099
|
C | A | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.513-10456G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566099 | ||||||
| chr8:144566445
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.513-10802A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566445 | ||||||
| chr8:144566576
|
C | T | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.513-10933G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566576 | ||||||
| chr8:144566593
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.513-10950A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566593 | ||||||
| chr8:144566653
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.513-11010G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566653 | ||||||
| chr8:144566816
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513-11173G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566816 | ||||||
| chr8:144566862
|
GA | G | 27 | a0001c0001t0001g0050a0001c0001t0001g0223a0001c0001t0001g0224others(24): Show | 27 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.513-11220delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566862 | ||||||
| chr8:144566862
|
GAA | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-11221_513-1122 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566862 | ||||||
| chr8:144566880
|
A | C | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-11237T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144566880 | ||||||
| chr8:144567171
|
T | C | 2 | a0001c0001t0001g0016a0003c0011t0001g0072 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.513-11528A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567171 | ||||||
| chr8:144567242
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.513-11599A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567242 | ||||||
| chr8:144567388
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513-11745G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567388 | ||||||
| chr8:144567432
|
T | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513-11789A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567432 | ||||||
| chr8:144567432
|
T | G | 30 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(27): Show | 30 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.513-11789A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567432 | ||||||
| chr8:144567441
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-11798G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567441 | ||||||
| chr8:144567557
|
C | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(19): Show | 22 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.513-11914G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567557 | ||||||
| chr8:144567582
|
A | G | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.513-11939T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567582 | ||||||
| chr8:144567594
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(19): Show | 22 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.513-11951T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567594 | ||||||
| chr8:144567718
|
T | C | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-12075A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567718 | ||||||
| chr8:144567722
|
C | T | 20 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(17): Show | 20 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.513-12079G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567722 | ||||||
| chr8:144567739
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-12096C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567739 | ||||||
| chr8:144567827
|
T | C | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.513-12184A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567827 | ||||||
| chr8:144567976
|
ATC | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0144a0001c0002t0001g0035 | 3 | HG01981.hp2 HG02080.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.513-12335_513-1233 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144567976 | ||||||
| chr8:144568011
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.513-12368C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568011 | ||||||
| chr8:144568020
|
C | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513-12377G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568020 | ||||||
| chr8:144568070
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.513-12427C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568070 | ||||||
| chr8:144568211
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.513-12568C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568211 | ||||||
| chr8:144568261
|
C | G | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.512+12585G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568261 | ||||||
| chr8:144568317
|
G | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0241 | 2 | HG01975.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.512+12529C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568317 | ||||||
| chr8:144568333
|
C | CA | 107 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0030others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.512+12512dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568333 | ||||||
| chr8:144568333
|
C | CAA | 65 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0033others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.512+12511_512+1251 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568333 | ||||||
| chr8:144568333
|
C | CAAA | 7 | a0001c0001t0001g0175a0001c0001t0001g0190a0001c0001t0001g0198others(4): Show | 7 | HG01175.hp2 HG01891.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+12510_512+1251 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568333 | ||||||
| chr8:144568333
|
CA | C | 6 | a0001c0001t0001g0231a0001c0001t0004g0237a0001c0001t0007g0239others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+12512delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568333 | ||||||
| chr8:144568678
|
A | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+12168T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568678 | ||||||
| chr8:144568825
|
A | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+12021T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568825 | ||||||
| chr8:144568829
|
G | A | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+12017C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568829 | ||||||
| chr8:144568873
|
GA | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+11972delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568873 | ||||||
| chr8:144568885
|
A | T | 29 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(26): Show | 29 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.512+11961T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568885 | ||||||
| chr8:144568944
|
C | T | 1 | a0001c0003t0009g0004 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.512+11902G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568944 | ||||||
| chr8:144568962
|
G | A | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.512+11884C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568962 | ||||||
| chr8:144568966
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.512+11880A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568966 | ||||||
| chr8:144568970
|
A | C | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.512+11876T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568970 | ||||||
| chr8:144568981
|
T | G | 30 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(27): Show | 30 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.512+11865A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144568981 | ||||||
| chr8:144569018
|
A | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+11828T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569018 | ||||||
| chr8:144569280
|
G | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0175a0001c0001t0001g0176others(3): Show | 6 | HG01099.hp2 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+11566C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569280 | ||||||
| chr8:144569405
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.512+11441G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569405 | ||||||
| chr8:144569697
|
A | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+11149T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569697 | ||||||
| chr8:144569810
|
C | A | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.512+11036G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569810 | ||||||
| chr8:144569810
|
C | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+11036G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144569810 | ||||||
| chr8:144570082
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.512+10764C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570082 | ||||||
| chr8:144570140
|
C | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+10706G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570140 | ||||||
| chr8:144570141
|
A | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.512+10705T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570141 | ||||||
| chr8:144570175
|
G | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+10671C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570175 | ||||||
| chr8:144570232
|
A | G | 1 | a0001c0003t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.512+10614T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570232 | ||||||
| chr8:144570235
|
C | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.512+10611G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570235 | ||||||
| chr8:144570318
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.512+10528C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570318 | ||||||
| chr8:144570454
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512+10392T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570454 | ||||||
| chr8:144570521
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.512+10325G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570521 | ||||||
| chr8:144570889
|
T | G | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+9957A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144570889 | ||||||
| chr8:144571024
|
C | T | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.512+9822G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571024 | ||||||
| chr8:144571051
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.512+9795C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571051 | ||||||
| chr8:144571073
|
G | T | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+9773C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571073 | ||||||
| chr8:144571160
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+9686C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571160 | ||||||
| chr8:144571217
|
C | T | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.512+9629G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571217 | ||||||
| chr8:144571872
|
C | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+8974G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144571872 | ||||||
| chr8:144572227
|
T | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+8619A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572227 | ||||||
| chr8:144572255
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0197 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+8591G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572255 | ||||||
| chr8:144572325
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.512+8521G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572325 | ||||||
| chr8:144572342
|
C | T | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+8504G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572342 | ||||||
| chr8:144572420
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.512+8426G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572420 | ||||||
| chr8:144572467
|
A | C | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+8379T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572467 | ||||||
| chr8:144572966
|
A | G | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.512+7880T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572966 | ||||||
| chr8:144572999
|
T | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+7847A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144572999 | ||||||
| chr8:144573343
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.512+7503T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144573343 | ||||||
| chr8:144573497
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+7349G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144573497 | ||||||
| chr8:144573645
|
T | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.512+7201A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144573645 | ||||||
| chr8:144573797
|
T | C | 1 | a0001c0001t0005g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.512+7049A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144573797 | ||||||
| chr8:144573939
|
G | A | 1 | a0001c0001t0004g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.512+6907C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144573939 | ||||||
| chr8:144574025
|
C | T | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+6821G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574025 | ||||||
| chr8:144574034
|
A | G | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.512+6812T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574034 | ||||||
| chr8:144574066
|
A | G | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+6780T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574066 | ||||||
| chr8:144574081
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.512+6765C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574081 | ||||||
| chr8:144574091
|
T | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.512+6755A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574091 | ||||||
| chr8:144574149
|
G | GA | 39 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(36): Show | 39 | HG01192.hp2 HG02145.hp1 HG02145.hp2 others(36): Show |
intron_variant | MODIFIER | c.512+6696dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574149 | ||||||
| chr8:144574149
|
G | GAA | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.512+6695_512+6696d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574149 | ||||||
| chr8:144574149
|
GA | G | 68 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0047others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.512+6696delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574149 | ||||||
| chr8:144574181
|
A | AGACGAG | 25 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(22): Show | 25 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.512+6664_512+6665i others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574181 | ||||||
| chr8:144574181
|
A | AGACGAGG others(2): Show |
13 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.512+6664_512+6665i others(11): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574181 | ||||||
| chr8:144574181
|
A | AGACGAGG others(5): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.512+6664_512+6665i others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574181 | ||||||
| chr8:144574184
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0004g0237a0001c0002t0001g0025 | 3 | HG02976.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.512+6662A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574184 | ||||||
| chr8:144574184
|
T | G | 40 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(37): Show | 40 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.512+6662A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574184 | ||||||
| chr8:144574392
|
T | C | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.512+6454A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574392 | ||||||
| chr8:144574396
|
T | C | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.512+6450A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574396 | ||||||
| chr8:144574398
|
T | C | 55 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.512+6448A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574398 | ||||||
| chr8:144574408
|
T | C | 4 | a0001c0002t0001g0106a0001c0002t0001g0111a0001c0002t0001g0112others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+6438A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574408 | ||||||
| chr8:144574446
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.512+6400T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574446 | ||||||
| chr8:144574452
|
C | A | 1 | a0001c0004t0006g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.512+6394G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574452 | ||||||
| chr8:144574453
|
C | G | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.512+6393G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574453 | ||||||
| chr8:144574461
|
C | G | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.512+6385G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574461 | ||||||
| chr8:144574543
|
G | A | 29 | a0001c0001t0001g0151a0001c0001t0001g0223a0001c0001t0001g0224others(26): Show | 29 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.512+6303C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574543 | ||||||
| chr8:144574587
|
T | C | 1 | a0001c0002t0019g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.512+6259A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574587 | ||||||
| chr8:144574620
|
G | A | 45 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(42): Show | 45 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.512+6226C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574620 | ||||||
| chr8:144574631
|
G | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+6215C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574631 | ||||||
| chr8:144574669
|
G | A | 2 | a0001c0001t0012g0040a0001c0007t0017g0019 | 2 | HG03195.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.512+6177C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574669 | ||||||
| chr8:144574710
|
T | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.512+6136A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574710 | ||||||
| chr8:144574714
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0002g0123 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.512+6132A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574714 | ||||||
| chr8:144574717
|
G | A | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+6129C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574717 | ||||||
| chr8:144574769
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0012g0040a0001c0001t0014g0054others(1): Show | 4 | HG00438.hp1 NA18990.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+6077A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144574769 | ||||||
| chr8:144575044
|
C | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+5802G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575044 | ||||||
| chr8:144575049
|
G | A | 42 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(39): Show | 42 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.512+5797C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575049 | ||||||
| chr8:144575118
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.512+5728A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575118 | ||||||
| chr8:144575148
|
T | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+5698A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575148 | ||||||
| chr8:144575149
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+5697C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575149 | ||||||
| chr8:144575186
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+5660A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575186 | ||||||
| chr8:144575190
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+5656G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575190 | ||||||
| chr8:144575345
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.512+5501C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575345 | ||||||
| chr8:144575492
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.512+5354C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575492 | ||||||
| chr8:144575494
|
CACAA | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+5348_512+5351d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575494 | ||||||
| chr8:144575804
|
T | C | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.512+5042A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575804 | ||||||
| chr8:144575857
|
G | A | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.512+4989C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575857 | ||||||
| chr8:144575873
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.512+4973T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144575873 | ||||||
| chr8:144576202
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.512+4644C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576202 | ||||||
| chr8:144576315
|
AGAGT | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.512+4527_512+4530d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576315 | ||||||
| chr8:144576332
|
C | CA | 16 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0002g0241others(13): Show | 16 | HG00741.hp1 HG01496.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+4513dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576332 | ||||||
| chr8:144576332
|
CA | C | 70 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0034others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.512+4513delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576332 | ||||||
| chr8:144576332
|
CAA | C | 22 | a0001c0001t0001g0016a0001c0001t0003g0063a0001c0001t0003g0068others(19): Show | 22 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.512+4512_512+4513d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576332 | ||||||
| chr8:144576332
|
CAAA | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0003g0023others(9): Show | 12 | HG02572.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.512+4511_512+4513d others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576332 | ||||||
| chr8:144576332
|
CAAAA | C | 8 | a0001c0001t0001g0228a0001c0001t0004g0152a0001c0001t0004g0237others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.512+4510_512+4513d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576332 | ||||||
| chr8:144576404
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.512+4442G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576404 | ||||||
| chr8:144576545
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.512+4301G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576545 | ||||||
| chr8:144576624
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512+4222G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576624 | ||||||
| chr8:144576654
|
A | G | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.512+4192T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576654 | ||||||
| chr8:144576720
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.512+4126C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576720 | ||||||
| chr8:144576742
|
C | T | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+4104G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576742 | ||||||
| chr8:144576772
|
G | C | 1 | a0001c0004t0006g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.512+4074C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576772 | ||||||
| chr8:144576810
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512+4036G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576810 | ||||||
| chr8:144576880
|
G | A | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+3966C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576880 | ||||||
| chr8:144576891
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512+3955C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144576891 | ||||||
| chr8:144577063
|
T | G | 72 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(69): Show | 72 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.512+3783A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577063 | ||||||
| chr8:144577085
|
C | T | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+3761G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577085 | ||||||
| chr8:144577195
|
T | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.512+3651A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577195 | ||||||
| chr8:144577199
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.512+3647T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577199 | ||||||
| chr8:144577390
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.512+3456T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577390 | ||||||
| chr8:144577536
|
T | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+3310A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577536 | ||||||
| chr8:144577604
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+3242C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577604 | ||||||
| chr8:144577648
|
G | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(8): Show | 11 | HG02004.hp1 HG02135.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+3198C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577648 | ||||||
| chr8:144577688
|
T | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+3158A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577688 | ||||||
| chr8:144577725
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.512+3121G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577725 | ||||||
| chr8:144577964
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0100 | 2 | NA18945.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.512+2882T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144577964 | ||||||
| chr8:144578006
|
A | G | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.512+2840T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578006 | ||||||
| chr8:144578166
|
G | C | 42 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(39): Show | 42 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.512+2680C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578166 | ||||||
| chr8:144578240
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.512+2606A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578240 | ||||||
| chr8:144578315
|
A | G | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.512+2531T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578315 | ||||||
| chr8:144578437
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.512+2409G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578437 | ||||||
| chr8:144578729
|
C | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.512+2117G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578729 | ||||||
| chr8:144578774
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.512+2072C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578774 | ||||||
| chr8:144578946
|
T | C | 43 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+1900A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144578946 | ||||||
| chr8:144579126
|
C | T | 30 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(27): Show | 30 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(27): Show |
intron_variant | MODIFIER | c.512+1720G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579126 | ||||||
| chr8:144579158
|
T | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0146 | 2 | NA19082.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.512+1688A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579158 | ||||||
| chr8:144579201
|
C | CA | 31 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0141others(28): Show | 31 | HG00609.hp2 HG01168.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.512+1644dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579201
|
C | CAA | 13 | a0001c0001t0001g0016a0001c0001t0001g0210a0001c0001t0020g0079others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.512+1643_512+1644d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579201
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0226others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1637_512+1644d others(10): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579201
|
CA | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0177a0001c0001t0001g0236others(5): Show | 8 | HG00323.hp1 HG00558.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+1644delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579201
|
CAAAA | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.512+1641_512+1644d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579201
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512+1633_512+1644d others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579201 | ||||||
| chr8:144579455
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.512+1391G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579455 | ||||||
| chr8:144579630
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.512+1216A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579630 | ||||||
| chr8:144579662
|
C | G | 42 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(39): Show | 42 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.512+1184G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579662 | ||||||
| chr8:144579751
|
C | G | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.512+1095G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579751 | ||||||
| chr8:144579817
|
G | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.512+1029C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579817 | ||||||
| chr8:144579984
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.512+862G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579984 | ||||||
| chr8:144579996
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.512+850T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144579996 | ||||||
| chr8:144580009
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.512+837G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580009 | ||||||
| chr8:144580118
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.512+728G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580118 | ||||||
| chr8:144580151
|
C | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.512+695G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580151 | ||||||
| chr8:144580304
|
G | A | 2 | a0002c0008t0001g0067a0002c0008t0001g0142 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.512+542C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580304 | ||||||
| chr8:144580527
|
G | A | 2 | a0001c0001t0020g0079a0001c0017t0001g0064 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.512+319C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580527 | ||||||
| chr8:144580577
|
C | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0047others(1): Show | 4 | NA18945.hp1 NA18999.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.512+269G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580577 | ||||||
| chr8:144580577
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.512+269G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580577 | ||||||
| chr8:144580647
|
T | A | 11 | a0001c0001t0002g0134a0001c0001t0002g0138a0001c0001t0002g0139others(8): Show | 11 | HG01975.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.512+199A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580647 | ||||||
| chr8:144580770
|
AC | A | 34 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(31): Show | 34 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(31): Show |
intron_variant | MODIFIER | c.512+75delG | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | 144580770 | ||||||
| chr8:144581297
|
A | G | 244 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.81-20T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581297 | ||||||
| chr8:144581389
|
T | C | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.81-112A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581389 | ||||||
| chr8:144581391
|
G | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-114C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581391 | ||||||
| chr8:144581404
|
C | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-127G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581404 | ||||||
| chr8:144581475
|
C | T | 2 | a0001c0007t0017g0019a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81-198G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581475 | ||||||
| chr8:144581583
|
T | C | 217 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.81-306A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581583 | ||||||
| chr8:144581600
|
G | A | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.81-323C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581600 | ||||||
| chr8:144581695
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-418G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581695 | ||||||
| chr8:144581709
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81-432C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581709 | ||||||
| chr8:144581733
|
T | C | 3 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0089 | 3 | HG02683.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.81-456A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581733 | ||||||
| chr8:144581876
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.81-599C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581876 | ||||||
| chr8:144581910
|
A | G | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.81-633T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581910 | ||||||
| chr8:144581983
|
TC | T | 15 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(12): Show | 15 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.81-707delG | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581983 | ||||||
| chr8:144581994
|
A | ACCCTGCG others(47): Show |
1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-771_81-718dupCT others(52): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581994 | ||||||
| chr8:144581994
|
ACCCTGCG others(47): Show |
A | 1 | a0001c0001t0001g0204 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81-771_81-718delCT others(52): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144581994 | ||||||
| chr8:144582191
|
G | A | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-914C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582191 | ||||||
| chr8:144582212
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-935C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582212 | ||||||
| chr8:144582253
|
C | T | 1 | a0001c0006t0001g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.81-976G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582253 | ||||||
| chr8:144582603
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-1326C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582603 | ||||||
| chr8:144582651
|
C | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(64): Show | 67 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.81-1374G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582651 | ||||||
| chr8:144582666
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.81-1389C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582666 | ||||||
| chr8:144582699
|
G | T | 5 | a0001c0005t0001g0006a0001c0005t0001g0010a0001c0005t0001g0011others(2): Show | 5 | HG00639.hp1 HG01168.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-1422C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582699 | ||||||
| chr8:144582714
|
C | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81-1437G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582714 | ||||||
| chr8:144582841
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.81-1564G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582841 | ||||||
| chr8:144582963
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.81-1686C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144582963 | ||||||
| chr8:144583025
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-1748C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583025 | ||||||
| chr8:144583083
|
C | T | 6 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0005g0187others(3): Show | 6 | HG00323.hp2 HG00735.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-1806G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583083 | ||||||
| chr8:144583093
|
G | C | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-1816C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583093 | ||||||
| chr8:144583172
|
G | T | 1 | a0001c0001t0001g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.81-1895C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583172 | ||||||
| chr8:144583469
|
G | T | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81-2192C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583469 | ||||||
| chr8:144583522
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-2245C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583522 | ||||||
| chr8:144583531
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81-2254C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583531 | ||||||
| chr8:144583573
|
C | T | 16 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(13): Show | 16 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.81-2296G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583573 | ||||||
| chr8:144583598
|
T | C | 49 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.81-2321A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583598 | ||||||
| chr8:144583680
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-2403G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583680 | ||||||
| chr8:144583737
|
G | A | 11 | a0001c0001t0002g0134a0001c0001t0002g0138a0001c0001t0002g0139others(8): Show | 11 | HG01975.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-2460C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583737 | ||||||
| chr8:144583807
|
A | C | 3 | a0001c0001t0001g0024a0001c0002t0001g0025a0001c0007t0017g0019 | 3 | HG03041.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.81-2530T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583807 | ||||||
| chr8:144583892
|
T | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-2615A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144583892 | ||||||
| chr8:144584054
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81-2777T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584054 | ||||||
| chr8:144584400
|
A | C | 33 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(30): Show | 33 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(30): Show |
intron_variant | MODIFIER | c.81-3123T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584400 | ||||||
| chr8:144584588
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-3311G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584588 | ||||||
| chr8:144584625
|
T | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81-3348A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584625 | ||||||
| chr8:144584632
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.81-3355C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584632 | ||||||
| chr8:144584671
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.81-3394C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584671 | ||||||
| chr8:144584846
|
G | GTC | 49 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.81-3571_81-3570dup others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584846 | ||||||
| chr8:144584991
|
G | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-3714C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144584991 | ||||||
| chr8:144585124
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.81-3847C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585124 | ||||||
| chr8:144585154
|
A | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-3877T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585154 | ||||||
| chr8:144585161
|
T | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.81-3884A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585161 | ||||||
| chr8:144585212
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81-3935G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585212 | ||||||
| chr8:144585293
|
A | G | 2 | a0001c0001t0003g0023a0001c0001t0021g0062 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.81-4016T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585293 | ||||||
| chr8:144585390
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-4113C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585390 | ||||||
| chr8:144585422
|
G | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81-4145C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585422 | ||||||
| chr8:144585582
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-4305C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585582 | ||||||
| chr8:144585654
|
C | G | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.81-4377G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585654 | ||||||
| chr8:144585670
|
A | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-4393T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585670 | ||||||
| chr8:144585832
|
A | G | 1 | a0001c0002t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81-4555T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585832 | ||||||
| chr8:144585858
|
C | G | 32 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(29): Show | 32 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(29): Show |
intron_variant | MODIFIER | c.81-4581G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585858 | ||||||
| chr8:144585900
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-4623C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144585900 | ||||||
| chr8:144586067
|
C | G | 2 | a0001c0001t0018g0022a0001c0002t0019g0125 | 2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.81-4790G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586067 | ||||||
| chr8:144586413
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-5136C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586413 | ||||||
| chr8:144586666
|
C | T | 48 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(45): Show | 48 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.81-5389G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586666 | ||||||
| chr8:144586677
|
C | T | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-5400G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586677 | ||||||
| chr8:144586714
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.81-5437C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586714 | ||||||
| chr8:144586754
|
C | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-5477G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586754 | ||||||
| chr8:144586825
|
A | G | 32 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(29): Show | 32 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.81-5548T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586825 | ||||||
| chr8:144586942
|
G | A | 1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.81-5665C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144586942 | ||||||
| chr8:144587001
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-5724G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587001 | ||||||
| chr8:144587038
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.81-5761T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587038 | ||||||
| chr8:144587141
|
G | C | 27 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.81-5864C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587141 | ||||||
| chr8:144587142
|
C | T | 27 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.81-5865G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587142 | ||||||
| chr8:144587171
|
C | A | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81-5894G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587171 | ||||||
| chr8:144587183
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-5906T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587183 | ||||||
| chr8:144587309
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81-6032T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587309 | ||||||
| chr8:144587386
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.81-6109G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587386 | ||||||
| chr8:144587394
|
T | C | 7 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0004g0237others(4): Show | 7 | HG02109.hp1 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.81-6117A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587394 | ||||||
| chr8:144587518
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-6241C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587518 | ||||||
| chr8:144587518
|
G | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-6241C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587518 | ||||||
| chr8:144587643
|
G | A | 1 | a0001c0002t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81-6366C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587643 | ||||||
| chr8:144587654
|
CT | C | 10 | a0001c0001t0001g0198a0001c0001t0002g0139a0001c0001t0004g0237others(7): Show | 10 | HG01975.hp1 HG02004.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-6378delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587654 | ||||||
| chr8:144587690
|
C | T | 25 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0238others(22): Show | 25 | HG02055.hp2 HG02451.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.81-6413G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587690 | ||||||
| chr8:144587710
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.81-6433C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587710 | ||||||
| chr8:144587715
|
C | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-6438G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587715 | ||||||
| chr8:144587723
|
C | T | 41 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0058others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.81-6446G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587723 | ||||||
| chr8:144587802
|
G | C | 26 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(23): Show | 26 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.81-6525C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587802 | ||||||
| chr8:144587822
|
C | T | 3 | a0001c0001t0007g0018a0001c0001t0021g0062a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.81-6545G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587822 | ||||||
| chr8:144587828
|
T | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.81-6551A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587828 | ||||||
| chr8:144587834
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81-6557C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587834 | ||||||
| chr8:144587890
|
G | A | 14 | a0001c0001t0002g0131a0001c0001t0007g0168a0001c0002t0001g0020others(11): Show | 14 | HG00323.hp1 HG01192.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.81-6613C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587890 | ||||||
| chr8:144587908
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-6631C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587908 | ||||||
| chr8:144587935
|
G | A | 4 | a0001c0002t0001g0007a0001c0002t0001g0095a0001c0002t0001g0096others(1): Show | 4 | HG02027.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-6658C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144587935 | ||||||
| chr8:144588027
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-6750C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588027 | ||||||
| chr8:144588073
|
A | G | 122 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.81-6796T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588073 | ||||||
| chr8:144588143
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81-6866G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588143 | ||||||
| chr8:144588144
|
G | A | 1 | a0001c0005t0001g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81-6867C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588144 | ||||||
| chr8:144588189
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-6912T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588189 | ||||||
| chr8:144588217
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-6940G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588217 | ||||||
| chr8:144588226
|
A | G | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81-6949T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588226 | ||||||
| chr8:144588243
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.81-6966G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588243 | ||||||
| chr8:144588268
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-6991G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588268 | ||||||
| chr8:144588302
|
C | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81-7025G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588302 | ||||||
| chr8:144588319
|
T | C | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.81-7042A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588319 | ||||||
| chr8:144588370
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.81-7093G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588370 | ||||||
| chr8:144588384
|
A | G | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.81-7107T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588384 | ||||||
| chr8:144588523
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-7246C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588523 | ||||||
| chr8:144588646
|
A | G | 24 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(21): Show | 24 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.81-7369T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588646 | ||||||
| chr8:144588704
|
C | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-7427G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588704 | ||||||
| chr8:144588728
|
G | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-7451C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588728 | ||||||
| chr8:144588771
|
T | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-7494A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588771 | ||||||
| chr8:144588780
|
T | G | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-7503A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588780 | ||||||
| chr8:144588975
|
A | G | 13 | a0001c0001t0007g0018a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.81-7698T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144588975 | ||||||
| chr8:144589240
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-7963T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589240 | ||||||
| chr8:144589245
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.81-7968C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589245 | ||||||
| chr8:144589339
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-8062A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589339 | ||||||
| chr8:144589460
|
G | C | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-8183C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589460 | ||||||
| chr8:144589515
|
G | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-8238C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589515 | ||||||
| chr8:144589524
|
G | A | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-8247C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589524 | ||||||
| chr8:144589553
|
T | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.81-8276A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589553 | ||||||
| chr8:144589565
|
A | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-8288T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589565 | ||||||
| chr8:144589678
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-8401C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589678 | ||||||
| chr8:144589681
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.81-8404C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589681 | ||||||
| chr8:144589722
|
G | T | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-8445C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589722 | ||||||
| chr8:144589742
|
A | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-8465T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589742 | ||||||
| chr8:144589842
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81-8565C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589842 | ||||||
| chr8:144589856
|
C | G | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.81-8579G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144589856 | ||||||
| chr8:144590075
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81-8798G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590075 | ||||||
| chr8:144590166
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.81-8889C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590166 | ||||||
| chr8:144590173
|
C | T | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81-8896G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590173 | ||||||
| chr8:144590174
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81-8897C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590174 | ||||||
| chr8:144590207
|
T | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.81-8930A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590207 | ||||||
| chr8:144590305
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81-9028C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590305 | ||||||
| chr8:144590583
|
C | T | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-9306G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590583 | ||||||
| chr8:144590605
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81-9328G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590605 | ||||||
| chr8:144590646
|
G | T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81-9369C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590646 | ||||||
| chr8:144590719
|
A | G | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.81-9442T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590719 | ||||||
| chr8:144590750
|
AC | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.81-9474delG | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144590750 | ||||||
| chr8:144591098
|
C | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.81-9821G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591098 | ||||||
| chr8:144591184
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-9907C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591184 | ||||||
| chr8:144591210
|
G | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-9933C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591210 | ||||||
| chr8:144591366
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.81-10089C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591366 | ||||||
| chr8:144591445
|
C | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-10168G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591445 | ||||||
| chr8:144591514
|
A | G | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81-10237T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591514 | ||||||
| chr8:144591570
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-10293C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591570 | ||||||
| chr8:144591760
|
T | A | 1 | a0001c0001t0001g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81-10483A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591760 | ||||||
| chr8:144591860
|
C | T | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81-10583G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591860 | ||||||
| chr8:144591864
|
G | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81-10587C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591864 | ||||||
| chr8:144591907
|
T | A | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-10630A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591907 | ||||||
| chr8:144591976
|
G | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.81-10699C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144591976 | ||||||
| chr8:144592032
|
A | C | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81-10755T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592032 | ||||||
| chr8:144592143
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-10866T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592143 | ||||||
| chr8:144592243
|
TTGAGCCC others(42): Show |
T | 16 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(13): Show | 16 | HG02027.hp1 HG02055.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.81-11015_81-10967d others(51): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592243 | ||||||
| chr8:144592360
|
A | G | 1 | a0001c0010t0001g0009 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.81-11083T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592360 | ||||||
| chr8:144592371
|
C | CACCTCCT others(187): Show |
2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.81-11288_81-11095d others(196): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592371 | ||||||
| chr8:144592439
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81-11162G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592439 | ||||||
| chr8:144592454
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.81-11177G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592454 | ||||||
| chr8:144592455
|
GGGAAACC others(41): Show |
G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-11226_81-11179d others(50): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592455 | ||||||
| chr8:144592457
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0002g0241 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.81-11180C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592457 | ||||||
| chr8:144592458
|
A | G | 4 | a0001c0002t0001g0007a0001c0002t0001g0095a0001c0002t0001g0096others(1): Show | 4 | HG02027.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-11181T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592458 | ||||||
| chr8:144592502
|
T | TC | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-11226_81-11225i others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592502 | ||||||
| chr8:144592503
|
A | G | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-11226T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592503 | ||||||
| chr8:144592600
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.81-11323C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592600 | ||||||
| chr8:144592845
|
G | A | 1 | a0001c0006t0001g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.81-11568C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592845 | ||||||
| chr8:144592892
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-11615C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592892 | ||||||
| chr8:144592894
|
G | A | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-11617C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144592894 | ||||||
| chr8:144593073
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.81-11796G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593073 | ||||||
| chr8:144593138
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-11861C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593138 | ||||||
| chr8:144593184
|
C | G | 216 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.81-11907G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593184 | ||||||
| chr8:144593234
|
C | T | 3 | a0001c0001t0002g0157a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG02615.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.81-11957G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593234 | ||||||
| chr8:144593297
|
C | T | 57 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.81-12020G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593297 | ||||||
| chr8:144593398
|
A | C | 50 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(47): Show | 50 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.81-12121T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593398 | ||||||
| chr8:144593472
|
A | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+12063T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593472 | ||||||
| chr8:144593535
|
G | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+12000C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593535 | ||||||
| chr8:144593611
|
G | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+11924C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593611 | ||||||
| chr8:144593616
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+11919T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593616 | ||||||
| chr8:144593754
|
C | T | 1 | a0001c0001t0007g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.80+11781G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593754 | ||||||
| chr8:144593806
|
C | T | 3 | a0001c0001t0005g0186a0001c0001t0005g0187a0001c0001t0005g0188 | 3 | HG01168.hp1 HG01169.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80+11729G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593806 | ||||||
| chr8:144593921
|
T | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+11614A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593921 | ||||||
| chr8:144593965
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80+11570G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593965 | ||||||
| chr8:144593981
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+11554G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144593981 | ||||||
| chr8:144594002
|
T | C | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+11533A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594002 | ||||||
| chr8:144594088
|
C | CA | 28 | a0001c0001t0001g0032a0001c0001t0001g0146a0001c0001t0001g0211others(25): Show | 28 | HG00280.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.80+11446dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594088 | ||||||
| chr8:144594088
|
C | CAA | 13 | a0001c0001t0001g0223a0001c0001t0001g0228a0001c0003t0001g0005others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+11445_80+11446d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594088 | ||||||
| chr8:144594088
|
CA | C | 12 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0148others(9): Show | 12 | HG00323.hp1 HG01167.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+11446delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594088 | ||||||
| chr8:144594117
|
C | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+11418G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594117 | ||||||
| chr8:144594415
|
C | T | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.80+11120G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594415 | ||||||
| chr8:144594492
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.80+11043G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594492 | ||||||
| chr8:144594546
|
TAGTC | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+10985_80+10988d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594546 | ||||||
| chr8:144594612
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+10923G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594612 | ||||||
| chr8:144594686
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.80+10849G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594686 | ||||||
| chr8:144594694
|
C | CA | 5 | a0001c0001t0001g0208a0001c0001t0008g0120a0001c0001t0008g0121others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+10840dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594694 | ||||||
| chr8:144594694
|
CA | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0065a0001c0001t0001g0100others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.80+10840delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594694 | ||||||
| chr8:144594694
|
CAA | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+10839_80+10840d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594694 | ||||||
| chr8:144594757
|
CAT | C | 8 | a0001c0001t0007g0018a0001c0004t0006g0069a0001c0004t0006g0070others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+10776_80+10777d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594757 | ||||||
| chr8:144594776
|
T | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+10759A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594776 | ||||||
| chr8:144594809
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+10726G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594809 | ||||||
| chr8:144594875
|
G | T | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80+10660C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144594875 | ||||||
| chr8:144595068
|
T | A | 1 | a0001c0005t0001g0006 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80+10467A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595068 | ||||||
| chr8:144595086
|
A | G | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80+10449T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595086 | ||||||
| chr8:144595128
|
A | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+10407T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595128 | ||||||
| chr8:144595195
|
C | T | 27 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(24): Show | 27 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.80+10340G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595195 | ||||||
| chr8:144595325
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+10210G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595325 | ||||||
| chr8:144595349
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+10186G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595349 | ||||||
| chr8:144595380
|
C | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+10155G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595380 | ||||||
| chr8:144595404
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.80+10131C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595404 | ||||||
| chr8:144595508
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.80+10027A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595508 | ||||||
| chr8:144595598
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0210a0001c0001t0015g0180 | 3 | HG02080.hp2 HG02129.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.80+9937C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595598 | ||||||
| chr8:144595623
|
C | G | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+9912G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595623 | ||||||
| chr8:144595684
|
T | C | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80+9851A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595684 | ||||||
| chr8:144595706
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+9829G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595706 | ||||||
| chr8:144595773
|
C | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+9762G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595773 | ||||||
| chr8:144595917
|
C | T | 18 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(15): Show | 18 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.80+9618G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595917 | ||||||
| chr8:144595964
|
G | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.80+9571C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144595964 | ||||||
| chr8:144596010
|
G | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+9525C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596010 | ||||||
| chr8:144596267
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0015t0001g0101 | 3 | NA18945.hp2 NA18969.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.80+9268C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596267 | ||||||
| chr8:144596271
|
G | GAGGCCTC others(274): Show |
1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+9263_80+9264ins others(281): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596271 | ||||||
| chr8:144596345
|
C | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.80+9190G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596345 | ||||||
| chr8:144596379
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80+9156C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596379 | ||||||
| chr8:144596427
|
A | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+9108T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596427 | ||||||
| chr8:144596543
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.80+8992C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596543 | ||||||
| chr8:144596573
|
T | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+8962A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596573 | ||||||
| chr8:144596659
|
C | T | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80+8876G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596659 | ||||||
| chr8:144596709
|
C | T | 2 | a0001c0002t0001g0015a0005c0013t0002g0195 | 2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.80+8826G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596709 | ||||||
| chr8:144596825
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.80+8710C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144596825 | ||||||
| chr8:144597248
|
C | T | 18 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0002g0131others(15): Show | 18 | HG00323.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80+8287G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597248 | ||||||
| chr8:144597334
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+8201G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597334 | ||||||
| chr8:144597405
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.80+8130G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597405 | ||||||
| chr8:144597487
|
C | T | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.80+8048G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597487 | ||||||
| chr8:144597490
|
A | T | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.80+8045T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597490 | ||||||
| chr8:144597828
|
C | G | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+7707G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597828 | ||||||
| chr8:144597829
|
T | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+7706A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597829 | ||||||
| chr8:144597880
|
A | G | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80+7655T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144597880 | ||||||
| chr8:144598048
|
G | A | 5 | a0001c0002t0001g0003a0001c0006t0001g0171a0001c0006t0001g0181others(2): Show | 5 | HG00099.hp1 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+7487C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598048 | ||||||
| chr8:144598107
|
C | T | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80+7428G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598107 | ||||||
| chr8:144598163
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80+7372G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598163 | ||||||
| chr8:144598191
|
T | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80+7344A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598191 | ||||||
| chr8:144598216
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+7319C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598216 | ||||||
| chr8:144598270
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80+7265C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598270 | ||||||
| chr8:144598334
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+7201C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598334 | ||||||
| chr8:144598515
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+7020G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598515 | ||||||
| chr8:144598516
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80+7019C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598516 | ||||||
| chr8:144598523
|
G | A | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.80+7012C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598523 | ||||||
| chr8:144598878
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+6657C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598878 | ||||||
| chr8:144598939
|
A | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+6596T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144598939 | ||||||
| chr8:144599084
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+6451C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144599084 | ||||||
| chr8:144599352
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+6183C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144599352 | ||||||
| chr8:144599771
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+5764C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144599771 | ||||||
| chr8:144600003
|
G | A | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.80+5532C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600003 | ||||||
| chr8:144600037
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00558.hp1 NA18947.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+5498C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600037 | ||||||
| chr8:144600039
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80+5496C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600039 | ||||||
| chr8:144600097
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.80+5438C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600097 | ||||||
| chr8:144600134
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80+5401G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600134 | ||||||
| chr8:144600174
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80+5361A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600174 | ||||||
| chr8:144600179
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+5356C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600179 | ||||||
| chr8:144600205
|
G | A | 2 | a0001c0001t0001g0031a0001c0002t0022g0217 | 2 | HG02004.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.80+5330C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600205 | ||||||
| chr8:144600214
|
G | T | 6 | a0001c0002t0023g0246a0001c0004t0006g0069a0001c0004t0006g0070others(3): Show | 6 | HG02155.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+5321C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600214 | ||||||
| chr8:144600247
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.80+5288G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600247 | ||||||
| chr8:144600253
|
C | T | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+5282G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600253 | ||||||
| chr8:144600317
|
CGTGTGCA others(77): Show |
C | 1 | a0001c0001t0001g0043 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.80+5134_80+5217del others(84): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600317 | ||||||
| chr8:144600349
|
C | T | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80+5186G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600349 | ||||||
| chr8:144600361
|
C | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+5174G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600361 | ||||||
| chr8:144600362
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(1): Show | 4 | HG01099.hp2 HG01891.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+5173C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600362 | ||||||
| chr8:144600392
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80+5143C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600392 | ||||||
| chr8:144600397
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.80+5138G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600397 | ||||||
| chr8:144600402
|
GTGTGCAC others(37): Show |
G | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+5089_80+5132del others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600402 | ||||||
| chr8:144600423
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80+5112A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600423 | ||||||
| chr8:144600430
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80+5105C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600430 | ||||||
| chr8:144600434
|
G | A | 8 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166others(5): Show | 8 | HG02145.hp1 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+5101C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600434 | ||||||
| chr8:144600440
|
G | A | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.80+5095C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600440 | ||||||
| chr8:144600470
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.80+5065C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600470 | ||||||
| chr8:144600518
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0238 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.80+5017C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600518 | ||||||
| chr8:144600526
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80+5009C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600526 | ||||||
| chr8:144600570
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+4965C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600570 | ||||||
| chr8:144600570
|
G | T | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+4965C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600570 | ||||||
| chr8:144600606
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+4929C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600606 | ||||||
| chr8:144600614
|
G | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+4921C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600614 | ||||||
| chr8:144600633
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+4902G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600633 | ||||||
| chr8:144600653
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.80+4882C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600653 | ||||||
| chr8:144600665
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.80+4870G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600665 | ||||||
| chr8:144600680
|
G | A | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+4855C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600680 | ||||||
| chr8:144600691
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.80+4844G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600691 | ||||||
| chr8:144600730
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.80+4805C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600730 | ||||||
| chr8:144600740
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80+4795G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600740 | ||||||
| chr8:144600745
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.80+4790C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600745 | ||||||
| chr8:144600746
|
T | C | 2 | a0001c0007t0001g0017a0005c0013t0002g0195 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.80+4789A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600746 | ||||||
| chr8:144600781
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+4754C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600781 | ||||||
| chr8:144600787
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80+4748C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600787 | ||||||
| chr8:144600810
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.80+4725G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600810 | ||||||
| chr8:144600811
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+4724C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600811 | ||||||
| chr8:144600812
|
C | T | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+4723G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600812 | ||||||
| chr8:144600818
|
T | G | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80+4717A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600818 | ||||||
| chr8:144600924
|
CTG | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+4609_80+4610del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600924 | ||||||
| chr8:144600946
|
G | C | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+4589C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600946 | ||||||
| chr8:144600975
|
TGGA | T | 8 | a0001c0001t0007g0018a0001c0004t0006g0069a0001c0004t0006g0070others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+4557_80+4559del others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600975 | ||||||
| chr8:144600987
|
T | C | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80+4548A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600987 | ||||||
| chr8:144600989
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4546G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600989 | ||||||
| chr8:144600990
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.80+4545C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600990 | ||||||
| chr8:144600992
|
G | A | 1 | a0001c0007t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.80+4543C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144600992 | ||||||
| chr8:144601002
|
C | CTG | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+4531_80+4532dup others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601002 | ||||||
| chr8:144601046
|
A | G | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+4489T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601046 | ||||||
| chr8:144601083
|
C | T | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4452G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601083 | ||||||
| chr8:144601134
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+4401C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601134 | ||||||
| chr8:144601154
|
CTG | C | 6 | a0001c0002t0001g0007a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | HG01175.hp1 HG02027.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4379_80+4380del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601154 | ||||||
| chr8:144601178
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.80+4357C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601178 | ||||||
| chr8:144601187
|
C | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+4348G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601187 | ||||||
| chr8:144601197
|
T | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+4338A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601197 | ||||||
| chr8:144601207
|
C | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.80+4328G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601207 | ||||||
| chr8:144601213
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.80+4322C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601213 | ||||||
| chr8:144601224
|
A | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+4311T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601224 | ||||||
| chr8:144601235
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+4300G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601235 | ||||||
| chr8:144601236
|
C | CTGTG | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+4295_80+4298dup others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601236 | ||||||
| chr8:144601252
|
G | C | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+4283C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601252 | ||||||
| chr8:144601277
|
T | C | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.80+4258A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601277 | ||||||
| chr8:144601295
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.80+4240G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601295 | ||||||
| chr8:144601296
|
G | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0151others(21): Show | 24 | HG01071.hp1 HG01358.hp1 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.80+4239C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601296 | ||||||
| chr8:144601308
|
CTG | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(9): Show | 12 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+4225_80+4226del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601308 | ||||||
| chr8:144601328
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+4207C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601328 | ||||||
| chr8:144601340
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+4195C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601340 | ||||||
| chr8:144601355
|
T | TGTGCGAG others(67): Show |
1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+4179_80+4180ins others(74): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601355 | ||||||
| chr8:144601389
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80+4146G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601389 | ||||||
| chr8:144601390
|
G | A | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+4145C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601390 | ||||||
| chr8:144601424
|
G | C | 1 | a0001c0001t0008g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.80+4111C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601424 | ||||||
| chr8:144601426
|
G | A | 15 | a0001c0001t0001g0228a0001c0002t0001g0104a0001c0002t0001g0160others(12): Show | 15 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+4109C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601426 | ||||||
| chr8:144601440
|
G | A | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+4095C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601440 | ||||||
| chr8:144601459
|
CGTGGAGG others(49): Show |
C | 1 | a0001c0001t0001g0032 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.80+4020_80+4075del others(56): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601459 | ||||||
| chr8:144601466
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+4069C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601466 | ||||||
| chr8:144601476
|
G | A | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.80+4059C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601476 | ||||||
| chr8:144601488
|
CTG | C | 13 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(10): Show | 13 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.80+4045_80+4046del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601488 | ||||||
| chr8:144601510
|
A | ATGTGTGT others(13): Show |
8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.80+4005_80+4024dup others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601510 | ||||||
| chr8:144601512
|
G | A | 2 | a0001c0002t0001g0140a0001c0002t0001g0222 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80+4023C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601512 | ||||||
| chr8:144601544
|
A | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+3991T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601544 | ||||||
| chr8:144601583
|
TGGA | T | 12 | a0001c0001t0001g0236a0001c0003t0001g0005a0001c0003t0001g0012others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+3949_80+3951del others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601583 | ||||||
| chr8:144601627
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0015g0180 | 3 | HG02109.hp1 HG02129.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.80+3908G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601627 | ||||||
| chr8:144601644
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.80+3891C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601644 | ||||||
| chr8:144601654
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+3881C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601654 | ||||||
| chr8:144601665
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+3870G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601665 | ||||||
| chr8:144601736
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+3799G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601736 | ||||||
| chr8:144601737
|
G | A | 4 | a0001c0002t0001g0088a0001c0002t0009g0028a0002c0008t0001g0067others(1): Show | 4 | HG00558.hp2 HG00639.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+3798C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601737 | ||||||
| chr8:144601745
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.80+3790C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601745 | ||||||
| chr8:144601784
|
CGT | C | 18 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(15): Show | 18 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.80+3749_80+3750del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601784 | ||||||
| chr8:144601788
|
T | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.80+3747A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601788 | ||||||
| chr8:144601801
|
CTG | C | 4 | a0001c0001t0001g0203a0001c0002t0001g0119a0001c0007t0003g0118others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+3732_80+3733del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601801 | ||||||
| chr8:144601810
|
T | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.80+3725A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601810 | ||||||
| chr8:144601843
|
G | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+3692C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601843 | ||||||
| chr8:144601851
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+3684C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601851 | ||||||
| chr8:144601852
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0002g0241 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.80+3683A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601852 | ||||||
| chr8:144601879
|
CTG | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80+3654_80+3655del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601879 | ||||||
| chr8:144601889
|
C | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+3646G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601889 | ||||||
| chr8:144601963
|
T | G | 36 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(33): Show | 36 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.80+3572A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601963 | ||||||
| chr8:144601987
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80+3548C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144601987 | ||||||
| chr8:144602060
|
C | T | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80+3475G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602060 | ||||||
| chr8:144602100
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+3435G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602100 | ||||||
| chr8:144602101
|
G | A | 1 | a0001c0005t0010g0001 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80+3434C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602101 | ||||||
| chr8:144602137
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.80+3398C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602137 | ||||||
| chr8:144602149
|
CTGTG | C | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.80+3382_80+3385del others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602149 | ||||||
| chr8:144602154
|
T | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.80+3381A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602154 | ||||||
| chr8:144602171
|
G | GTGTGTGC others(344): Show |
1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+3363_80+3364ins others(351): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602171 | ||||||
| chr8:144602171
|
GTGTGTGC others(342): Show |
G | 1 | a0001c0002t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80+3015_80+3363del | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602171 | ||||||
| chr8:144602192
|
T | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+3343A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602192 | ||||||
| chr8:144602193
|
G | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+3342C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602193 | ||||||
| chr8:144602219
|
GTGTACCT others(35): Show |
G | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80+3274_80+3315del others(42): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602219 | ||||||
| chr8:144602226
|
T | C | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+3309A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602226 | ||||||
| chr8:144602240
|
TGGA | T | 3 | a0001c0001t0001g0177a0001c0002t0001g0088a0001c0017t0001g0064 | 3 | HG00639.hp2 NA18941.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.80+3292_80+3294del others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602240 | ||||||
| chr8:144602254
|
T | A | 1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.80+3281A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602254 | ||||||
| chr8:144602254
|
T | C | 14 | a0001c0001t0001g0228a0001c0001t0020g0079a0001c0003t0001g0005others(11): Show | 14 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.80+3281A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602254 | ||||||
| chr8:144602276
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+3259A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602276 | ||||||
| chr8:144602279
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.80+3256C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602279 | ||||||
| chr8:144602286
|
C | CGT | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+3247_80+3248dup others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602286 | ||||||
| chr8:144602303
|
C | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+3232G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602303 | ||||||
| chr8:144602312
|
T | C | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+3223A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602312 | ||||||
| chr8:144602373
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.80+3162C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602373 | ||||||
| chr8:144602394
|
T | C | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+3141A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602394 | ||||||
| chr8:144602397
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.80+3138C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602397 | ||||||
| chr8:144602446
|
C | T | 20 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(17): Show | 20 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.80+3089G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602446 | ||||||
| chr8:144602474
|
C | T | 1 | a0001c0002t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.80+3061G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602474 | ||||||
| chr8:144602475
|
G | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.80+3060C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602475 | ||||||
| chr8:144602485
|
C | T | 119 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.80+3050G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602485 | ||||||
| chr8:144602561
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80+2974G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602561 | ||||||
| chr8:144602606
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.80+2929C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602606 | ||||||
| chr8:144602626
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG00639.hp1 HG01074.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.80+2909C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602626 | ||||||
| chr8:144602633
|
CGT | C | 69 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.80+2900_80+2901del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602633 | ||||||
| chr8:144602667
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+2868G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602667 | ||||||
| chr8:144602703
|
TGGA | T | 4 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+2829_80+2831del others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602703 | ||||||
| chr8:144602715
|
C | CGCTCGTG others(210): Show |
10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.80+2819_80+2820ins others(217): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602715 | ||||||
| chr8:144602715
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80+2820G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602715 | ||||||
| chr8:144602749
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80+2786A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602749 | ||||||
| chr8:144602773
|
T | C | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.80+2762A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602773 | ||||||
| chr8:144602773
|
TATGTGCA others(17): Show |
T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0117others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+2738_80+2761del others(24): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602773 | ||||||
| chr8:144602788
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0021g0062 | 2 | HG03453.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.80+2747C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602788 | ||||||
| chr8:144602802
|
G | T | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.80+2733C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602802 | ||||||
| chr8:144602804
|
A | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+2731T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602804 | ||||||
| chr8:144602811
|
C | CGT | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+2722_80+2723dup others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602811 | ||||||
| chr8:144602811
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+2724G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602811 | ||||||
| chr8:144602847
|
CGT | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0204others(2): Show | 5 | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+2686_80+2687del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602847 | ||||||
| chr8:144602874
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.80+2661C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602874 | ||||||
| chr8:144602877
|
T | C | 215 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.80+2658A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602877 | ||||||
| chr8:144602880
|
GGTGT | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG00558.hp1 HG03041.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+2651_80+2654del others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602880 | ||||||
| chr8:144602900
|
T | C | 1 | a0001c0002t0001g0137 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.80+2635A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602900 | ||||||
| chr8:144602903
|
CTG | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+2630_80+2631del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602903 | ||||||
| chr8:144602905
|
GTGTGTGT others(113): Show |
G | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+2510_80+2629del | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602905 | ||||||
| chr8:144602914
|
T | C | 2 | a0001c0001t0001g0236a0001c0002t0001g0124 | 2 | HG01346.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.80+2621A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602914 | ||||||
| chr8:144602991
|
A | G | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+2544T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144602991 | ||||||
| chr8:144603037
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.80+2498C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603037 | ||||||
| chr8:144603044
|
CGT | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80+2489_80+2490del others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603044 | ||||||
| chr8:144603058
|
C | T | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80+2477G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603058 | ||||||
| chr8:144603076
|
C | T | 1 | a0001c0003t0001g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.80+2459G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603076 | ||||||
| chr8:144603090
|
C | T | 52 | a0001c0001t0001g0024a0001c0001t0001g0136a0001c0001t0001g0146others(49): Show | 52 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.80+2445G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603090 | ||||||
| chr8:144603165
|
G | C | 9 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(6): Show | 9 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.80+2370C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603165 | ||||||
| chr8:144603168
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80+2367G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603168 | ||||||
| chr8:144603190
|
T | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.80+2345A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603190 | ||||||
| chr8:144603201
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.80+2334C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603201 | ||||||
| chr8:144603310
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | NA18963.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.80+2225A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603310 | ||||||
| chr8:144603312
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+2223G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603312 | ||||||
| chr8:144603341
|
A | C | 2 | a0001c0001t0001g0231a0001c0018t0001g0230 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.80+2194T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603341 | ||||||
| chr8:144603360
|
C | G | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+2175G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603360 | ||||||
| chr8:144603408
|
T | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80+2127A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603408 | ||||||
| chr8:144603424
|
C | A | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80+2111G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603424 | ||||||
| chr8:144603687
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80+1848G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603687 | ||||||
| chr8:144603687
|
C | CA | 22 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0049others(19): Show | 22 | HG01361.hp2 HG02145.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.80+1847dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603687 | ||||||
| chr8:144603687
|
C | CAAA | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.80+1845_80+1847dup others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603687 | ||||||
| chr8:144603687
|
CA | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0107a0001c0001t0001g0196others(3): Show | 6 | HG01167.hp1 HG01358.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+1847delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603687 | ||||||
| chr8:144603832
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+1703T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603832 | ||||||
| chr8:144603891
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80+1644C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603891 | ||||||
| chr8:144603896
|
ACAGGAT | A | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+1633_80+1638del others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603896 | ||||||
| chr8:144603903
|
C | T | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.80+1632G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144603903 | ||||||
| chr8:144604010
|
GCGAACAA others(12): Show |
G | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.80+1506_80+1524del others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604010 | ||||||
| chr8:144604102
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80+1433C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604102 | ||||||
| chr8:144604165
|
C | A | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.80+1370G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604165 | ||||||
| chr8:144604191
|
C | T | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+1344G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604191 | ||||||
| chr8:144604518
|
TAGGCATC others(8): Show |
T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80+1002_80+1016del others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604518 | ||||||
| chr8:144604672
|
T | C | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80+863A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604672 | ||||||
| chr8:144604739
|
A | G | 36 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(33): Show | 36 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.80+796T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144604739 | ||||||
| chr8:144605022
|
G | T | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.80+513C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605022 | ||||||
| chr8:144605074
|
C | G | 4 | a0001c0001t0001g0052a0001c0001t0012g0040a0001c0001t0014g0054others(1): Show | 4 | HG00438.hp1 NA18990.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+461G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605074 | ||||||
| chr8:144605211
|
T | C | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80+324A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605211 | ||||||
| chr8:144605243
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0044 | 2 | NA18944.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.80+292G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605243 | ||||||
| chr8:144605272
|
A | C | 1 | a0004c0009t0001g0008 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.80+263T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605272 | ||||||
| chr8:144605335
|
G | A | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.80+200C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605335 | ||||||
| chr8:144605373
|
A | G | 216 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.80+162T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | 144605373 | ||||||
| chr8:144605755
|
C | T | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-60G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144605755 | ||||||
| chr8:144605813
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-81-118G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144605813 | ||||||
| chr8:144605900
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-205G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144605900 | ||||||
| chr8:144605972
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-277T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144605972 | ||||||
| chr8:144605993
|
C | G | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-298G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144605993 | ||||||
| chr8:144606006
|
G | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-311C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606006 | ||||||
| chr8:144606011
|
T | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-81-316A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606011 | ||||||
| chr8:144606011
|
T | C | 213 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-81-316A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606011 | ||||||
| chr8:144606041
|
G | T | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-346C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606041 | ||||||
| chr8:144606235
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-540G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606235 | ||||||
| chr8:144606273
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-578G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606273 | ||||||
| chr8:144606388
|
A | G | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-693T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606388 | ||||||
| chr8:144606620
|
AGGAGGAG others(8): Show |
A | 1 | a0001c0002t0001g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-81-940_-81-926del others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606620 | ||||||
| chr8:144606675
|
G | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-980C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606675 | ||||||
| chr8:144606782
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-81-1087C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606782 | ||||||
| chr8:144606796
|
G | C | 1 | a0001c0007t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-81-1101C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606796 | ||||||
| chr8:144606810
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-81-1115C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606810 | ||||||
| chr8:144606932
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-81-1237T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606932 | ||||||
| chr8:144606997
|
C | CA | 26 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0132others(23): Show | 26 | HG00558.hp2 HG00609.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.-81-1303dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144606997 | ||||||
| chr8:144607074
|
T | C | 1 | a0001c0002t0001g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-81-1379A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607074 | ||||||
| chr8:144607235
|
C | CA | 39 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0144others(36): Show | 39 | HG00323.hp1 HG01169.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.-81-1541dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607235 | ||||||
| chr8:144607235
|
C | CAA | 7 | a0001c0001t0002g0241a0001c0001t0004g0150a0001c0001t0004g0156others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-1542_-81-1541d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607235 | ||||||
| chr8:144607235
|
CA | C | 7 | a0001c0001t0001g0177a0001c0001t0003g0023a0001c0001t0018g0022others(4): Show | 7 | HG00558.hp2 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-1541delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607235 | ||||||
| chr8:144607235
|
CAAAA | C | 10 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(7): Show | 10 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-1544_-81-1541d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607235 | ||||||
| chr8:144607328
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-1633A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607328 | ||||||
| chr8:144607344
|
A | G | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-1649T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607344 | ||||||
| chr8:144607599
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-81-1904T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607599 | ||||||
| chr8:144607763
|
G | A | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-81-2068C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607763 | ||||||
| chr8:144607773
|
C | T | 1 | a0001c0002t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-81-2078G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607773 | ||||||
| chr8:144607927
|
C | T | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-81-2232G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144607927 | ||||||
| chr8:144608084
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-81-2389C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608084 | ||||||
| chr8:144608132
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-2437C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608132 | ||||||
| chr8:144608156
|
C | CA | 18 | a0001c0001t0001g0034a0001c0001t0001g0049a0001c0001t0001g0052others(15): Show | 18 | HG01168.hp1 HG01175.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.-81-2462dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608156 | ||||||
| chr8:144608156
|
C | CAA | 17 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(14): Show | 17 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-81-2463_-81-2462d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608156 | ||||||
| chr8:144608156
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0002t0001g0080a0001c0002t0001g0098a0001c0002t0001g0162 | 3 | HG00741.hp1 NA18946.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-81-2471_-81-2462d others(12): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608156 | ||||||
| chr8:144608156
|
CAAAAAAA others(4): Show |
C | 74 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-81-2472_-81-2462d others(13): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608156 | ||||||
| chr8:144608156
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-81-2473_-81-2462d others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608156 | ||||||
| chr8:144608181
|
A | AT | 9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-2487_-81-2486i others(3): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608181 | ||||||
| chr8:144608181
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81-2486T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608181 | ||||||
| chr8:144608251
|
C | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-2556G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608251 | ||||||
| chr8:144608398
|
A | G | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-2703T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608398 | ||||||
| chr8:144608456
|
C | G | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-2761G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608456 | ||||||
| chr8:144608489
|
C | T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-81-2794G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608489 | ||||||
| chr8:144608742
|
C | G | 14 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(11): Show | 14 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-3047G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144608742 | ||||||
| chr8:144609026
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-3331T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609026 | ||||||
| chr8:144609122
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-3427G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609122 | ||||||
| chr8:144609245
|
T | C | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-3550A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609245 | ||||||
| chr8:144609276
|
T | C | 4 | a0001c0002t0001g0106a0001c0002t0001g0111a0001c0002t0001g0112others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-3581A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609276 | ||||||
| chr8:144609329
|
T | TTAATCTT others(326): Show |
1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-3635_-81-3634i others(335): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609329 | ||||||
| chr8:144609329
|
T | TTAATCTT others(328): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-3635_-81-3634i others(337): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609329 | ||||||
| chr8:144609392
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-3697A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609392 | ||||||
| chr8:144609397
|
C | CT | 19 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0052others(16): Show | 19 | HG00741.hp1 HG00741.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81-3703dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609397 | ||||||
| chr8:144609397
|
C | CTT | 11 | a0001c0001t0001g0228a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-3704_-81-3703d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609397 | ||||||
| chr8:144609397
|
CT | C | 9 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0221others(6): Show | 9 | HG02486.hp2 HG02572.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-3703delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609397 | ||||||
| chr8:144609455
|
G | A | 1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-81-3760C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609455 | ||||||
| chr8:144609556
|
T | C | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-81-3861A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609556 | ||||||
| chr8:144609683
|
TGAGCCAC others(5): Show |
T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-4000_-81-3989d others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609683 | ||||||
| chr8:144609691
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-3996G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609691 | ||||||
| chr8:144609895
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0211 | 2 | HG02055.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-81-4200A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609895 | ||||||
| chr8:144609986
|
A | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-81-4291T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144609986 | ||||||
| chr8:144610040
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-81-4345G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610040 | ||||||
| chr8:144610041
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-4346C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610041 | ||||||
| chr8:144610066
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-81-4371T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610066 | ||||||
| chr8:144610243
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-4548C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610243 | ||||||
| chr8:144610303
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-81-4608T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610303 | ||||||
| chr8:144610580
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-4885G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610580 | ||||||
| chr8:144610711
|
C | CA | 47 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(44): Show | 47 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-81-5017dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610711 | ||||||
| chr8:144610724
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-81-5029A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610724 | ||||||
| chr8:144610802
|
G | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-5107C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610802 | ||||||
| chr8:144610842
|
A | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-81-5147T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610842 | ||||||
| chr8:144610870
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-5175C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610870 | ||||||
| chr8:144610961
|
C | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-5266G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144610961 | ||||||
| chr8:144611138
|
T | C | 13 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-5443A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611138 | ||||||
| chr8:144611440
|
G | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81-5745C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611440 | ||||||
| chr8:144611456
|
A | G | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-5761T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611456 | ||||||
| chr8:144611483
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-81-5788G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611483 | ||||||
| chr8:144611516
|
ATAGCTCT others(5): Show |
A | 4 | a0001c0001t0001g0107a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-5833_-81-5822d others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611516 | ||||||
| chr8:144611550
|
T | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-5855A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611550 | ||||||
| chr8:144611593
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(8): Show | 11 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81-5898A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611593 | ||||||
| chr8:144611958
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-6263C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611958 | ||||||
| chr8:144611994
|
A | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-6299T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144611994 | ||||||
| chr8:144612008
|
T | TA | 15 | a0001c0001t0001g0016a0001c0001t0003g0023a0001c0001t0003g0063others(12): Show | 15 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-81-6314dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612008 | ||||||
| chr8:144612105
|
A | C | 8 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-6410T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612105 | ||||||
| chr8:144612122
|
A | AGTGAGCC others(137): Show |
1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-6428_-81-6427i others(146): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612122 | ||||||
| chr8:144612122
|
A | AGTGAGCC others(41): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-81-6475_-81-6428d others(50): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612122 | ||||||
| chr8:144612122
|
AGTGAGCC others(137): Show |
A | 31 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0228others(28): Show | 31 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-81-6571_-81-6428d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612122 | ||||||
| chr8:144612132
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-6437C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612132 | ||||||
| chr8:144612148
|
TCCAGCCA others(89): Show |
T | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-6549_-81-6454d others(98): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612148 | ||||||
| chr8:144612244
|
A | ACCAGCCA others(41): Show |
3 | a0001c0001t0001g0016a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | HG02717.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-81-6597_-81-6550d others(50): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612244 | ||||||
| chr8:144612244
|
A | T | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-6549T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612244 | ||||||
| chr8:144612244
|
ACCAGCCA others(185): Show |
A | 9 | a0001c0001t0001g0238a0001c0001t0007g0018a0001c0004t0006g0069others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-6741_-81-6550d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612244 | ||||||
| chr8:144612258
|
CAGAGTGA others(139): Show |
C | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-6709_-81-6564d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612258 | ||||||
| chr8:144612388
|
A | ACCAGCCA others(41): Show |
4 | a0001c0001t0001g0016a0001c0001t0001g0179a0001c0001t0002g0234others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-6741_-81-6694d others(50): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612388 | ||||||
| chr8:144612388
|
A | ACCAGCCA others(233): Show |
1 | a0001c0002t0001g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-81-6694_-81-6693i others(242): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612388 | ||||||
| chr8:144612388
|
A | ACCAGCCA others(233): Show |
3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-6694_-81-6693i others(242): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612388 | ||||||
| chr8:144612388
|
A | ACCAGCCA others(233): Show |
168 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-81-6933_-81-6694d others(242): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612388 | ||||||
| chr8:144612388
|
A | ACCAGCCA others(281): Show |
1 | a0001c0001t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-81-6981_-81-6694d others(290): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612388 | ||||||
| chr8:144612474
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-6779C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612474 | ||||||
| chr8:144612525
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02027.hp2 HG02132.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-6830C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612525 | ||||||
| chr8:144612564
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-6869C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612564 | ||||||
| chr8:144612580
|
A | ACCAGCCA others(281): Show |
1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-81-6886_-81-6885i others(290): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612580 | ||||||
| chr8:144612580
|
A | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-6885T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612580 | ||||||
| chr8:144612628
|
T | TCCAGCCA others(185): Show |
1 | a0001c0002t0001g0216 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-81-6934_-81-6933i others(194): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612628 | ||||||
| chr8:144612632
|
G | A | 50 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(47): Show | 50 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-81-6937C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612632 | ||||||
| chr8:144612687
|
C | CGACAGAG others(233): Show |
1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-81-6993_-81-6992i others(242): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612687 | ||||||
| chr8:144612765
|
G | GCTGCACT others(281): Show |
1 | a0001c0001t0002g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-81-7071_-81-7070i others(290): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612765 | ||||||
| chr8:144612784
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-81-7089C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612784 | ||||||
| chr8:144612794
|
A | G | 5 | a0001c0002t0001g0090a0001c0002t0001g0094a0001c0002t0001g0108others(2): Show | 5 | HG00609.hp1 HG01952.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-7099T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612794 | ||||||
| chr8:144612810
|
A | G | 10 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-7115T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612810 | ||||||
| chr8:144612979
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18941.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-81-7284C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144612979 | ||||||
| chr8:144613233
|
A | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-7538T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144613233 | ||||||
| chr8:144613373
|
A | G | 50 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0100others(47): Show | 50 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-81-7678T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144613373 | ||||||
| chr8:144613490
|
G | GT | 20 | a0001c0001t0001g0049a0001c0001t0001g0135a0001c0001t0001g0223others(17): Show | 20 | HG01192.hp2 HG02109.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-81-7796dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144613490 | ||||||
| chr8:144613673
|
C | T | 58 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0151others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-81-7978G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144613673 | ||||||
| chr8:144613822
|
C | A | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-81-8127G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144613822 | ||||||
| chr8:144614291
|
G | T | 1 | a0001c0002t0001g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-81-8596C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614291 | ||||||
| chr8:144614354
|
A | AT | 17 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0149others(14): Show | 17 | HG00280.hp1 HG00408.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-8660dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614354 | ||||||
| chr8:144614354
|
A | ATT | 7 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(4): Show | 7 | HG02622.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-8661_-81-8660d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614354 | ||||||
| chr8:144614354
|
A | ATTT | 6 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0004g0237others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-8662_-81-8660d others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614354 | ||||||
| chr8:144614354
|
A | ATTTT | 9 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(6): Show | 9 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-8663_-81-8660d others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614354 | ||||||
| chr8:144614354
|
AT | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0197a0001c0001t0001g0236others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-8660delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614354 | ||||||
| chr8:144614358
|
T | C | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-8663A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614358 | ||||||
| chr8:144614411
|
G | A | 4 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-8716C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614411 | ||||||
| chr8:144614421
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-81-8726G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614421 | ||||||
| chr8:144614509
|
C | T | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-81-8814G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614509 | ||||||
| chr8:144614517
|
T | A | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-8822A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614517 | ||||||
| chr8:144614604
|
T | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-8909A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614604 | ||||||
| chr8:144614622
|
G | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-8927C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614622 | ||||||
| chr8:144614653
|
C | T | 1 | a0001c0006t0001g0181 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-81-8958G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614653 | ||||||
| chr8:144614741
|
G | C | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-9046C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614741 | ||||||
| chr8:144614929
|
T | G | 18 | a0001c0001t0001g0228a0001c0003t0001g0005a0001c0003t0001g0012others(15): Show | 18 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.-81-9234A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614929 | ||||||
| chr8:144614992
|
C | T | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-9297G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144614992 | ||||||
| chr8:144615029
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-9334G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615029 | ||||||
| chr8:144615235
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-81-9540G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615235 | ||||||
| chr8:144615294
|
T | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-9599A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615294 | ||||||
| chr8:144615341
|
A | C | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-81-9646T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615341 | ||||||
| chr8:144615395
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-81-9700G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615395 | ||||||
| chr8:144615588
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-81-9893T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615588 | ||||||
| chr8:144615702
|
C | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-10007G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615702 | ||||||
| chr8:144615766
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-81-10071C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615766 | ||||||
| chr8:144615814
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-81-10119C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144615814 | ||||||
| chr8:144616322
|
T | C | 216 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-81-10627A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616322 | ||||||
| chr8:144616470
|
G | A | 11 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-10775C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616470 | ||||||
| chr8:144616496
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-81-10801C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616496 | ||||||
| chr8:144616545
|
C | G | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-81-10850G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616545 | ||||||
| chr8:144616593
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-10898G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616593 | ||||||
| chr8:144616727
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-81-11032C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616727 | ||||||
| chr8:144616749
|
G | A | 6 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-11054C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144616749 | ||||||
| chr8:144617080
|
G | T | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-81-11385C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617080 | ||||||
| chr8:144617168
|
C | T | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-81-11473G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617168 | ||||||
| chr8:144617185
|
C | T | 1 | a0001c0002t0001g0114 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-81-11490G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617185 | ||||||
| chr8:144617205
|
T | TA | 19 | a0001c0002t0001g0124a0001c0002t0001g0214a0001c0003t0001g0012others(16): Show | 19 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.-81-11511dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617205 | ||||||
| chr8:144617206
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-81-11511T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617206 | ||||||
| chr8:144617208
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-11513T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617208 | ||||||
| chr8:144617349
|
G | A | 20 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(17): Show | 20 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-11654C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617349 | ||||||
| chr8:144617425
|
A | ACAAACCA others(23): Show |
1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-81-11760_-81-1173 others(34): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617425 | ||||||
| chr8:144617451
|
C | T | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-11756G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617451 | ||||||
| chr8:144617574
|
A | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0170 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-81-11879T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617574 | ||||||
| chr8:144617585
|
C | CA | 10 | a0001c0001t0001g0163a0001c0001t0001g0172a0001c0001t0004g0237others(7): Show | 10 | HG02135.hp2 HG02572.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-11891dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617585 | ||||||
| chr8:144617585
|
CA | C | 16 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0002t0001g0025others(13): Show | 16 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-81-11891delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617585 | ||||||
| chr8:144617760
|
T | C | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-12065A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617760 | ||||||
| chr8:144617958
|
T | A | 1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-81-12263A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144617958 | ||||||
| chr8:144618073
|
C | T | 12 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-12378G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618073 | ||||||
| chr8:144618085
|
A | C | 1 | a0001c0001t0007g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-81-12390T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618085 | ||||||
| chr8:144618092
|
T | C | 2 | a0001c0007t0017g0019a0003c0011t0001g0072 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-12397A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618092 | ||||||
| chr8:144618173
|
A | G | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-81-12478T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618173 | ||||||
| chr8:144618261
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-81-12566C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618261 | ||||||
| chr8:144618306
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-12611C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618306 | ||||||
| chr8:144618394
|
T | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-12699A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618394 | ||||||
| chr8:144618551
|
T | C | 2 | a0001c0002t0001g0098a0001c0002t0019g0125 | 2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81-12856A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618551 | ||||||
| chr8:144618592
|
GCCTCAGC others(14): Show |
G | 2 | a0001c0002t0001g0129a0001c0002t0001g0130 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-81-12918_-81-1289 others(25): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618592 | ||||||
| chr8:144618654
|
C | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-81-12959G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618654 | ||||||
| chr8:144618664
|
G | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0145a0001c0001t0002g0170 | 3 | HG02280.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-81-12969C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618664 | ||||||
| chr8:144618716
|
T | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-81-13021A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618716 | ||||||
| chr8:144618748
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-81-13053C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618748 | ||||||
| chr8:144618752
|
C | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0139a0001c0001t0002g0145others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-13057G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144618752 | ||||||
| chr8:144619275
|
C | T | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-13580G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619275 | ||||||
| chr8:144619394
|
CCATGTG | C | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-13705_-81-1370 others(10): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619394 | ||||||
| chr8:144619396
|
A | G | 204 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-81-13701T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619396 | ||||||
| chr8:144619401
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-13706G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619401 | ||||||
| chr8:144619402
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-81-13707C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619402 | ||||||
| chr8:144619417
|
C | T | 16 | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(13): Show | 16 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-81-13722G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619417 | ||||||
| chr8:144619421
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-81-13726T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619421 | ||||||
| chr8:144619502
|
C | G | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-81-13807G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619502 | ||||||
| chr8:144619537
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-13842G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619537 | ||||||
| chr8:144619552
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-81-13857C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619552 | ||||||
| chr8:144619605
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-81-13910A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619605 | ||||||
| chr8:144619608
|
ATGTCCGT others(27): Show |
A | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-81-13947_-81-1391 others(38): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619608 | ||||||
| chr8:144619717
|
CAT | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01981.hp2 NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-81-14024_-81-1402 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619717 | ||||||
| chr8:144619727
|
C | T | 67 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-81-14032G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619727 | ||||||
| chr8:144619733
|
C | T | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81-14038G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619733 | ||||||
| chr8:144619763
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-14068G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619763 | ||||||
| chr8:144619785
|
C | T | 1 | a0001c0002t0001g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-81-14090G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619785 | ||||||
| chr8:144619791
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-81-14096T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619791 | ||||||
| chr8:144619796
|
G | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-14101C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619796 | ||||||
| chr8:144619801
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-81-14106G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619801 | ||||||
| chr8:144619802
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-81-14107C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619802 | ||||||
| chr8:144619871
|
A | T | 51 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-81-14176T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619871 | ||||||
| chr8:144619907
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-81-14212G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144619907 | ||||||
| chr8:144620013
|
C | T | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-81-14318G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620013 | ||||||
| chr8:144620051
|
C | T | 2 | a0001c0002t0001g0140a0001c0002t0001g0222 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-81-14356G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620051 | ||||||
| chr8:144620064
|
G | T | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-81-14369C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620064 | ||||||
| chr8:144620080
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | HG02055.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-14385C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620080 | ||||||
| chr8:144620126
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-81-14431G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620126 | ||||||
| chr8:144620141
|
G | A | 1 | a0001c0001t0008g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-81-14446C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620141 | ||||||
| chr8:144620198
|
C | T | 7 | a0001c0001t0001g0151a0001c0001t0004g0150a0001c0001t0004g0152others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-14503G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620198 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(33): Show |
6 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0005g0243others(3): Show | 6 | HG00323.hp2 HG01975.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-14571_-81-1453 others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(73): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0001g0141others(10): Show | 13 | HG00609.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-14611_-81-1453 others(84): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(113): Show |
3 | a0001c0001t0001g0149a0001c0001t0001g0172a0001c0001t0007g0018 | 3 | HG02135.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-81-14651_-81-1453 others(124): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(153): Show |
1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-81-14691_-81-1453 others(164): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(193): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-81-14731_-81-1453 others(204): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(354): Show |
9 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0226others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-14532_-81-1453 others(365): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(434): Show |
1 | a0001c0001t0001g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-81-14532_-81-1453 others(445): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(353): Show |
1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-81-14532_-81-1453 others(364): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
T | TGTGTGTG others(706): Show |
4 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088others(1): Show | 4 | HG00639.hp2 HG02683.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-14532_-81-1453 others(717): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
TGTGTGTG others(33): Show |
T | 24 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0134others(21): Show | 24 | HG00280.hp2 HG00438.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-81-14571_-81-1453 others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
TGTGTGTG others(73): Show |
T | 9 | a0001c0001t0001g0202a0001c0001t0001g0228a0001c0001t0002g0131others(6): Show | 9 | HG01074.hp2 HG01099.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-14611_-81-1453 others(84): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
TGTGTGTG others(113): Show |
T | 15 | a0001c0001t0001g0043a0001c0001t0003g0063a0001c0001t0003g0071others(12): Show | 15 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-81-14651_-81-1453 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620226
|
TGTGTGTG others(153): Show |
T | 16 | a0001c0001t0003g0068a0001c0001t0020g0079a0001c0002t0001g0103others(13): Show | 16 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.-81-14691_-81-1453 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620226 | ||||||
| chr8:144620268
|
T | TGTGTGCC others(233): Show |
1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-81-14813_-81-1457 others(244): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620268 | ||||||
| chr8:144620285
|
T | TAGCCTGT others(194): Show |
1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81-14791_-81-1459 others(205): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620285 | ||||||
| chr8:144620365
|
T | TAGCCTGT others(74): Show |
1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-14751_-81-1467 others(85): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620365 | ||||||
| chr8:144620388
|
TGTGTGCC others(113): Show |
T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-14813_-81-1469 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620388 | ||||||
| chr8:144620427
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-14732C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620427 | ||||||
| chr8:144620428
|
T | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-14733A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620428 | ||||||
| chr8:144620428
|
TGTGTGCC others(73): Show |
T | 5 | a0001c0001t0001g0027a0001c0001t0001g0196a0001c0001t0001g0198others(2): Show | 5 | HG01071.hp1 HG01358.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-14813_-81-1473 others(84): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620428 | ||||||
| chr8:144620468
|
TGTGTGCC others(33): Show |
T | 2 | a0001c0002t0001g0214a0001c0017t0001g0064 | 2 | NA18990.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-81-14813_-81-1477 others(44): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620468 | ||||||
| chr8:144620507
|
A | G | 13 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0204others(10): Show | 13 | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-14812T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620507 | ||||||
| chr8:144620508
|
C | T | 13 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0204others(10): Show | 13 | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-14813G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620508 | ||||||
| chr8:144620509
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81-14814C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620509 | ||||||
| chr8:144620538
|
A | G | 4 | a0001c0001t0020g0079a0001c0002t0001g0129a0001c0002t0001g0130others(1): Show | 4 | HG02109.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-14843T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620538 | ||||||
| chr8:144620556
|
C | CGT | 50 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0132others(47): Show | 50 | HG00408.hp2 HG00558.hp2 HG01975.hp2 others(47): Show |
intron_variant | MODIFIER | c.-81-14863_-81-1486 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620556 | ||||||
| chr8:144620730
|
G | A | 67 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-81-15035C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620730 | ||||||
| chr8:144620731
|
T | C | 67 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-81-15036A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620731 | ||||||
| chr8:144620748
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-81-15053G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620748 | ||||||
| chr8:144620782
|
G | A | 96 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0032others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-81-15087C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620782 | ||||||
| chr8:144620838
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81-15143C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620838 | ||||||
| chr8:144620864
|
G | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0225a0001c0001t0001g0227others(6): Show | 9 | HG01975.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-15169C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620864 | ||||||
| chr8:144620883
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-81-15188C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144620883 | ||||||
| chr8:144621018
|
C | T | 3 | a0001c0002t0001g0083a0001c0002t0001g0167a0001c0002t0001g0169 | 3 | HG01192.hp2 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-81-15323G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621018 | ||||||
| chr8:144621185
|
T | C | 148 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-81-15490A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621185 | ||||||
| chr8:144621197
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-81-15502T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621197 | ||||||
| chr8:144621294
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-81-15599T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621294 | ||||||
| chr8:144621323
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-81-15628C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621323 | ||||||
| chr8:144621446
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-15751C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621446 | ||||||
| chr8:144621473
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81-15778C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621473 | ||||||
| chr8:144621480
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-81-15785C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621480 | ||||||
| chr8:144621490
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-15795C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621490 | ||||||
| chr8:144621586
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-15891C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621586 | ||||||
| chr8:144621739
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-81-16044C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144621739 | ||||||
| chr8:144622132
|
C | T | 173 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-81-16437G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622132 | ||||||
| chr8:144622297
|
T | C | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-16602A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622297 | ||||||
| chr8:144622370
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-16675C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622370 | ||||||
| chr8:144622500
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-16805G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622500 | ||||||
| chr8:144622583
|
C | A | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0204others(2): Show | 5 | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-16888G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622583 | ||||||
| chr8:144622591
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-81-16896T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622591 | ||||||
| chr8:144622617
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-81-16922C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622617 | ||||||
| chr8:144622752
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-81-17057C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622752 | ||||||
| chr8:144622770
|
AG | A | 5 | a0001c0005t0001g0006a0001c0005t0001g0010a0001c0005t0001g0011others(2): Show | 5 | HG00639.hp1 HG01168.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-17076delC | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622770 | ||||||
| chr8:144622908
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-17213C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622908 | ||||||
| chr8:144622963
|
A | C | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-17268T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144622963 | ||||||
| chr8:144623333
|
A | G | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-17638T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623333 | ||||||
| chr8:144623476
|
G | C | 4 | a0001c0006t0001g0171a0001c0006t0001g0181a0001c0006t0001g0182others(1): Show | 4 | HG00099.hp1 HG00741.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-17781C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623476 | ||||||
| chr8:144623559
|
C | T | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-17864G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623559 | ||||||
| chr8:144623567
|
C | A | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-17872G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623567 | ||||||
| chr8:144623710
|
C | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-18015G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623710 | ||||||
| chr8:144623778
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-18083C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623778 | ||||||
| chr8:144623824
|
A | G | 211 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-81-18129T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623824 | ||||||
| chr8:144623829
|
G | C | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-18134C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623829 | ||||||
| chr8:144623888
|
G | A | 198 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-81-18193C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623888 | ||||||
| chr8:144623998
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-18303A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144623998 | ||||||
| chr8:144624282
|
T | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-18587A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624282 | ||||||
| chr8:144624300
|
A | G | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-18605T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624300 | ||||||
| chr8:144624363
|
A | AAAG | 216 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-81-18671_-81-1866 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624363 | ||||||
| chr8:144624392
|
C | T | 211 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-81-18697G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624392 | ||||||
| chr8:144624580
|
TCACTGCA others(197): Show |
T | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-19089_-81-1888 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624580 | ||||||
| chr8:144624609
|
G | C | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-18914C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624609 | ||||||
| chr8:144624617
|
G | A | 1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-81-18922C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624617 | ||||||
| chr8:144624617
|
G | C | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-18922C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624617 | ||||||
| chr8:144624617
|
GGTTCACG others(656): Show |
G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-19585_-81-1892 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624617 | ||||||
| chr8:144624617
|
GGTTCACG others(860): Show |
G | 4 | a0001c0001t0001g0203a0001c0006t0001g0171a0001c0006t0001g0181others(1): Show | 4 | HG00741.hp2 HG01081.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-19789_-81-1892 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624617 | ||||||
| chr8:144624617
|
GGTTCACG others(1676): Show |
G | 1 | a0001c0006t0001g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-81-20605_-81-1892 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624617 | ||||||
| chr8:144624631
|
T | C | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-18936A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624631 | ||||||
| chr8:144624631
|
TCACTGCA others(350): Show |
T | 3 | a0001c0001t0002g0138a0001c0002t0001g0167a0001c0016t0001g0091 | 3 | HG01081.hp1 HG01975.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-81-19293_-81-1893 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624631 | ||||||
| chr8:144624631
|
TCACTGCA others(605): Show |
T | 3 | a0001c0002t0001g0015a0001c0002t0001g0115a0001c0017t0001g0064 | 3 | HG02300.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-81-19548_-81-1893 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624631 | ||||||
| chr8:144624631
|
TCACTGCA others(1574): Show |
T | 11 | a0001c0001t0003g0023a0001c0001t0003g0068a0001c0001t0003g0071others(8): Show | 11 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-20517_-81-1893 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624631 | ||||||
| chr8:144624649
|
T | G | 181 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(178): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.-81-18954A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624649 | ||||||
| chr8:144624668
|
G | C | 2 | a0001c0001t0003g0063a0001c0001t0007g0018 | 2 | HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-81-18973C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624668 | ||||||
| chr8:144624668
|
GGTTCACG others(809): Show |
G | 72 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-81-19789_-81-1897 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624668 | ||||||
| chr8:144624682
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0001t0012g0040 | 3 | HG02451.hp2 HG02717.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-81-18987A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624682
|
TCACTGCA others(95): Show |
T | 4 | a0001c0002t0001g0003a0001c0002t0001g0124a0002c0008t0001g0067others(1): Show | 4 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-19089_-81-1898 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624682
|
TCACTGCA others(554): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-81-19548_-81-1898 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624682
|
TCACTGCA others(605): Show |
T | 78 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-81-19599_-81-1898 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624682
|
TCACTGCA others(656): Show |
T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-19650_-81-1898 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624682
|
TCACTGCA others(1115): Show |
T | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-20109_-81-1898 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624682 | ||||||
| chr8:144624700
|
GCCCCTGT others(299): Show |
G | 14 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(11): Show | 14 | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-19311_-81-1900 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624700 | ||||||
| chr8:144624711
|
G | C | 1 | a0001c0001t0003g0063 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-81-19016C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624711 | ||||||
| chr8:144624711
|
GGCGGCCC others(1217): Show |
G | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-20240_-81-1901 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624711 | ||||||
| chr8:144624716
|
CCCGGTTC others(1573): Show |
C | 1 | a0001c0001t0003g0063 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-81-20601_-81-1902 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624716 | ||||||
| chr8:144624719
|
G | C | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-19024C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624719 | ||||||
| chr8:144624733
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 8 | HG02109.hp1 HG02132.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-19038A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624733 | ||||||
| chr8:144624733
|
TCACTGCA others(197): Show |
T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-19242_-81-1903 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624733 | ||||||
| chr8:144624762
|
C | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81-19067G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624762 | ||||||
| chr8:144624770
|
C | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0232others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-19075G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624770 | ||||||
| chr8:144624784
|
CCACTGCA others(707): Show |
C | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0232 | 3 | HG02109.hp1 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-81-19803_-81-1909 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624784 | ||||||
| chr8:144624802
|
G | T | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-81-19107C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624802 | ||||||
| chr8:144624813
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-81-19118C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624813 | ||||||
| chr8:144624821
|
C | G | 3 | a0001c0001t0001g0016a0001c0002t0001g0020a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-81-19126G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624821 | ||||||
| chr8:144624835
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-81-19140G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624835 | ||||||
| chr8:144624853
|
T | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0233a0001c0001t0002g0241others(5): Show | 8 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-19158A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624853 | ||||||
| chr8:144624872
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-81-19177C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624872 | ||||||
| chr8:144624872
|
GGTTCACG others(248): Show |
G | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-81-19432_-81-1917 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624872 | ||||||
| chr8:144624886
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-19191G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624886 | ||||||
| chr8:144624915
|
G | C | 5 | a0001c0002t0001g0003a0001c0002t0001g0124a0001c0007t0001g0017others(2): Show | 5 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-19220C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624915 | ||||||
| chr8:144624923
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0233 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-81-19228G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624923 | ||||||
| chr8:144624937
|
C | T | 6 | a0001c0001t0002g0241a0001c0002t0001g0003a0001c0002t0001g0124others(3): Show | 6 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-19242G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624937 | ||||||
| chr8:144624955
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-19260C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624955 | ||||||
| chr8:144624965
|
C | T | 1 | a0001c0002t0001g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-81-19270G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624965 | ||||||
| chr8:144624966
|
GGCGGCCC others(758): Show |
G | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-81-20036_-81-1927 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624966 | ||||||
| chr8:144624968
|
C | T | 2 | a0002c0008t0001g0067a0002c0008t0001g0142 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-81-19273G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624968 | ||||||
| chr8:144624974
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-19279G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624974 | ||||||
| chr8:144624974
|
CGTTCACG others(95): Show |
C | 4 | a0001c0002t0001g0003a0001c0002t0001g0124a0002c0008t0001g0067others(1): Show | 4 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-19381_-81-1928 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144624974 | ||||||
| chr8:144625006
|
T | G | 6 | a0001c0001t0001g0016a0001c0001t0002g0138a0001c0001t0007g0018others(3): Show | 6 | HG01081.hp1 HG01975.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-19311A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625006 | ||||||
| chr8:144625017
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-19322C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625017 | ||||||
| chr8:144625025
|
G | C | 20 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0148others(17): Show | 20 | HG01081.hp1 HG01168.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81-19330C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625025 | ||||||
| chr8:144625025
|
GGTTCACG others(605): Show |
G | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-19942_-81-1933 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625025 | ||||||
| chr8:144625076
|
GGTTCACG others(44): Show |
G | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0016g0105others(4): Show | 7 | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-19432_-81-1938 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625076 | ||||||
| chr8:144625090
|
C | T | 5 | a0001c0002t0001g0003a0001c0002t0001g0124a0001c0007t0017g0019others(2): Show | 5 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-19395G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625090 | ||||||
| chr8:144625119
|
G | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0238a0001c0001t0002g0138others(8): Show | 11 | HG01081.hp1 HG01975.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-19424C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625119 | ||||||
| chr8:144625141
|
C | CCACTGCA others(197): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-81-19447_-81-1944 others(208): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625141 | ||||||
| chr8:144625141
|
C | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0238others(10): Show | 13 | HG01081.hp1 HG01975.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-19446G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625141 | ||||||
| chr8:144625169
|
C | T | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-81-19474G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625169 | ||||||
| chr8:144625170
|
G | C | 8 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0016g0105others(5): Show | 8 | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-19475C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625170 | ||||||
| chr8:144625178
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0007g0018 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-81-19483G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625178 | ||||||
| chr8:144625192
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(18): Show | 21 | HG00558.hp2 HG01081.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81-19497G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625192 | ||||||
| chr8:144625210
|
G | T | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-19515C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625210 | ||||||
| chr8:144625221
|
G | C | 3 | a0001c0001t0001g0024a0001c0002t0001g0021a0001c0002t0001g0025 | 3 | HG03041.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-19526C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625221 | ||||||
| chr8:144625229
|
C | G | 39 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.-81-19534G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625229 | ||||||
| chr8:144625243
|
C | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(7): Show | 10 | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-19548G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625243 | ||||||
| chr8:144625261
|
G | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0124 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-81-19566C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625261 | ||||||
| chr8:144625272
|
G | C | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-19577C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625272 | ||||||
| chr8:144625280
|
C | G | 9 | a0001c0002t0001g0003a0001c0002t0001g0015a0001c0002t0001g0020others(6): Show | 9 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-19585G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625280 | ||||||
| chr8:144625294
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0238others(11): Show | 14 | HG00558.hp2 HG01081.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-19599G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625294 | ||||||
| chr8:144625307
|
C | T | 2 | a0002c0008t0001g0067a0002c0008t0001g0142 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-81-19612G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625307 | ||||||
| chr8:144625312
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-19617C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625312 | ||||||
| chr8:144625323
|
G | C | 4 | a0001c0002t0001g0003a0001c0002t0001g0124a0002c0008t0001g0067others(1): Show | 4 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-19628C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625323 | ||||||
| chr8:144625323
|
G | GGCGGCCC others(248): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-19629_-81-1962 others(259): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625323 | ||||||
| chr8:144625331
|
C | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0184others(6): Show | 9 | HG01081.hp1 HG01975.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-19636G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625331 | ||||||
| chr8:144625345
|
C | T | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0238others(10): Show | 13 | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-19650G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625345 | ||||||
| chr8:144625345
|
CCACTGCA others(146): Show |
C | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-81-19803_-81-1965 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625345 | ||||||
| chr8:144625345
|
CCACTGCA others(299): Show |
C | 3 | a0001c0001t0002g0138a0001c0002t0001g0167a0001c0016t0001g0091 | 3 | HG01081.hp1 HG01975.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-81-19956_-81-1965 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625345 | ||||||
| chr8:144625374
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-81-19679C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625374 | ||||||
| chr8:144625382
|
C | G | 105 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0061others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-81-19687G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625382 | ||||||
| chr8:144625396
|
C | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0184a0001c0002t0001g0003others(5): Show | 8 | HG00558.hp2 HG01346.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-19701G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625396 | ||||||
| chr8:144625414
|
G | T | 11 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0238others(8): Show | 11 | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-19719C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625414 | ||||||
| chr8:144625414
|
GCCCCTGT others(452): Show |
G | 1 | a0001c0002t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-81-20178_-81-1972 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625414 | ||||||
| chr8:144625425
|
G | C | 89 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-81-19730C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625425 | ||||||
| chr8:144625425
|
GGCGGCCC others(44): Show |
G | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-19781_-81-1973 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625425 | ||||||
| chr8:144625433
|
G | C | 93 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0061others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-81-19738C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625433 | ||||||
| chr8:144625447
|
T | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0044others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-81-19752A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625447 | ||||||
| chr8:144625465
|
T | G | 109 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0065others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-81-19770A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625465 | ||||||
| chr8:144625475
|
C | T | 49 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0100others(46): Show | 49 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.-81-19780G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625475 | ||||||
| chr8:144625476
|
C | G | 93 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0065others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-81-19781G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625476 | ||||||
| chr8:144625484
|
C | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0231a0001c0001t0007g0018others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-19789G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625484 | ||||||
| chr8:144625498
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0001g0208others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-19803A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625498 | ||||||
| chr8:144625498
|
TCACTGCA others(95): Show |
T | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0098others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-19905_-81-1980 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625498 | ||||||
| chr8:144625498
|
TCACTGCA others(197): Show |
T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-20007_-81-1980 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625498 | ||||||
| chr8:144625527
|
G | C | 11 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81-19832C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625527 | ||||||
| chr8:144625527
|
GGCGGCCC others(197): Show |
G | 5 | a0001c0001t0001g0238a0001c0001t0004g0237a0001c0001t0007g0239others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-20036_-81-1983 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625527 | ||||||
| chr8:144625535
|
C | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0043others(3): Show | 6 | HG02647.hp2 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-19840G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625535 | ||||||
| chr8:144625549
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0001g0223others(19): Show | 22 | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81-19854G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625549 | ||||||
| chr8:144625567
|
G | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-19872C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625567 | ||||||
| chr8:144625567
|
GCCCCTGT others(299): Show |
G | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-81-20178_-81-1987 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625567 | ||||||
| chr8:144625578
|
G | C | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-19883C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625578 | ||||||
| chr8:144625586
|
G | C | 83 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0043others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-81-19891C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625586 | ||||||
| chr8:144625586
|
GGTTCACG others(44): Show |
G | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-19942_-81-1989 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625586 | ||||||
| chr8:144625591
|
A | G | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-81-19896T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625591 | ||||||
| chr8:144625600
|
C | T | 82 | a0001c0001t0001g0024a0001c0001t0001g0061a0001c0001t0001g0065others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-81-19905G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625600 | ||||||
| chr8:144625618
|
G | T | 6 | a0001c0001t0001g0184a0001c0002t0001g0003a0001c0002t0001g0124others(3): Show | 6 | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-19923C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625618 | ||||||
| chr8:144625629
|
G | C | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(73): Show | 76 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-81-19934C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625629 | ||||||
| chr8:144625629
|
GGCGGCCC others(95): Show |
G | 4 | a0001c0001t0001g0024a0001c0001t0001g0231a0001c0002t0001g0025others(1): Show | 4 | HG02647.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-20036_-81-1993 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625629 | ||||||
| chr8:144625632
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-81-19937C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625632 | ||||||
| chr8:144625637
|
C | G | 90 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0065others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-81-19942G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625637 | ||||||
| chr8:144625643
|
C | T | 1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-81-19948G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625643 | ||||||
| chr8:144625651
|
T | C | 83 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0052others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-81-19956A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625651 | ||||||
| chr8:144625651
|
TCACTGCA others(44): Show |
T | 4 | a0001c0002t0001g0003a0001c0002t0001g0124a0001c0010t0001g0009others(1): Show | 4 | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-20007_-81-1995 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625651 | ||||||
| chr8:144625669
|
G | GCCCCTGT others(95): Show |
1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-19975_-81-1997 others(106): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625669 | ||||||
| chr8:144625669
|
G | T | 71 | a0001c0001t0001g0016a0001c0001t0001g0065a0001c0001t0001g0097others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-81-19974C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625669 | ||||||
| chr8:144625680
|
G | C | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-81-19985C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625680 | ||||||
| chr8:144625680
|
GGCGGCCC others(44): Show |
G | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-81-20036_-81-1998 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625680 | ||||||
| chr8:144625680
|
GGCGGCCC others(248): Show |
G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-20240_-81-1998 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625680 | ||||||
| chr8:144625688
|
C | G | 94 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0065others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-81-19993G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625688 | ||||||
| chr8:144625702
|
C | T | 155 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(152): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-81-20007G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625702 | ||||||
| chr8:144625702
|
CCACTGCA others(197): Show |
C | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-81-20211_-81-2000 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625702 | ||||||
| chr8:144625720
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-20025C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625720 | ||||||
| chr8:144625731
|
C | G | 82 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(79): Show | 82 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-81-20036G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625731 | ||||||
| chr8:144625753
|
T | C | 78 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0027others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-81-20058A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625753 | ||||||
| chr8:144625766
|
C | T | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-81-20071G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625766 | ||||||
| chr8:144625782
|
G | C | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-20087C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625782 | ||||||
| chr8:144625790
|
CGTTCACG others(44): Show |
C | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-81-20146_-81-2009 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625790 | ||||||
| chr8:144625804
|
C | T | 168 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(165): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-81-20109G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625804 | ||||||
| chr8:144625822
|
G | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0238a0001c0001t0002g0241others(4): Show | 7 | HG02572.hp1 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-20127C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625822 | ||||||
| chr8:144625841
|
G | C | 12 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(9): Show | 12 | HG00558.hp2 HG01168.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-20146C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625841 | ||||||
| chr8:144625841
|
GGTTCACG others(197): Show |
G | 78 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-81-20350_-81-2014 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625841 | ||||||
| chr8:144625848
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-20153C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625848 | ||||||
| chr8:144625855
|
C | T | 3 | a0001c0002t0001g0020a0001c0002t0001g0133a0001c0007t0017g0019 | 3 | HG02647.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-81-20160G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625855 | ||||||
| chr8:144625873
|
T | G | 11 | a0001c0001t0001g0016a0001c0001t0003g0084a0001c0002t0001g0003others(8): Show | 11 | HG01346.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-20178A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625873 | ||||||
| chr8:144625876
|
CCTGTCCC others(199): Show |
C | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-81-20387_-81-2018 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625876 | ||||||
| chr8:144625884
|
G | C | 2 | a0001c0002t0001g0003a0001c0002t0001g0124 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-81-20189C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625884 | ||||||
| chr8:144625892
|
G | C | 10 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0002t0001g0003others(7): Show | 10 | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-20197C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625892 | ||||||
| chr8:144625906
|
T | C | 8 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(5): Show | 8 | HG00558.hp2 HG01168.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-20211A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625906 | ||||||
| chr8:144625934
|
C | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0124 | 2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-81-20239G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625934 | ||||||
| chr8:144625935
|
C | G | 7 | a0001c0001t0001g0016a0001c0001t0016g0105a0001c0002t0001g0003others(4): Show | 7 | HG01346.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-20240G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625935 | ||||||
| chr8:144625935
|
CGCGGCCC others(44): Show |
C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-20291_-81-2024 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625935 | ||||||
| chr8:144625936
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0221 | 2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-81-20241C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625936 | ||||||
| chr8:144625957
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0001t0018g0022others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-20262A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625957 | ||||||
| chr8:144625957
|
TCACTGCA others(44): Show |
T | 9 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-20313_-81-2026 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625957 | ||||||
| chr8:144625957
|
TCACTGCA others(401): Show |
T | 1 | a0001c0010t0001g0009 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-81-20670_-81-2026 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625957 | ||||||
| chr8:144625973
|
C | A | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-20278G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625973 | ||||||
| chr8:144625975
|
GCCCCTGT others(197): Show |
G | 2 | a0001c0001t0001g0211a0001c0002t0001g0098 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-81-20484_-81-2028 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625975 | ||||||
| chr8:144625986
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-20291C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625986 | ||||||
| chr8:144625988
|
CGGCCCCG others(350): Show |
C | 4 | a0001c0001t0001g0184a0001c0002t0001g0013a0001c0007t0003g0078others(1): Show | 4 | HG01361.hp2 HG02257.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-20650_-81-2029 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625988 | ||||||
| chr8:144625994
|
C | G | 12 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-20299G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144625994 | ||||||
| chr8:144626008
|
C | T | 83 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-81-20313G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626008 | ||||||
| chr8:144626026
|
G | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81-20331C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626026 | ||||||
| chr8:144626026
|
GCCCCTGT others(146): Show |
G | 75 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(72): Show | 75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.-81-20484_-81-2033 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626026 | ||||||
| chr8:144626037
|
G | C | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-20342C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626037 | ||||||
| chr8:144626039
|
CGGCCCCG others(299): Show |
C | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-20650_-81-2034 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626039 | ||||||
| chr8:144626045
|
C | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-81-20350G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626045 | ||||||
| chr8:144626045
|
C | G | 26 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0223others(23): Show | 26 | HG01346.hp2 HG02109.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.-81-20350G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626045 | ||||||
| chr8:144626059
|
C | T | 92 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-81-20364G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626059 | ||||||
| chr8:144626088
|
G | C | 83 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-81-20393C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626088 | ||||||
| chr8:144626088
|
G | T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-81-20393C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626088 | ||||||
| chr8:144626090
|
CGGCCCCG others(248): Show |
C | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-81-20650_-81-2039 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626090 | ||||||
| chr8:144626096
|
C | G | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-81-20401G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626096 | ||||||
| chr8:144626110
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0007t0001g0017 | 3 | HG02280.hp1 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-81-20415A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626110 | ||||||
| chr8:144626110
|
TCACTGCA others(248): Show |
T | 2 | a0001c0002t0001g0117a0001c0002t0001g0218 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-81-20670_-81-2041 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626110 | ||||||
| chr8:144626128
|
GCCCCTGT others(44): Show |
G | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-20484_-81-2043 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626128 | ||||||
| chr8:144626161
|
C | T | 84 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-81-20466G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626161 | ||||||
| chr8:144626179
|
T | G | 104 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0045others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-81-20484A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626179 | ||||||
| chr8:144626198
|
G | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-20503C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626198 | ||||||
| chr8:144626212
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-20517G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626212 | ||||||
| chr8:144626226
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(24): Show | 27 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.-81-20531C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626226 | ||||||
| chr8:144626230
|
T | G | 12 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0229others(9): Show | 12 | HG00558.hp2 HG02109.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-20535A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626230 | ||||||
| chr8:144626249
|
G | C | 13 | a0001c0001t0003g0023a0001c0001t0003g0068a0001c0001t0003g0071others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81-20554C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626249 | ||||||
| chr8:144626263
|
T | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-20568A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626263 | ||||||
| chr8:144626289
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-20594G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626289 | ||||||
| chr8:144626292
|
C | CGCGGCCC others(44): Show |
1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-20598_-81-2059 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626292 | ||||||
| chr8:144626292
|
C | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-20597G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626292 | ||||||
| chr8:144626314
|
T | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0238a0001c0001t0002g0241others(6): Show | 9 | HG00323.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-20619A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626314 | ||||||
| chr8:144626314
|
TCACTGCA others(44): Show |
T | 7 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0001t0003g0084others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-20670_-81-2062 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626314 | ||||||
| chr8:144626345
|
A | C | 197 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-81-20650T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626345 | ||||||
| chr8:144626351
|
C | G | 2 | a0001c0007t0001g0017a0001c0007t0003g0078 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-81-20656G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626351 | ||||||
| chr8:144626357
|
C | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-20662G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626357 | ||||||
| chr8:144626365
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0223others(15): Show | 18 | HG02109.hp1 HG02257.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-81-20670G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626365 | ||||||
| chr8:144626378
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-20683G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626378 | ||||||
| chr8:144626383
|
G | T | 6 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-20688C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626383 | ||||||
| chr8:144626402
|
C | G | 15 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-81-20707G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626402 | ||||||
| chr8:144626416
|
C | T | 6 | a0001c0001t0003g0084a0001c0002t0001g0021a0001c0002t0001g0082others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-20721G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626416 | ||||||
| chr8:144626416
|
CCACTGCA others(95): Show |
C | 16 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(13): Show | 16 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-81-20823_-81-2072 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626416 | ||||||
| chr8:144626434
|
G | T | 168 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-81-20739C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626434 | ||||||
| chr8:144626445
|
G | C | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-20750C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626445 | ||||||
| chr8:144626448
|
G | GGCCCGGT others(197): Show |
1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-20754_-81-2075 others(208): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626448 | ||||||
| chr8:144626453
|
C | G | 17 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(14): Show | 17 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-20758G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626453 | ||||||
| chr8:144626467
|
C | T | 12 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(9): Show | 12 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-20772G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626467 | ||||||
| chr8:144626467
|
CCACTGCA others(44): Show |
C | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-20823_-81-2077 others(55): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626467 | ||||||
| chr8:144626480
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-20785G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626480 | ||||||
| chr8:144626496
|
C | G | 15 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(12): Show | 15 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-81-20801G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626496 | ||||||
| chr8:144626504
|
C | G | 15 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(12): Show | 15 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-81-20809G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626504 | ||||||
| chr8:144626518
|
T | C | 21 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(18): Show | 21 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.-81-20823A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626518 | ||||||
| chr8:144626569
|
C | T | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-20874G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626569 | ||||||
| chr8:144626583
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-20888C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626583 | ||||||
| chr8:144626587
|
T | G | 176 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-81-20892A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626587 | ||||||
| chr8:144626606
|
C | G | 1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-81-20911G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626606 | ||||||
| chr8:144626758
|
G | A | 14 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(11): Show | 14 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81-21063C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626758 | ||||||
| chr8:144626828
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-81-21133G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626828 | ||||||
| chr8:144626974
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-81-21279C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144626974 | ||||||
| chr8:144627011
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81-21316G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627011 | ||||||
| chr8:144627057
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0002g0241 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-81-21362T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627057 | ||||||
| chr8:144627074
|
G | C | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-81-21379C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627074 | ||||||
| chr8:144627107
|
A | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-21412T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627107 | ||||||
| chr8:144627284
|
G | C | 176 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-81-21589C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627284 | ||||||
| chr8:144627391
|
A | G | 5 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-21696T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627391 | ||||||
| chr8:144627509
|
C | G | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-21814G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627509 | ||||||
| chr8:144627529
|
T | G | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81-21834A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627529 | ||||||
| chr8:144627554
|
C | CA | 31 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0049others(28): Show | 31 | HG00438.hp1 HG00558.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.-81-21860dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627554 | ||||||
| chr8:144627554
|
C | CAA | 86 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-81-21861_-81-2186 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627554 | ||||||
| chr8:144627554
|
C | CAAA | 76 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-81-21862_-81-2186 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627554 | ||||||
| chr8:144627554
|
CA | C | 11 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-21860delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627554 | ||||||
| chr8:144627665
|
G | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-81-21970C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627665 | ||||||
| chr8:144627820
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-81-22125G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627820 | ||||||
| chr8:144627950
|
G | C | 1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-81-22255C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627950 | ||||||
| chr8:144627999
|
T | C | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-81-22304A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144627999 | ||||||
| chr8:144628035
|
G | T | 1 | a0001c0001t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-81-22340C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628035 | ||||||
| chr8:144628407
|
G | A | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-22712C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628407 | ||||||
| chr8:144628655
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-81-22960G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628655 | ||||||
| chr8:144628866
|
C | A | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-81-23171G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628866 | ||||||
| chr8:144628867
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-23172C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628867 | ||||||
| chr8:144628972
|
C | T | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81-23277G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144628972 | ||||||
| chr8:144629017
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-23322G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629017 | ||||||
| chr8:144629062
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(1): Show | 4 | HG02976.hp2 HG03195.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-23367C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629062 | ||||||
| chr8:144629249
|
T | C | 77 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(74): Show |
intron_variant | MODIFIER | c.-81-23554A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629249 | ||||||
| chr8:144629255
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-23560G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629255 | ||||||
| chr8:144629403
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-23708G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629403 | ||||||
| chr8:144629431
|
C | G | 77 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(74): Show |
intron_variant | MODIFIER | c.-81-23736G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629431 | ||||||
| chr8:144629478
|
G | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-23783C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629478 | ||||||
| chr8:144629571
|
G | A | 1 | a0001c0002t0001g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-81-23876C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629571 | ||||||
| chr8:144629606
|
C | T | 55 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.-81-23911G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629606 | ||||||
| chr8:144629684
|
G | A | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-23989C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629684 | ||||||
| chr8:144629692
|
C | G | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-23997G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629692 | ||||||
| chr8:144629839
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-81-24144C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629839 | ||||||
| chr8:144629881
|
T | G | 1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-81-24186A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629881 | ||||||
| chr8:144629985
|
C | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.-81-24290G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144629985 | ||||||
| chr8:144630095
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-81-24400C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630095 | ||||||
| chr8:144630121
|
C | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.-81-24426G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630121 | ||||||
| chr8:144630186
|
C | G | 1 | a0001c0002t0001g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-81-24491G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630186 | ||||||
| chr8:144630200
|
T | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.-81-24505A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630200 | ||||||
| chr8:144630232
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0002g0123 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-81-24537A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630232 | ||||||
| chr8:144630235
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-81-24540A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630235 | ||||||
| chr8:144630413
|
G | A | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81-24718C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630413 | ||||||
| chr8:144630636
|
A | G | 197 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(194): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.-81-24941T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630636 | ||||||
| chr8:144630947
|
C | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.-81-25252G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630947 | ||||||
| chr8:144630948
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-81-25253C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630948 | ||||||
| chr8:144630991
|
G | C | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-25296C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144630991 | ||||||
| chr8:144631024
|
T | C | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-25329A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631024 | ||||||
| chr8:144631095
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-81-25400G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631095 | ||||||
| chr8:144631107
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-25412G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631107 | ||||||
| chr8:144631122
|
T | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-25427A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631122 | ||||||
| chr8:144631173
|
A | G | 1 | a0001c0001t0008g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-81-25478T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631173 | ||||||
| chr8:144631359
|
A | G | 55 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.-81-25664T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631359 | ||||||
| chr8:144631371
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-25676C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631371 | ||||||
| chr8:144631492
|
T | A | 1 | a0001c0002t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-81-25797A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631492 | ||||||
| chr8:144631500
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-81-25805G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631500 | ||||||
| chr8:144631524
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-81-25829G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631524 | ||||||
| chr8:144631868
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-81-26173C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144631868 | ||||||
| chr8:144632330
|
A | G | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-81-26635T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632330 | ||||||
| chr8:144632401
|
G | A | 81 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-81-26706C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632401 | ||||||
| chr8:144632513
|
C | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0098others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-81-26818G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632513 | ||||||
| chr8:144632693
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-81-26998G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632693 | ||||||
| chr8:144632711
|
C | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-81-27016G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632711 | ||||||
| chr8:144632784
|
A | G | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-27089T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632784 | ||||||
| chr8:144632914
|
C | G | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-27219G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632914 | ||||||
| chr8:144632937
|
C | G | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-27242G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144632937 | ||||||
| chr8:144633137
|
G | GT | 11 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-27443dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633137 | ||||||
| chr8:144633143
|
T | TTTTG | 12 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-27452_-81-2744 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633143 | ||||||
| chr8:144633147
|
G | T | 72 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(69): Show | 72 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(69): Show |
intron_variant | MODIFIER | c.-81-27452C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633147 | ||||||
| chr8:144633149
|
T | G | 4 | a0001c0002t0001g0035a0001c0002t0001g0051a0001c0007t0017g0019others(1): Show | 4 | HG02080.hp1 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-27454A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633149 | ||||||
| chr8:144633151
|
G | T | 53 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 53 | HG00408.hp1 HG00438.hp1 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81-27456C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633151 | ||||||
| chr8:144633152
|
T | G | 40 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(37): Show | 40 | HG00408.hp1 HG01192.hp2 HG02004.hp1 others(37): Show |
intron_variant | MODIFIER | c.-81-27457A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633152 | ||||||
| chr8:144633152
|
T | TG | 3 | a0001c0001t0001g0047a0001c0001t0003g0023a0001c0001t0014g0054 | 3 | HG00438.hp1 HG03209.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-81-27458_-81-2745 others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633152 | ||||||
| chr8:144633452
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-81-27757G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633452 | ||||||
| chr8:144633797
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-81-28102G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144633797 | ||||||
| chr8:144634001
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-81-28306C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634001 | ||||||
| chr8:144634102
|
G | GGGAACTC others(239): Show |
1 | a0001c0001t0002g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-81-28408_-81-2840 others(250): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634102 | ||||||
| chr8:144634121
|
T | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-28426A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634121 | ||||||
| chr8:144634121
|
TGGCGCAT others(34): Show |
T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-28467_-81-2842 others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634121 | ||||||
| chr8:144634121
|
TGGCGCAT others(198): Show |
T | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-28631_-81-2842 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634121 | ||||||
| chr8:144634125
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0194 | 2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-81-28430C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634125 | ||||||
| chr8:144634128
|
T | G | 243 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-81-28433A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634128 | ||||||
| chr8:144634139
|
A | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-28444T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634139 | ||||||
| chr8:144634144
|
A | AGAACTCC others(34): Show |
10 | a0001c0001t0003g0084a0001c0001t0008g0120a0001c0001t0008g0166others(7): Show | 10 | HG00323.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81-28490_-81-2845 others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
A | AGAACTCC others(75): Show |
1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-81-28531_-81-2845 others(86): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
A | AGAACTCC others(690): Show |
1 | a0001c0001t0008g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-81-29146_-81-2845 others(701): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
A | AGAACTCC others(239): Show |
1 | a0001c0001t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-81-28450_-81-2844 others(250): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
A | G | 3 | a0001c0001t0001g0207a0001c0002t0001g0015a0001c0007t0003g0078 | 3 | HG02257.hp1 HG03579.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-81-28449T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(34): Show |
A | 52 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0100others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-81-28490_-81-2845 others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(75): Show |
A | 9 | a0001c0001t0001g0060a0001c0001t0001g0148a0001c0001t0001g0149others(6): Show | 9 | HG00558.hp1 HG00735.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81-28531_-81-2845 others(86): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(116): Show |
A | 11 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0238others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81-28572_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(157): Show |
A | 33 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 33 | HG01192.hp2 HG02004.hp1 HG02080.hp1 others(30): Show |
intron_variant | MODIFIER | c.-81-28613_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(198): Show |
A | 10 | a0001c0001t0001g0016a0001c0001t0001g0184a0001c0001t0003g0063others(7): Show | 10 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-28654_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(239): Show |
A | 2 | a0001c0001t0001g0135a0001c0002t0009g0028 | 2 | HG03927.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-81-28695_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(280): Show |
A | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-28736_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(321): Show |
A | 3 | a0001c0001t0001g0077a0001c0001t0001g0211a0005c0013t0002g0195 | 3 | HG01496.hp2 HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-81-28777_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(362): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-81-28818_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634144
|
AGAACTCC others(485): Show |
A | 12 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0229others(9): Show | 12 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81-28941_-81-2845 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634144 | ||||||
| chr8:144634180
|
T | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-28485A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634180 | ||||||
| chr8:144634185
|
G | GGAACTCC others(157): Show |
1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-81-28491_-81-2849 others(168): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634185 | ||||||
| chr8:144634397
|
C | T | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81-28702G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144634397 | ||||||
| chr8:144635017
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-29322C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635017 | ||||||
| chr8:144635220
|
G | A | 5 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-29525C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635220 | ||||||
| chr8:144635254
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81-29559T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635254 | ||||||
| chr8:144635298
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-29603C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635298 | ||||||
| chr8:144635431
|
T | C | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-81-29736A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635431 | ||||||
| chr8:144635461
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-81-29766G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635461 | ||||||
| chr8:144635671
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-81-29976G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635671 | ||||||
| chr8:144635685
|
G | A | 27 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(24): Show | 27 | HG02004.hp1 HG02080.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.-81-29990C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635685 | ||||||
| chr8:144635735
|
GCTGAGGC others(63): Show |
G | 1 | a0001c0006t0001g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-81-30110_-81-3004 others(74): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635735 | ||||||
| chr8:144635805
|
T | TCTGAGGC others(41): Show |
3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-81-30158_-81-3011 others(52): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635805 | ||||||
| chr8:144635805
|
TCTGAGGC others(41): Show |
T | 41 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(38): Show | 41 | HG00438.hp1 HG01891.hp1 HG02004.hp1 others(38): Show |
intron_variant | MODIFIER | c.-81-30158_-81-3011 others(52): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635805 | ||||||
| chr8:144635805
|
TCTGAGGC others(89): Show |
T | 57 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0100others(54): Show | 57 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-81-30206_-81-3011 others(100): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635805 | ||||||
| chr8:144635816
|
C | CGCCAGGT others(41): Show |
1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-81-30122_-81-3012 others(52): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635816 | ||||||
| chr8:144635853
|
G | GCTGAGGC others(63): Show |
1 | a0001c0002t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-81-30159_-81-3015 others(74): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635853 | ||||||
| chr8:144635912
|
C | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(30): Show | 33 | HG00438.hp1 HG02004.hp1 HG02080.hp1 others(30): Show |
intron_variant | MODIFIER | c.-81-30217G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635912 | ||||||
| chr8:144635955
|
G | A | 4 | a0001c0002t0001g0106a0001c0002t0001g0111a0001c0002t0001g0112others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-30260C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144635955 | ||||||
| chr8:144636231
|
T | C | 1 | a0001c0003t0001g0005 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-81-30536A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636231 | ||||||
| chr8:144636501
|
G | A | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-30806C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636501 | ||||||
| chr8:144636587
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-30892G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636587 | ||||||
| chr8:144636720
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-81-31025C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636720 | ||||||
| chr8:144636820
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-81-31125C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636820 | ||||||
| chr8:144636925
|
T | A | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-31230A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144636925 | ||||||
| chr8:144637349
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-31654G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637349 | ||||||
| chr8:144637515
|
C | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-81-31820G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637515 | ||||||
| chr8:144637713
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-81-32018A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637713 | ||||||
| chr8:144637822
|
G | A | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-32127C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637822 | ||||||
| chr8:144637828
|
T | C | 64 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(61): Show |
intron_variant | MODIFIER | c.-81-32133A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637828 | ||||||
| chr8:144637864
|
C | CT | 46 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0031others(43): Show | 46 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.-81-32170dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637864 | ||||||
| chr8:144637939
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-32244G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144637939 | ||||||
| chr8:144638120
|
A | T | 4 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81-32425T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638120 | ||||||
| chr8:144638163
|
T | C | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-32468A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638163 | ||||||
| chr8:144638229
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-81-32534C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638229 | ||||||
| chr8:144638254
|
C | T | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-81-32559G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638254 | ||||||
| chr8:144638286
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG00558.hp1 NA18997.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81-32591A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638286 | ||||||
| chr8:144638341
|
C | T | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-32646G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638341 | ||||||
| chr8:144638374
|
T | C | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0147 | 3 | HG00735.hp1 HG01981.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-81-32679A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638374 | ||||||
| chr8:144638528
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(63): Show | 66 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(63): Show |
intron_variant | MODIFIER | c.-81-32833G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638528 | ||||||
| chr8:144638546
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-81-32851C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638546 | ||||||
| chr8:144638678
|
CTT | C | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-32985_-81-3298 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638678 | ||||||
| chr8:144638835
|
T | C | 12 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81-33140A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638835 | ||||||
| chr8:144638929
|
A | G | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-81-33234T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638929 | ||||||
| chr8:144638936
|
T | C | 1 | a0002c0008t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-81-33241A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144638936 | ||||||
| chr8:144639081
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-81-33386G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639081 | ||||||
| chr8:144639081
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-81-33386G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639081 | ||||||
| chr8:144639092
|
C | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0170a0001c0002t0001g0140 | 3 | HG02280.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-81-33397G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639092 | ||||||
| chr8:144639183
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81-33488G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639183 | ||||||
| chr8:144639211
|
C | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-81-33516G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639211 | ||||||
| chr8:144639251
|
G | A | 1 | a0001c0001t0007g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81-33556C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639251 | ||||||
| chr8:144639265
|
G | A | 6 | a0001c0002t0001g0013a0001c0005t0001g0006a0001c0005t0001g0010others(3): Show | 6 | HG00639.hp1 HG01168.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-33570C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639265 | ||||||
| chr8:144639281
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-81-33586C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639281 | ||||||
| chr8:144639325
|
C | CA | 14 | a0001c0001t0001g0030a0001c0001t0001g0196a0001c0001t0002g0131others(11): Show | 14 | HG01192.hp2 HG01358.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-33631dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639325 | ||||||
| chr8:144639325
|
CAAAA | C | 5 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-33634_-81-3363 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639325 | ||||||
| chr8:144639338
|
A | AAAAG | 7 | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0004t0006g0069others(4): Show | 7 | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-33647_-81-3364 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639338 | ||||||
| chr8:144639338
|
A | G | 14 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(11): Show | 14 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81-33643T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639338 | ||||||
| chr8:144639338
|
AAAAG | A | 17 | a0001c0001t0001g0061a0001c0001t0001g0151a0001c0001t0001g0219others(14): Show | 17 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.-81-33647_-81-3364 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639338 | ||||||
| chr8:144639342
|
G | A | 33 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(30): Show | 33 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.-81-33647C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144639342 | ||||||
| chr8:144640132
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-81-34437C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640132 | ||||||
| chr8:144640359
|
G | T | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085 | 3 | HG02258.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-81-34664C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640359 | ||||||
| chr8:144640401
|
C | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-34706G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640401 | ||||||
| chr8:144640628
|
C | G | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-81-34933G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640628 | ||||||
| chr8:144640716
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-35021G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640716 | ||||||
| chr8:144640760
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-35065G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640760 | ||||||
| chr8:144640825
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-81-35130A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640825 | ||||||
| chr8:144640842
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-81-35147C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144640842 | ||||||
| chr8:144641185
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-35490G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641185 | ||||||
| chr8:144641189
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-35494C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641189 | ||||||
| chr8:144641218
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-81-35523T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641218 | ||||||
| chr8:144641238
|
C | G | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81-35543G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641238 | ||||||
| chr8:144641295
|
A | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-35600T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641295 | ||||||
| chr8:144641385
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-81-35690G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641385 | ||||||
| chr8:144641430
|
C | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.-81-35735G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641430 | ||||||
| chr8:144641452
|
G | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(61): Show |
intron_variant | MODIFIER | c.-81-35757C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641452 | ||||||
| chr8:144641552
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81-35857G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641552 | ||||||
| chr8:144641698
|
G | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(61): Show |
intron_variant | MODIFIER | c.-81-36003C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641698 | ||||||
| chr8:144641820
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81-36125T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641820 | ||||||
| chr8:144641833
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-36138C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144641833 | ||||||
| chr8:144642032
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-81-36337C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642032 | ||||||
| chr8:144642419
|
G | A | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-36724C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642419 | ||||||
| chr8:144642468
|
C | T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-81-36773G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642468 | ||||||
| chr8:144642481
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-81-36786G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642481 | ||||||
| chr8:144642487
|
A | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-81-36792T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642487 | ||||||
| chr8:144642511
|
T | TA | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0107others(4): Show | 7 | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-36817dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642511 | ||||||
| chr8:144642511
|
TA | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0197others(3): Show | 6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81-36817delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642511 | ||||||
| chr8:144642539
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-36844G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642539 | ||||||
| chr8:144642613
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81-36918C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642613 | ||||||
| chr8:144642773
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-81-37078G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642773 | ||||||
| chr8:144642864
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0227 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-81-37169A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642864 | ||||||
| chr8:144642957
|
G | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81-37262C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642957 | ||||||
| chr8:144642973
|
A | G | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-37278T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144642973 | ||||||
| chr8:144643037
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-81-37342T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643037 | ||||||
| chr8:144643038
|
T | C | 42 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-81-37343A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643038 | ||||||
| chr8:144643043
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-81-37348T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643043 | ||||||
| chr8:144643173
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-37478C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643173 | ||||||
| chr8:144643544
|
A | G | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-81-37849T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643544 | ||||||
| chr8:144643697
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-81-38002T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643697 | ||||||
| chr8:144643823
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-81-38128A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144643823 | ||||||
| chr8:144644143
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-81-38448C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644143 | ||||||
| chr8:144644305
|
G | A | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-38610C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644305 | ||||||
| chr8:144644378
|
C | T | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-81-38683G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644378 | ||||||
| chr8:144644393
|
C | T | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81-38698G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644393 | ||||||
| chr8:144644394
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81-38699C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644394 | ||||||
| chr8:144644599
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81-38904G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644599 | ||||||
| chr8:144644641
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-81-38946C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644641 | ||||||
| chr8:144644712
|
G | C | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-81-39017C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644712 | ||||||
| chr8:144644741
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-81-39046C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644741 | ||||||
| chr8:144644781
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81-39086C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644781 | ||||||
| chr8:144644796
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0194 | 2 | HG01099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-81-39101A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644796 | ||||||
| chr8:144644981
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-81-39286C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144644981 | ||||||
| chr8:144645053
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81-39358C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144645053 | ||||||
| chr8:144645071
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-81-39376G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144645071 | ||||||
| chr8:144645630
|
G | A | 1 | a0001c0001t0004g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-81-39935C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144645630 | ||||||
| chr8:144645715
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0002g0241 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-82+39971A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144645715 | ||||||
| chr8:144645773
|
C | T | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-82+39913G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144645773 | ||||||
| chr8:144646049
|
G | T | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+39637C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646049 | ||||||
| chr8:144646073
|
G | A | 1 | a0001c0004t0006g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-82+39613C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646073 | ||||||
| chr8:144646297
|
C | A | 1 | a0001c0002t0001g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-82+39389G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646297 | ||||||
| chr8:144646307
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-82+39379C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646307 | ||||||
| chr8:144646356
|
G | A | 6 | a0001c0001t0002g0134a0001c0001t0002g0139a0001c0001t0002g0145others(3): Show | 6 | HG02280.hp2 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+39330C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646356 | ||||||
| chr8:144646379
|
G | A | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-82+39307C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646379 | ||||||
| chr8:144646401
|
CTGTT | C | 4 | a0001c0001t0001g0184a0001c0002t0001g0087a0001c0002t0001g0088others(1): Show | 4 | HG00639.hp2 HG02683.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+39281_-82+3928 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646401 | ||||||
| chr8:144646525
|
C | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(27): Show |
intron_variant | MODIFIER | c.-82+39161G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646525 | ||||||
| chr8:144646571
|
G | A | 1 | a0003c0011t0001g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-82+39115C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646571 | ||||||
| chr8:144646795
|
C | T | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+38891G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646795 | ||||||
| chr8:144646848
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+38838G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646848 | ||||||
| chr8:144646965
|
A | AT | 57 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0031others(54): Show | 57 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-82+38720dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646965 | ||||||
| chr8:144646965
|
A | ATT | 11 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0036others(8): Show | 11 | HG00408.hp2 HG00438.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-82+38719_-82+3872 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646965 | ||||||
| chr8:144646965
|
A | T | 7 | a0001c0001t0001g0209a0001c0001t0001g0221a0001c0001t0003g0063others(4): Show | 7 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-82+38721T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646965 | ||||||
| chr8:144646965
|
AT | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0202a0001c0001t0002g0235others(2): Show | 5 | HG01074.hp2 HG01169.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+38720delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144646965 | ||||||
| chr8:144647031
|
C | T | 1 | a0001c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-82+38655G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647031 | ||||||
| chr8:144647054
|
C | T | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+38632G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647054 | ||||||
| chr8:144647113
|
C | A | 2 | a0002c0008t0001g0067a0002c0008t0001g0142 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-82+38573G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647113 | ||||||
| chr8:144647297
|
T | A | 1 | a0001c0001t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-82+38389A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647297 | ||||||
| chr8:144647324
|
G | A | 6 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0005g0187others(3): Show | 6 | HG00323.hp2 HG00735.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82+38362C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647324 | ||||||
| chr8:144647390
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-82+38296G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647390 | ||||||
| chr8:144647419
|
C | T | 12 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-82+38267G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647419 | ||||||
| chr8:144647491
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-82+38195G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647491 | ||||||
| chr8:144647505
|
C | T | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+38181G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647505 | ||||||
| chr8:144647634
|
C | T | 1 | a0001c0001t0021g0062 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-82+38052G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647634 | ||||||
| chr8:144647745
|
G | C | 8 | a0001c0001t0002g0131a0001c0001t0007g0168a0001c0002t0001g0126others(5): Show | 8 | HG01192.hp2 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+37941C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144647745 | ||||||
| chr8:144648041
|
A | G | 1 | a0001c0002t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-82+37645T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648041 | ||||||
| chr8:144648131
|
T | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+37555A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648131 | ||||||
| chr8:144648189
|
A | G | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-82+37497T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648189 | ||||||
| chr8:144648356
|
C | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+37330G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648356 | ||||||
| chr8:144648426
|
T | C | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-82+37260A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648426 | ||||||
| chr8:144648477
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+37209G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648477 | ||||||
| chr8:144648486
|
G | C | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+37200C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648486 | ||||||
| chr8:144648506
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-82+37180C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648506 | ||||||
| chr8:144648655
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+37031G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648655 | ||||||
| chr8:144648690
|
C | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+36996G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648690 | ||||||
| chr8:144648774
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+36912G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648774 | ||||||
| chr8:144648900
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+36786A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648900 | ||||||
| chr8:144648937
|
G | A | 17 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(14): Show | 17 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+36749C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648937 | ||||||
| chr8:144648974
|
C | G | 1 | a0001c0007t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-82+36712G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144648974 | ||||||
| chr8:144649133
|
G | T | 1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-82+36553C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649133 | ||||||
| chr8:144649172
|
G | A | 2 | a0001c0001t0001g0122a0002c0008t0001g0142 | 2 | HG00558.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-82+36514C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649172 | ||||||
| chr8:144649319
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+36367C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649319 | ||||||
| chr8:144649341
|
T | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+36345A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649341 | ||||||
| chr8:144649363
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-82+36323A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649363 | ||||||
| chr8:144649445
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-82+36241C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649445 | ||||||
| chr8:144649721
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-82+35965T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649721 | ||||||
| chr8:144649827
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-82+35859G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649827 | ||||||
| chr8:144649900
|
T | C | 1 | a0001c0002t0001g0140 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-82+35786A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649900 | ||||||
| chr8:144649965
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+35721T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144649965 | ||||||
| chr8:144650016
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-82+35670C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650016 | ||||||
| chr8:144650061
|
T | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+35625A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650061 | ||||||
| chr8:144650143
|
GGAAAAAA others(3): Show |
G | 1 | a0001c0001t0002g0170 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-82+35533_-82+3554 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650143 | ||||||
| chr8:144650198
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+35488G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650198 | ||||||
| chr8:144650563
|
A | C | 1 | a0001c0002t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-82+35123T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650563 | ||||||
| chr8:144650960
|
C | T | 1 | a0001c0002t0022g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-82+34726G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650960 | ||||||
| chr8:144650973
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+34713A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144650973 | ||||||
| chr8:144651541
|
A | G | 3 | a0001c0004t0006g0073a0001c0004t0006g0074a0001c0004t0006g0075 | 3 | HG02886.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-82+34145T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144651541 | ||||||
| chr8:144651577
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-82+34109G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144651577 | ||||||
| chr8:144651958
|
C | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+33728G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144651958 | ||||||
| chr8:144652009
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+33677A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652009 | ||||||
| chr8:144652048
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+33638G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652048 | ||||||
| chr8:144652198
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-82+33488C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652198 | ||||||
| chr8:144652202
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+33484C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652202 | ||||||
| chr8:144652472
|
C | A | 1 | a0001c0001t0005g0189 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-82+33214G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652472 | ||||||
| chr8:144652858
|
C | G | 1 | a0001c0001t0004g0152 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-82+32828G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144652858 | ||||||
| chr8:144653215
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-82+32471G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653215 | ||||||
| chr8:144653537
|
G | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+32149C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653537 | ||||||
| chr8:144653597
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+32089C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653597 | ||||||
| chr8:144653687
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-82+31999C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653687 | ||||||
| chr8:144653691
|
G | GGGTCATG others(55): Show |
34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+31933_-82+3199 others(66): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653691 | ||||||
| chr8:144653848
|
T | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 8 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-82+31838A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653848 | ||||||
| chr8:144653975
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+31711C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653975 | ||||||
| chr8:144653996
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+31690C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144653996 | ||||||
| chr8:144654176
|
A | G | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+31510T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654176 | ||||||
| chr8:144654498
|
T | C | 55 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(52): Show | 55 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-82+31188A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654498 | ||||||
| chr8:144654545
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-82+31141C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654545 | ||||||
| chr8:144654636
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-82+31050C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654636 | ||||||
| chr8:144654794
|
G | C | 1 | a0001c0001t0002g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-82+30892C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654794 | ||||||
| chr8:144654875
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+30811C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144654875 | ||||||
| chr8:144655428
|
GCCCAATC others(7252): Show |
G | 1 | a0001c0001t0007g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-82+22999_-82+3025 others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655428 | ||||||
| chr8:144655513
|
T | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-82+30173A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655513 | ||||||
| chr8:144655751
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-82+29935A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655751 | ||||||
| chr8:144655776
|
G | A | 1 | a0004c0009t0001g0008 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-82+29910C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655776 | ||||||
| chr8:144655811
|
C | T | 51 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0100others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-82+29875G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655811 | ||||||
| chr8:144655813
|
C | T | 8 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+29873G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655813 | ||||||
| chr8:144655912
|
C | A | 1 | a0001c0002t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-82+29774G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655912 | ||||||
| chr8:144655924
|
C | T | 1 | a0001c0005t0001g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-82+29762G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655924 | ||||||
| chr8:144655948
|
C | T | 81 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-82+29738G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655948 | ||||||
| chr8:144655985
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-82+29701T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144655985 | ||||||
| chr8:144656194
|
GA | G | 60 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(57): Show |
intron_variant | MODIFIER | c.-82+29491delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656194 | ||||||
| chr8:144656194
|
GAA | G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+29490_-82+2949 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656194 | ||||||
| chr8:144656280
|
C | T | 4 | a0001c0001t0002g0139a0001c0001t0002g0145a0001c0001t0002g0170others(1): Show | 4 | HG02280.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82+29406G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656280 | ||||||
| chr8:144656464
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+29222T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656464 | ||||||
| chr8:144656528
|
C | G | 1 | a0001c0001t0005g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-82+29158G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656528 | ||||||
| chr8:144656577
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-82+29109G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656577 | ||||||
| chr8:144656632
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-82+29054G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656632 | ||||||
| chr8:144656778
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+28908T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656778 | ||||||
| chr8:144656807
|
C | CA | 55 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.-82+28878dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656807
|
C | CAA | 28 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0061others(25): Show | 28 | HG00408.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-82+28877_-82+2887 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656807
|
C | CAAA | 27 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0136others(24): Show | 27 | HG00323.hp1 HG00558.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-82+28876_-82+2887 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656807
|
C | CAAAA | 40 | a0001c0001t0001g0065a0001c0001t0001g0100a0001c0001t0001g0135others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-82+28875_-82+2887 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656807
|
C | CAAAAA | 8 | a0001c0002t0001g0003a0001c0002t0001g0066a0001c0002t0001g0104others(5): Show | 8 | HG00609.hp1 HG01074.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.-82+28874_-82+2887 others(9): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656807
|
CA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0003g0063others(3): Show | 6 | HG00323.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82+28878delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656807 | ||||||
| chr8:144656844
|
C | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(60): Show |
intron_variant | MODIFIER | c.-82+28842G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144656844 | ||||||
| chr8:144657136
|
G | A | 3 | a0001c0002t0001g0095a0001c0002t0001g0096a0001c0002t0001g0161 | 3 | HG02027.hp1 NA18979.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-82+28550C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657136 | ||||||
| chr8:144657157
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+28529C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657157 | ||||||
| chr8:144657262
|
A | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+28424T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657262 | ||||||
| chr8:144657459
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-82+28227C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657459 | ||||||
| chr8:144657555
|
C | G | 1 | a0001c0002t0019g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-82+28131G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657555 | ||||||
| chr8:144657591
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-82+28095T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657591 | ||||||
| chr8:144657731
|
T | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+27955A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657731 | ||||||
| chr8:144657770
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-82+27916G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657770 | ||||||
| chr8:144657824
|
T | C | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-82+27862A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657824 | ||||||
| chr8:144657942
|
TA | T | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+27743delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657942 | ||||||
| chr8:144657979
|
A | T | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-82+27707T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657979 | ||||||
| chr8:144657988
|
T | C | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-82+27698A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657988 | ||||||
| chr8:144657991
|
G | A | 1 | a0001c0001t0016g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-82+27695C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144657991 | ||||||
| chr8:144658077
|
T | C | 1 | a0001c0006t0001g0171 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-82+27609A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658077 | ||||||
| chr8:144658132
|
A | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(60): Show |
intron_variant | MODIFIER | c.-82+27554T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658132 | ||||||
| chr8:144658147
|
T | G | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-82+27539A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658147 | ||||||
| chr8:144658227
|
A | C | 2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-82+27459T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658227 | ||||||
| chr8:144658271
|
G | A | 5 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+27415C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658271 | ||||||
| chr8:144658276
|
A | AT | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-82+27409dupA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658276 | ||||||
| chr8:144658337
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+27349G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658337 | ||||||
| chr8:144658415
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-82+27271G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658415 | ||||||
| chr8:144658425
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-82+27261G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658425 | ||||||
| chr8:144658497
|
G | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(60): Show |
intron_variant | MODIFIER | c.-82+27189C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658497 | ||||||
| chr8:144658521
|
C | T | 1 | a0001c0005t0010g0001 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-82+27165G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658521 | ||||||
| chr8:144658566
|
C | T | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+27120G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144658566 | ||||||
| chr8:144659406
|
G | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+26280C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144659406 | ||||||
| chr8:144659588
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+26098A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144659588 | ||||||
| chr8:144659600
|
C | G | 12 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-82+26086G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144659600 | ||||||
| chr8:144659757
|
A | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+25929T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144659757 | ||||||
| chr8:144659757
|
A | G | 34 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(31): Show | 34 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+25929T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144659757 | ||||||
| chr8:144660028
|
C | T | 1 | a0001c0010t0001g0009 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-82+25658G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660028 | ||||||
| chr8:144660077
|
T | G | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+25609A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660077 | ||||||
| chr8:144660114
|
C | T | 1 | a0001c0014t0007g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-82+25572G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660114 | ||||||
| chr8:144660227
|
T | C | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-82+25459A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660227 | ||||||
| chr8:144660357
|
C | T | 1 | a0001c0002t0001g0164 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-82+25329G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660357 | ||||||
| chr8:144660408
|
G | A | 24 | a0001c0001t0001g0107a0001c0001t0001g0244a0001c0001t0001g0245others(21): Show | 24 | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.-82+25278C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660408 | ||||||
| chr8:144660462
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-82+25224G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660462 | ||||||
| chr8:144660516
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+25170C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660516 | ||||||
| chr8:144660798
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+24888C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660798 | ||||||
| chr8:144660848
|
G | C | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+24838C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660848 | ||||||
| chr8:144660876
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-82+24810G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660876 | ||||||
| chr8:144660900
|
C | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+24786G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660900 | ||||||
| chr8:144660948
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+24738C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144660948 | ||||||
| chr8:144661042
|
G | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+24644C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661042 | ||||||
| chr8:144661138
|
C | T | 10 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0196others(7): Show | 10 | HG01071.hp2 HG01358.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-82+24548G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661138 | ||||||
| chr8:144661210
|
AGAGGAGG others(20): Show |
A | 1 | a0001c0004t0006g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-82+24449_-82+2447 others(31): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661210 | ||||||
| chr8:144661239
|
A | T | 1 | a0001c0001t0002g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-82+24447T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661239 | ||||||
| chr8:144661306
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-82+24380G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661306 | ||||||
| chr8:144661320
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+24366C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661320 | ||||||
| chr8:144661480
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-82+24206G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661480 | ||||||
| chr8:144661497
|
G | A | 12 | a0001c0002t0001g0007a0001c0002t0001g0013a0001c0003t0001g0005others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-82+24189C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661497 | ||||||
| chr8:144661633
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-82+24053C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661633 | ||||||
| chr8:144661908
|
C | G | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-82+23778G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661908 | ||||||
| chr8:144661921
|
C | G | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+23765G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144661921 | ||||||
| chr8:144662216
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-82+23470C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662216 | ||||||
| chr8:144662284
|
C | T | 11 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(8): Show | 11 | HG00558.hp2 HG00609.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.-82+23402G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662284 | ||||||
| chr8:144662317
|
C | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+23369G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662317 | ||||||
| chr8:144662441
|
A | AC | 27 | a0001c0001t0001g0030a0001c0001t0001g0196a0001c0001t0001g0211others(24): Show | 27 | HG00438.hp2 HG01175.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.-82+23244dupG | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662441 | ||||||
| chr8:144662503
|
C | T | 5 | a0001c0001t0001g0163a0001c0002t0001g0092a0001c0002t0001g0093others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+23183G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662503 | ||||||
| chr8:144662562
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-82+23124G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662562 | ||||||
| chr8:144662615
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0117others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+23071G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662615 | ||||||
| chr8:144662721
|
C | T | 1 | a0001c0002t0001g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-82+22965G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662721 | ||||||
| chr8:144662840
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+22846G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662840 | ||||||
| chr8:144662989
|
T | C | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+22697A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144662989 | ||||||
| chr8:144663251
|
T | A | 1 | a0001c0002t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-82+22435A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663251 | ||||||
| chr8:144663252
|
A | T | 18 | a0001c0001t0001g0024a0001c0001t0001g0207a0001c0001t0001g0223others(15): Show | 18 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-82+22434T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663252 | ||||||
| chr8:144663260
|
G | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+22426C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663260 | ||||||
| chr8:144663345
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0221 | 2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-82+22341A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663345 | ||||||
| chr8:144663361
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-82+22325A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663361 | ||||||
| chr8:144663495
|
C | A | 3 | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-82+22191G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663495 | ||||||
| chr8:144663543
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0002t0001g0020others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+22143G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663543 | ||||||
| chr8:144663553
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+22133G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663553 | ||||||
| chr8:144663587
|
C | T | 1 | a0004c0009t0001g0008 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-82+22099G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663587 | ||||||
| chr8:144663714
|
G | A | 42 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(39): Show | 42 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-82+21972C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663714 | ||||||
| chr8:144663727
|
G | A | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+21959C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663727 | ||||||
| chr8:144663881
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-82+21805C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663881 | ||||||
| chr8:144663999
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-82+21687C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144663999 | ||||||
| chr8:144664168
|
C | T | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82+21518G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144664168 | ||||||
| chr8:144664612
|
G | A | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+21074C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144664612 | ||||||
| chr8:144664710
|
C | T | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-82+20976G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144664710 | ||||||
| chr8:144664718
|
TCTTC | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+20964_-82+2096 others(8): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144664718 | ||||||
| chr8:144664920
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+20766G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144664920 | ||||||
| chr8:144665025
|
G | A | 37 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(34): Show | 37 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.-82+20661C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665025 | ||||||
| chr8:144665037
|
T | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+20649A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665037 | ||||||
| chr8:144665087
|
A | G | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+20599T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665087 | ||||||
| chr8:144665420
|
C | T | 47 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.-82+20266G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665420 | ||||||
| chr8:144665448
|
G | A | 1 | a0001c0007t0001g0017 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-82+20238C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665448 | ||||||
| chr8:144665463
|
A | AGACCTTC others(8): Show |
1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+20208_-82+2022 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665463 | ||||||
| chr8:144665539
|
G | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+20147C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665539 | ||||||
| chr8:144665551
|
A | G | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+20135T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665551 | ||||||
| chr8:144665917
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0002g0241 | 2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-82+19769A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665917 | ||||||
| chr8:144665939
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-82+19747G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144665939 | ||||||
| chr8:144666086
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+19600C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666086 | ||||||
| chr8:144666136
|
T | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+19550A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666136 | ||||||
| chr8:144666155
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+19531C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666155 | ||||||
| chr8:144666382
|
G | T | 1 | a0001c0002t0001g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-82+19304C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666382 | ||||||
| chr8:144666399
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+19287C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666399 | ||||||
| chr8:144666459
|
T | A | 1 | a0001c0002t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-82+19227A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666459 | ||||||
| chr8:144666518
|
C | T | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+19168G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666518 | ||||||
| chr8:144666519
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-82+19167C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666519 | ||||||
| chr8:144666594
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0002t0001g0020others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+19092C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666594 | ||||||
| chr8:144666637
|
G | A | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG01074.hp2 HG01167.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82+19049C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666637 | ||||||
| chr8:144666723
|
T | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0232 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-82+18963A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666723 | ||||||
| chr8:144666769
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+18917G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666769 | ||||||
| chr8:144666858
|
G | A | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+18828C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144666858 | ||||||
| chr8:144667000
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+18686G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667000 | ||||||
| chr8:144667180
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-82+18506G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667180 | ||||||
| chr8:144667214
|
T | C | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+18472A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667214 | ||||||
| chr8:144667429
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-82+18257C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667429 | ||||||
| chr8:144667472
|
G | C | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+18214C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667472 | ||||||
| chr8:144667488
|
G | A | 3 | a0001c0001t0004g0237a0001c0001t0007g0239a0001c0014t0007g0240 | 3 | HG02572.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-82+18198C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667488 | ||||||
| chr8:144667577
|
C | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+18109G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667577 | ||||||
| chr8:144667782
|
G | A | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+17904C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667782 | ||||||
| chr8:144667787
|
C | T | 1 | a0001c0003t0001g0012 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-82+17899G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667787 | ||||||
| chr8:144667792
|
C | T | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+17894G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144667792 | ||||||
| chr8:144668020
|
CT | C | 70 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(67): Show | 70 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-82+17665delA | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668020 | ||||||
| chr8:144668051
|
A | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+17635T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668051 | ||||||
| chr8:144668154
|
T | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+17532A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668154 | ||||||
| chr8:144668220
|
C | G | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+17466G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668220 | ||||||
| chr8:144668427
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0117others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+17259C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668427 | ||||||
| chr8:144668607
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-82+17079C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668607 | ||||||
| chr8:144668751
|
T | G | 3 | a0001c0001t0001g0132a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01981.hp2 NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-82+16935A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144668751 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0007t0003g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(975): Show |
1 | a0001c0002t0001g0007 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(986): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(975): Show |
11 | a0001c0001t0001g0233a0001c0001t0003g0063a0001c0001t0003g0068others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(986): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(975): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0191a0001c0002t0001g0081others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(986): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG00558.hp1 NA18940.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
11 | a0001c0002t0001g0013a0001c0003t0001g0005a0001c0003t0001g0012others(8): Show | 11 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0001t0013g0192 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(977): Show |
1 | a0001c0006t0001g0193 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(988): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0047others(1): Show | 4 | NA18945.hp1 NA18999.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
44 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(41): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
149 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0065others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(974): Show |
2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(985): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669258
|
A | ACACTTTG others(976): Show |
1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-82+16427_-82+1642 others(987): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669258 | ||||||
| chr8:144669395
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0056 | 3 | HG02004.hp1 HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-82+16291A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669395 | ||||||
| chr8:144669501
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+16185C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669501 | ||||||
| chr8:144669506
|
C | CAA | 7 | a0001c0001t0001g0238a0001c0001t0002g0234a0001c0001t0002g0241others(4): Show | 7 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-82+16178_-82+1617 others(6): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAA | 15 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(12): Show | 15 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-82+16177_-82+1617 others(7): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(3): Show |
25 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(22): Show | 25 | HG00408.hp1 HG02004.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.-82+16170_-82+1617 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0014g0054 | 3 | HG00438.hp1 HG02135.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-82+16169_-82+1617 others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0049 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-82+16168_-82+1617 others(16): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-82+16166_-82+1617 others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0076 | 3 | HG01891.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-82+16165_-82+1617 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(9): Show |
4 | a0001c0004t0006g0069a0001c0004t0006g0073a0001c0004t0006g0074others(1): Show | 4 | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+16164_-82+1617 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0003g0071a0001c0004t0006g0070 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-82+16163_-82+1617 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0021g0062a0003c0011t0001g0072 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-82+16162_-82+1617 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669506
|
CA | C | 168 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-82+16179delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669506 | ||||||
| chr8:144669630
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+16056G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669630 | ||||||
| chr8:144669925
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+15761C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669925 | ||||||
| chr8:144669953
|
T | C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+15733A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144669953 | ||||||
| chr8:144670167
|
G | T | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+15519C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670167 | ||||||
| chr8:144670484
|
C | T | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-82+15202G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670484 | ||||||
| chr8:144670590
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+15096G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670590 | ||||||
| chr8:144670735
|
G | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+14951C>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670735 | ||||||
| chr8:144670808
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-82+14878A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670808 | ||||||
| chr8:144670816
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+14870A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144670816 | ||||||
| chr8:144671319
|
C | T | 1 | a0001c0002t0001g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-82+14367G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671319 | ||||||
| chr8:144671455
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-82+14231A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671455 | ||||||
| chr8:144671645
|
C | T | 1 | a0001c0016t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-82+14041G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671645 | ||||||
| chr8:144671681
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+14005G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671681 | ||||||
| chr8:144671705
|
G | A | 1 | a0005c0013t0002g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-82+13981C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671705 | ||||||
| chr8:144671780
|
C | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-82+13906G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671780 | ||||||
| chr8:144671959
|
G | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+13727C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144671959 | ||||||
| chr8:144672122
|
T | G | 1 | a0001c0001t0002g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-82+13564A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672122 | ||||||
| chr8:144672144
|
A | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+13542T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672144 | ||||||
| chr8:144672285
|
A | C | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+13401T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672285 | ||||||
| chr8:144672291
|
T | C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+13395A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672291 | ||||||
| chr8:144672336
|
G | A | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+13350C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672336 | ||||||
| chr8:144672377
|
C | T | 1 | a0001c0002t0001g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-82+13309G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672377 | ||||||
| chr8:144672405
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-82+13281G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672405 | ||||||
| chr8:144672520
|
G | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+13166C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672520 | ||||||
| chr8:144672545
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-82+13141G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672545 | ||||||
| chr8:144672873
|
C | G | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+12813G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672873 | ||||||
| chr8:144672988
|
G | A | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+12698C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144672988 | ||||||
| chr8:144673012
|
TTCAAAAC others(3): Show |
T | 1 | a0001c0012t0002g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-82+12664_-82+1267 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673012 | ||||||
| chr8:144673131
|
C | T | 4 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088others(1): Show | 4 | HG00639.hp2 HG02683.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82+12555G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673131 | ||||||
| chr8:144673132
|
G | A | 10 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0196others(7): Show | 10 | HG01071.hp2 HG01358.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-82+12554C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673132 | ||||||
| chr8:144673190
|
C | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+12496G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673190 | ||||||
| chr8:144673216
|
C | CAAAAAAA | 28 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 28 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.-82+12463_-82+1246 others(11): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673216 | ||||||
| chr8:144673216
|
C | CAAAAAAA others(1): Show |
36 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(33): Show | 36 | HG01891.hp1 HG02109.hp1 HG02559.hp2 others(33): Show |
intron_variant | MODIFIER | c.-82+12462_-82+1246 others(12): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673216 | ||||||
| chr8:144673372
|
T | C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+12314A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673372 | ||||||
| chr8:144673374
|
T | G | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+12312A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673374 | ||||||
| chr8:144673412
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-82+12274T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673412 | ||||||
| chr8:144673481
|
A | C | 8 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+12205T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673481 | ||||||
| chr8:144673646
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+12040G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673646 | ||||||
| chr8:144673742
|
C | T | 1 | a0001c0007t0017g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-82+11944G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673742 | ||||||
| chr8:144673776
|
C | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+11910G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673776 | ||||||
| chr8:144673816
|
G | A | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+11870C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673816 | ||||||
| chr8:144673992
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-82+11694C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673992 | ||||||
| chr8:144673997
|
T | C | 3 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0018g0022 | 3 | HG02258.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-82+11689A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144673997 | ||||||
| chr8:144674123
|
G | C | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+11563C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674123 | ||||||
| chr8:144674135
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-82+11551C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674135 | ||||||
| chr8:144674289
|
C | T | 5 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0204others(2): Show | 5 | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82+11397G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674289 | ||||||
| chr8:144674340
|
G | A | 3 | a0001c0001t0008g0120a0001c0001t0008g0121a0001c0001t0008g0166 | 3 | HG02145.hp1 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-82+11346C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674340 | ||||||
| chr8:144674487
|
T | C | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+11199A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674487 | ||||||
| chr8:144674520
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-82+11166G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674520 | ||||||
| chr8:144674765
|
C | T | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+10921G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674765 | ||||||
| chr8:144674933
|
C | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0123 | 2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-82+10753G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144674933 | ||||||
| chr8:144675159
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+10527T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675159 | ||||||
| chr8:144675257
|
A | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+10429T>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675257 | ||||||
| chr8:144675396
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-82+10290G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675396 | ||||||
| chr8:144675506
|
G | A | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+10180C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675506 | ||||||
| chr8:144675551
|
C | T | 1 | a0001c0003t0001g0014 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-82+10135G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675551 | ||||||
| chr8:144675599
|
T | C | 71 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(68): Show | 71 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(68): Show |
intron_variant | MODIFIER | c.-82+10087A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675599 | ||||||
| chr8:144675708
|
T | C | 69 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(66): Show | 69 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(66): Show |
intron_variant | MODIFIER | c.-82+9978A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675708 | ||||||
| chr8:144675716
|
C | T | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+9970G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675716 | ||||||
| chr8:144675729
|
C | A | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+9957G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675729 | ||||||
| chr8:144675776
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+9910G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675776 | ||||||
| chr8:144675806
|
G | A | 2 | a0001c0001t0002g0145a0001c0003t0001g0012 | 2 | HG00280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-82+9880C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675806 | ||||||
| chr8:144675852
|
G | C | 6 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG01074.hp2 HG01167.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82+9834C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675852 | ||||||
| chr8:144675968
|
G | A | 1 | a0002c0008t0001g0067 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-82+9718C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144675968 | ||||||
| chr8:144676055
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-82+9631A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676055 | ||||||
| chr8:144676067
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-82+9619C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676067 | ||||||
| chr8:144676076
|
G | C | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+9610C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676076 | ||||||
| chr8:144676417
|
GGTGCTGC others(36): Show |
G | 69 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(66): Show | 69 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(66): Show |
intron_variant | MODIFIER | c.-82+9226_-82+9268d others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676417 | ||||||
| chr8:144676460
|
C | T | 4 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-82+9226G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676460 | ||||||
| chr8:144676664
|
C | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.-82+9022G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676664 | ||||||
| chr8:144676686
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-82+9000C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676686 | ||||||
| chr8:144676738
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-82+8948C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676738 | ||||||
| chr8:144676794
|
G | A | 1 | a0001c0002t0019g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-82+8892C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676794 | ||||||
| chr8:144676822
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+8864G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144676822 | ||||||
| chr8:144677057
|
C | T | 1 | a0001c0001t0007g0168 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-82+8629G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677057 | ||||||
| chr8:144677246
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+8440G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677246 | ||||||
| chr8:144677581
|
G | A | 10 | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(7): Show | 10 | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+8105C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677581 | ||||||
| chr8:144677599
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.-82+8087G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677599 | ||||||
| chr8:144677610
|
C | G | 1 | a0001c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-82+8076G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677610 | ||||||
| chr8:144677662
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-82+8024A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677662 | ||||||
| chr8:144677692
|
C | A | 190 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(187): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-82+7994G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677692 | ||||||
| chr8:144677706
|
T | C | 1 | a0001c0001t0004g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-82+7980A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677706 | ||||||
| chr8:144677996
|
A | C | 1 | a0001c0001t0020g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82+7690T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144677996 | ||||||
| chr8:144678078
|
C | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-82+7608G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678078 | ||||||
| chr8:144678116
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+7570G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678116 | ||||||
| chr8:144678191
|
G | A | 8 | a0001c0001t0002g0131a0001c0001t0007g0168a0001c0002t0001g0126others(5): Show | 8 | HG01192.hp2 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+7495C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678191 | ||||||
| chr8:144678426
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0135others(15): Show | 18 | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-82+7260C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678426 | ||||||
| chr8:144678587
|
G | A | 1 | a0001c0002t0001g0147 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-82+7099C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678587 | ||||||
| chr8:144678621
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02027.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-82+7065C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678621 | ||||||
| chr8:144678705
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-82+6981T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144678705 | ||||||
| chr8:144679038
|
A | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(187): Show | 190 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-82+6648T>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679038 | ||||||
| chr8:144679083
|
G | A | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-82+6603C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679083 | ||||||
| chr8:144679235
|
G | A | 3 | a0001c0004t0006g0073a0001c0004t0006g0074a0001c0004t0006g0075 | 3 | HG02886.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-82+6451C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679235 | ||||||
| chr8:144679276
|
T | G | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-82+6410A>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679276 | ||||||
| chr8:144679321
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82+6365C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679321 | ||||||
| chr8:144679511
|
G | A | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+6175C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679511 | ||||||
| chr8:144679702
|
C | T | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-82+5984G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679702 | ||||||
| chr8:144679709
|
A | G | 1 | a0001c0002t0001g0162 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-82+5977T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679709 | ||||||
| chr8:144679751
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-82+5935G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679751 | ||||||
| chr8:144679797
|
A | G | 1 | a0001c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-82+5889T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679797 | ||||||
| chr8:144679854
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+5832G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679854 | ||||||
| chr8:144679877
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0014g0054a0001c0002t0001g0051 | 3 | HG00438.hp1 NA18990.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-82+5809C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679877 | ||||||
| chr8:144679929
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-82+5757C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144679929 | ||||||
| chr8:144680082
|
G | A | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-82+5604C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144680082 | ||||||
| chr8:144680583
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+5103G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144680583 | ||||||
| chr8:144680623
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+5063T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144680623 | ||||||
| chr8:144680869
|
G | A | 16 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(13): Show | 16 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-82+4817C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144680869 | ||||||
| chr8:144680991
|
C | T | 2 | a0001c0002t0001g0020a0001c0007t0017g0019 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-82+4695G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144680991 | ||||||
| chr8:144681157
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-82+4529C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681157 | ||||||
| chr8:144681281
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-82+4405C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681281 | ||||||
| chr8:144681327
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-82+4359C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681327 | ||||||
| chr8:144681421
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+4265T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681421 | ||||||
| chr8:144681464
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+4222G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681464 | ||||||
| chr8:144681565
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-82+4121G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681565 | ||||||
| chr8:144681568
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-82+4118G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681568 | ||||||
| chr8:144681697
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-82+3989T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681697 | ||||||
| chr8:144681702
|
A | G | 69 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(66): Show | 69 | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(66): Show |
intron_variant | MODIFIER | c.-82+3984T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681702 | ||||||
| chr8:144681876
|
TA | T | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-82+3809delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681876 | ||||||
| chr8:144681962
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-82+3724A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144681962 | ||||||
| chr8:144682051
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-82+3635C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682051 | ||||||
| chr8:144682064
|
C | A | 10 | a0001c0001t0001g0151a0001c0001t0002g0157a0001c0001t0004g0150others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82+3622G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682064 | ||||||
| chr8:144682065
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-82+3621C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682065 | ||||||
| chr8:144682242
|
C | T | 13 | a0001c0001t0003g0023a0001c0001t0003g0063a0001c0001t0003g0068others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+3444G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682242 | ||||||
| chr8:144682244
|
C | CA | 45 | a0001c0001t0001g0053a0001c0001t0001g0163a0001c0001t0001g0208others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-82+3441dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682244 | ||||||
| chr8:144682244
|
CA | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 14 | HG01516.hp2 HG02004.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.-82+3441delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682244 | ||||||
| chr8:144682406
|
A | G | 1 | a0001c0007t0003g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-82+3280T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682406 | ||||||
| chr8:144682442
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-82+3244C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682442 | ||||||
| chr8:144682481
|
G | A | 55 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(52): Show | 55 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-82+3205C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682481 | ||||||
| chr8:144682541
|
T | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+3145A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682541 | ||||||
| chr8:144682548
|
C | CA | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0002t0001g0214others(5): Show | 8 | HG00438.hp2 HG02145.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-82+3137dupT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682548 | ||||||
| chr8:144682548
|
CA | C | 23 | a0001c0001t0001g0026a0001c0001t0001g0065a0001c0001t0001g0077others(20): Show | 23 | HG01070.hp2 HG01074.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-82+3137delT | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682548 | ||||||
| chr8:144682548
|
CAA | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0055others(16): Show | 19 | HG02258.hp1 HG02280.hp1 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.-82+3136_-82+3137d others(4): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682548 | ||||||
| chr8:144682548
|
CAAA | C | 33 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 33 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.-82+3135_-82+3137d others(5): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682548 | ||||||
| chr8:144682714
|
A | G | 1 | a0001c0002t0009g0028 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-82+2972T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682714 | ||||||
| chr8:144682792
|
C | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+2894G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682792 | ||||||
| chr8:144682939
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-82+2747G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682939 | ||||||
| chr8:144682981
|
C | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-82+2705G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144682981 | ||||||
| chr8:144683143
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-82+2543C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683143 | ||||||
| chr8:144683247
|
A | G | 1 | a0001c0002t0001g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-82+2439T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683247 | ||||||
| chr8:144683387
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG00558.hp1 NA18997.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+2299T>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683387 | ||||||
| chr8:144683405
|
T | C | 17 | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(14): Show | 17 | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-82+2281A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683405 | ||||||
| chr8:144683457
|
C | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(26): Show | 29 | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82+2229G>C | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683457 | ||||||
| chr8:144683491
|
CGTGAGCC others(128): Show |
C | 1 | a0001c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-82+2060_-82+2194d others(2): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683491 | ||||||
| chr8:144683500
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-82+2186G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683500 | ||||||
| chr8:144683594
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-82+2092C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683594 | ||||||
| chr8:144683613
|
C | T | 2 | a0001c0001t0007g0018a0001c0007t0001g0017 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-82+2073G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144683613 | ||||||
| chr8:144684012
|
T | A | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-82+1674A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684012 | ||||||
| chr8:144684021
|
T | A | 1 | a0001c0002t0023g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-82+1665A>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684021 | ||||||
| chr8:144684121
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-82+1565G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684121 | ||||||
| chr8:144684342
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+1344C>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684342 | ||||||
| chr8:144684353
|
C | T | 2 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-82+1333G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684353 | ||||||
| chr8:144684605
|
ACAGCTGC others(19): Show |
A | 1 | a0001c0002t0001g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-82+1055_-82+1080d others(28): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684605 | ||||||
| chr8:144684649
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-82+1037G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684649 | ||||||
| chr8:144684904
|
G | A | 1 | a0001c0001t0005g0243 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-82+782C>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144684904 | ||||||
| chr8:144685114
|
GGGGCACA others(19): Show |
G | 5 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0002t0001g0020others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82+546_-82+571del others(26): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685114 | ||||||
| chr8:144685129
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82+557G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685129 | ||||||
| chr8:144685239
|
GTGGACAG others(20): Show |
G | 13 | a0001c0002t0001g0003a0001c0002t0001g0007a0001c0002t0001g0013others(10): Show | 13 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-82+420_-82+446del others(27): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685239 | ||||||
| chr8:144685260
|
C | T | 1 | a0001c0002t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-82+426G>A | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685260 | ||||||
| chr8:144685426
|
C | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | NA18963.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-82+260G>T | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685426 | ||||||
| chr8:144685646
|
T | C | 245 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-82+40A>G | ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | 144685646 |