| geneid | 26084 |
|---|---|
| ensemblid | ENSG00000114790.13 |
| hgncid | 24490 |
| symbol | ARHGEF26 |
| name | Rho guanine nucleotide exchange factor 26 |
| refseq_nuc | NM_015595.4 |
| refseq_prot | NP_056410.3 |
| ensembl_nuc | ENST00000465093.6 |
| ensembl_prot | ENSP00000423418.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 154121390 |
| end | 154257825 |
| strand | + |
| ver | v1.2 |
| region | chr3:154121390-154257825 |
| region5000 | chr3:154116390-154262825 |
| regionname0 | ARHGEF26_chr3_154121390_154257825 |
| regionname5000 | ARHGEF26_chr3_154116390_154262825 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 871 | 154 | 32 | 33 | 61 | 11 | 16 | 45 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002 | 0/0 | 871 | 105 | 23 | 12 | 58 | 3 | 9 | 41 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003 | 0/0 | 871 | 10 | 2 | 7 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0004 | 0/0 | 871 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0005 | 0/0 | 871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0006 | 0/0 | 871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0007 | 0/0 | 871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0008 | 0/0 | 871 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0009 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0010 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0011 | 0/0 | 871 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0012 | 0/0 | 871 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2616 | 151 | 32 | 31 | 61 | 11 | 15 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0002 | 0/0 | 2616 | 64 | 5 | 9 | 40 | 3 | 7 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0003 | 0/0 | 2616 | 38 | 16 | 3 | 18 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0004 | 0/0 | 2616 | 10 | 2 | 7 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0005 | 0/0 | 2616 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0006 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0007 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0008 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0009 | 0/0 | 2616 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0010 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0011 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0012 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0013 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0014 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0015 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0016 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0017 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| c0018 | 0/0 | 2616 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2535 | 41 | 7 | 8 | 21 | 2 | 3 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0002 | 0/1 | 2534 | 37 | 0 | 9 | 17 | 5 | 5 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0003 | 0/0 | 2536 | 37 | 1 | 7 | 24 | 1 | 4 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0004 | 0/0 | 2536 | 29 | 6 | 6 | 13 | 4 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0005 | 0/0 | 2535 | 22 | 6 | 2 | 13 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0006 | 0/0 | 2536 | 14 | 1 | 1 | 12 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0007 | 0/0 | 2536 | 10 | 1 | 3 | 4 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0008 | 0/0 | 2537 | 8 | 1 | 0 | 5 | 1 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0009 | 0/0 | 2533 | 7 | 3 | 2 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0010 | 0/0 | 2534 | 6 | 1 | 3 | 0 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0011 | 0/0 | 2535 | 4 | 0 | 2 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0012 | 0/0 | 2537 | 4 | 0 | 1 | 2 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0013 | 0/0 | 2535 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0014 | 0/0 | 2533 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0015 | 0/0 | 2532 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0016 | 0/0 | 2534 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0017 | 0/0 | 2536 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0018 | 0/0 | 2537 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0019 | 0/0 | 2534 | 3 | 1 | 0 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0020 | 0/0 | 2536 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0021 | 0/0 | 2535 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0022 | 0/0 | 2535 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0023 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0024 | 0/0 | 2535 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0025 | 0/0 | 2533 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0026 | 0/0 | 2534 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0027 | 0/0 | 2535 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0028 | 0/0 | 2536 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0029 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0030 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0031 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0032 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0033 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0034 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0035 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0036 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0037 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0038 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0039 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0040 | 0/0 | 2533 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0041 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0042 | 0/0 | 2534 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0043 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0044 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0045 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0046 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0047 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0048 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0049 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0050 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0051 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| t0052 | 0/0 | 2536 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2616 | 151 | 32 | 31 | 61 | 11 | 15 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0009 | 0/0 | 2616 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0015 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002 | 0/0 | 2616 | 64 | 5 | 9 | 40 | 3 | 7 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003 | 0/0 | 2616 | 38 | 16 | 3 | 18 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0007 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0014 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004 | 0/0 | 2616 | 10 | 2 | 7 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0004c0005 | 0/0 | 2616 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0005c0008 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0006c0012 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0006c0013 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0007c0006 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0008c0017 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0009c0016 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0010c0011 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0011c0018 | 0/0 | 2616 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0012c0010 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5150 | 40 | 7 | 8 | 20 | 2 | 3 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0002 | 0/1 | 5149 | 33 | 0 | 8 | 17 | 4 | 3 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0004 | 0/0 | 5151 | 26 | 4 | 5 | 13 | 4 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0007 | 0/0 | 5151 | 9 | 1 | 2 | 4 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0009 | 0/0 | 5148 | 7 | 3 | 2 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0010 | 0/0 | 5149 | 3 | 1 | 0 | 0 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0011 | 0/0 | 5150 | 4 | 0 | 2 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0012 | 0/0 | 5152 | 4 | 0 | 1 | 2 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0013 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0014 | 0/0 | 5148 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0015 | 0/0 | 5147 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0016 | 0/0 | 5149 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0017 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0020 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0021 | 0/0 | 5150 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0023 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0029 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0030 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0033 | 0/0 | 5150 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0034 | 0/0 | 5150 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0035 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0036 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0037 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0039 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0041 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0001t0043 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0009t0022 | 0/0 | 5150 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0001c0015t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0003 | 0/0 | 5151 | 34 | 0 | 6 | 23 | 1 | 4 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0005 | 0/0 | 5150 | 6 | 3 | 1 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0006 | 0/0 | 5151 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0008 | 0/0 | 5152 | 7 | 0 | 0 | 5 | 1 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0019 | 0/0 | 5149 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0024 | 0/0 | 5150 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0027 | 0/0 | 5150 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0028 | 0/0 | 5151 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0047 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0049 | 0/0 | 5150 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0051 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0002t0052 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0003 | 0/0 | 5151 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0004 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0005 | 0/0 | 5150 | 15 | 2 | 1 | 11 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0006 | 0/0 | 5151 | 7 | 1 | 1 | 5 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0018 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0019 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0025 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0026 | 0/0 | 5149 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0027 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0044 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0045 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0046 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0048 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0003t0050 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0007t0018 | 0/0 | 5152 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0002c0014t0019 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0002 | 0/0 | 5149 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0004 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0010 | 0/0 | 5149 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0031 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0032 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0038 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0040 | 0/0 | 5148 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0003c0004t0042 | 0/0 | 5149 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0004c0005t0013 | 0/0 | 5150 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0005c0008t0014 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0005c0008t0023 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0006c0012t0008 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0006c0013t0025 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0007c0006t0017 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0008c0017t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0009c0016t0001 | 0/0 | 5150 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0010c0011t0005 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0011c0018t0007 | 0/0 | 5151 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| a0012c0010t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | copy fasta | chr3 | 154116390 | 154262825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0013g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0014g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0016g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0016g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0016g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0017g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0020g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0021g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0021g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0023g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0029g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0030g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0033g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0034g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0035g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0036g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0037g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0039g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0041g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0043g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0009t0022g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0009t0022g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0015t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0019g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0024g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0024g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0027g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0028g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0028g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0047g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0049g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0051g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0052g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0018g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0019g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0025g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0026g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0026g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0027g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0044g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0045g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0046g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0048g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0050g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0007t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0007t0018g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0014t0019g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0010g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0010g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0031g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0032g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0038g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0040g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0042g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0013g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0005c0008t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0005c0008t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0006c0012t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0006c0013t0025g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0007c0006t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0007c0006t0017g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0008c0017t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0009c0016t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0010c0011t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0011c0018t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0012c0010t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0137 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0171 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00140 | hp1 | a0001 | c0001 | t0020 | g0003 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0265 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00323 | hp1 | a0003 | c0004 | t0040 | g0014 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0250 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00408 | hp1 | a0002 | c0003 | t0005 | g0113 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00438 | hp1 | a0002 | c0003 | t0005 | g0108 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00544 | hp1 | a0002 | c0003 | t0005 | g0114 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00544 | hp2 | a0001 | c0001 | t0034 | g0202 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00558 | hp1 | a0009 | c0016 | t0001 | g0218 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00597 | hp1 | a0002 | c0002 | t0006 | g0059 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00609 | hp1 | a0002 | c0003 | t0005 | g0116 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00621 | hp1 | a0002 | c0003 | t0026 | g0110 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0228 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0196 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00741 | hp2 | a0003 | c0004 | t0010 | g0013 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01069 | hp1 | a0002 | c0003 | t0003 | g0089 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01071 | hp2 | a0001 | c0001 | t0020 | g0003 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01081 | hp1 | a0002 | c0002 | t0052 | g0082 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01081 | hp2 | a0003 | c0004 | t0004 | g0011 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0038 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01099 | hp2 | a0003 | c0004 | t0038 | g0012 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01106 | hp1 | a0003 | c0004 | t0010 | g0009 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0227 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01167 | hp2 | a0001 | c0009 | t0022 | g0164 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01169 | hp1 | a0001 | c0009 | t0022 | g0163 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0243 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01243 | hp1 | a0004 | c0005 | t0013 | g0158 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01243 | hp2 | a0002 | c0002 | t0005 | g0042 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0206 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01255 | hp2 | a0003 | c0004 | t0042 | g0016 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0067 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01258 | hp2 | a0003 | c0004 | t0010 | g0015 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0220 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0246 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01358 | hp1 | a0003 | c0004 | t0002 | g0007 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01361 | hp2 | a0002 | c0003 | t0005 | g0118 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01433 | hp1 | a0002 | c0003 | t0006 | g0096 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01496 | hp1 | a0011 | c0018 | t0007 | g0006 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0219 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01516 | hp1 | a0008 | c0017 | t0002 | g0170 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01516 | hp2 | a0002 | c0002 | t0003 | g0037 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01517 | hp2 | a0002 | c0002 | t0008 | g0036 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01884 | hp1 | a0002 | c0003 | t0026 | g0103 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01884 | hp2 | a0007 | c0006 | t0017 | g0129 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0131 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0079 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01975 | hp1 | a0001 | c0001 | t0016 | g0186 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0031 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0066 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0053 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02055 | hp1 | a0006 | c0012 | t0008 | g0018 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02055 | hp2 | a0005 | c0008 | t0023 | g0123 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02056 | hp1 | a0002 | c0003 | t0005 | g0120 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02071 | hp2 | a0002 | c0002 | t0024 | g0062 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02074 | hp1 | a0002 | c0002 | t0003 | g0065 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02132 | hp2 | a0002 | c0003 | t0005 | g0109 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02135 | hp2 | a0002 | c0003 | t0006 | g0111 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02145 | hp1 | a0001 | c0001 | t0037 | g0256 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0127 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02155 | hp2 | a0002 | c0003 | t0005 | g0107 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0057 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02257 | hp2 | a0010 | c0011 | t0005 | g0017 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02258 | hp2 | a0002 | c0003 | t0019 | g0102 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0124 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02523 | hp1 | a0002 | c0002 | t0005 | g0021 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02572 | hp1 | a0001 | c0001 | t0030 | g0125 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0144 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02602 | hp2 | a0012 | c0010 | t0002 | g0241 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02622 | hp2 | a0002 | c0003 | t0004 | g0086 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02630 | hp1 | a0004 | c0005 | t0013 | g0136 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02630 | hp2 | a0002 | c0003 | t0050 | g0099 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0126 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0133 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02735 | hp1 | a0002 | c0002 | t0049 | g0055 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0132 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02818 | hp1 | a0007 | c0006 | t0017 | g0128 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0276 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02886 | hp2 | a0001 | c0001 | t0035 | g0255 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02922 | hp2 | a0006 | c0013 | t0025 | g0019 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0154 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03041 | hp2 | a0002 | c0002 | t0051 | g0033 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03098 | hp1 | a0005 | c0008 | t0014 | g0122 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03098 | hp2 | a0002 | c0002 | t0005 | g0043 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03195 | hp1 | a0002 | c0007 | t0018 | g0090 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03195 | hp2 | a0003 | c0004 | t0032 | g0008 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03209 | hp1 | a0002 | c0003 | t0003 | g0098 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03209 | hp2 | a0002 | c0003 | t0027 | g0104 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03225 | hp1 | a0002 | c0003 | t0004 | g0085 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03225 | hp2 | a0002 | c0002 | t0005 | g0034 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0140 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03239 | hp2 | a0001 | c0001 | t0029 | g0151 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03453 | hp1 | a0002 | c0003 | t0044 | g0094 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0135 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0050 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0160 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03516 | hp1 | a0002 | c0007 | t0018 | g0091 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03579 | hp1 | a0002 | c0003 | t0048 | g0097 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03579 | hp2 | a0001 | c0001 | t0043 | g0134 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03669 | hp1 | a0001 | c0001 | t0033 | g0221 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0141 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03710 | hp2 | a0001 | c0001 | t0021 | g0212 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0178 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03834 | hp2 | a0002 | c0014 | t0019 | g0040 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03927 | hp1 | a0002 | c0003 | t0005 | g0112 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0239 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG04115 | hp1 | a0002 | c0002 | t0008 | g0020 | SAS | STU | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG04115 | hp2 | a0001 | c0015 | t0002 | g0143 | SAS | STU | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18522 | hp1 | a0002 | c0003 | t0025 | g0105 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0047 | EAS | CHB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18906 | hp1 | a0002 | c0003 | t0006 | g0088 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18946 | hp2 | a0002 | c0002 | t0006 | g0029 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18947 | hp1 | a0002 | c0003 | t0003 | g0106 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18948 | hp1 | a0002 | c0003 | t0006 | g0100 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18951 | hp2 | a0001 | c0001 | t0016 | g0264 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18954 | hp1 | a0002 | c0002 | t0006 | g0048 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0244 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0267 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18962 | hp1 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18962 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0061 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18967 | hp2 | a0002 | c0002 | t0006 | g0027 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18969 | hp2 | a0002 | c0003 | t0005 | g0119 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18970 | hp1 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18970 | hp2 | a0002 | c0002 | t0008 | g0072 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18978 | hp1 | a0002 | c0003 | t0006 | g0101 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18979 | hp1 | a0002 | c0002 | t0019 | g0056 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18983 | hp2 | a0002 | c0002 | t0006 | g0063 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18984 | hp2 | a0002 | c0002 | t0027 | g0046 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18985 | hp1 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18986 | hp2 | a0002 | c0002 | t0008 | g0032 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18989 | hp2 | a0002 | c0002 | t0005 | g0060 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18994 | hp2 | a0002 | c0002 | t0006 | g0030 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18999 | hp2 | a0002 | c0002 | t0008 | g0074 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19001 | hp1 | a0002 | c0002 | t0008 | g0081 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19006 | hp2 | a0001 | c0001 | t0012 | g0166 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19007 | hp2 | a0002 | c0002 | t0006 | g0058 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0277 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19030 | hp2 | a0002 | c0003 | t0045 | g0095 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19043 | hp1 | a0003 | c0004 | t0031 | g0010 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19043 | hp2 | a0002 | c0003 | t0046 | g0093 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19054 | hp2 | a0002 | c0003 | t0006 | g0117 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19060 | hp2 | a0001 | c0001 | t0012 | g0263 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19070 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19082 | hp2 | a0002 | c0002 | t0008 | g0080 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19084 | hp1 | a0002 | c0003 | t0006 | g0115 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19086 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19090 | hp1 | a0002 | c0003 | t0005 | g0121 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0270 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19240 | hp1 | a0001 | c0001 | t0039 | g0275 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0261 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20129 | hp1 | a0002 | c0002 | t0047 | g0041 | AFR | ASW | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20129 | hp2 | a0004 | c0005 | t0013 | g0159 | AFR | ASW | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20805 | hp1 | a0002 | c0002 | t0028 | g0078 | EUR | TSI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20905 | hp1 | a0002 | c0002 | t0024 | g0035 | SAS | GIH | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | GIH | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01123 | hp2 | a0002 | c0002 | t0028 | g0077 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02109 | hp1 | a0001 | c0001 | t0036 | g0205 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02109 | hp2 | a0002 | c0003 | t0005 | g0087 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG06807 | hp1 | a0001 | c0001 | t0041 | g0165 | AFR | USA | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0138 | AFR | USA | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA21309 | hp1 | a0002 | c0003 | t0018 | g0092 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA21309 | hp2 | a0002 | c0002 | t0005 | g0028 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0232 | REF | REF | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:154122017
|
T | A | 1 | a0012 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.25T>A | p.Phe9Ile | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 206/5149 | 25/2616 | 9/871 | chr3 | 154122017 | ||
| chr3:154122077
|
G | C | 10 | a0001a0002a0004others(7): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
missense_variant | MODERATE | c.85G>C | p.Val29Leu | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 266/5149 | 85/2616 | 29/871 | chr3 | 154122077 | ||
| chr3:154122078
|
T | G | 1 | a0007 | 2 | HG01884.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.86T>G | p.Val29Gly | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 267/5149 | 86/2616 | 29/871 | chr3 | 154122078 | ||
| chr3:154122158
|
G | C | 1 | a0010 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.166G>C | p.Gly56Arg | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 347/5149 | 166/2616 | 56/871 | chr3 | 154122158 | ||
| chr3:154122170
|
C | T | 5 | a0001a0004a0008others(2): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
missense_variant | MODERATE | c.178C>T | p.Leu60Phe | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 359/5149 | 178/2616 | 60/871 | chr3 | 154122170 | ||
| chr3:154122171
|
T | C | 10 | a0001a0002a0004others(7): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
missense_variant | MODERATE | c.179T>C | p.Leu60Pro | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 360/5149 | 179/2616 | 60/871 | chr3 | 154122171 | ||
| chr3:154122306
|
C | T | 1 | a0008 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.314C>T | p.Ser105Phe | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 495/5149 | 314/2616 | 105/871 | chr3 | 154122306 | ||
| chr3:154122539
|
G | C | 2 | a0006a0010 | 3 | HG02055.hp1 HG02257.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.547G>C | p.Asp183His | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 728/5149 | 547/2616 | 183/871 | chr3 | 154122539 | ||
| chr3:154122600
|
T | C | 4 | a0002a0006a0010others(1): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
missense_variant | MODERATE | c.608T>C | p.Phe203Ser | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 789/5149 | 608/2616 | 203/871 | chr3 | 154122600 | ||
| chr3:154191415
|
G | A | 1 | a0004 | 3 | HG01243.hp1 HG02630.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.1767G>A | p.Met589Ile | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/15 | 1948/5149 | 1767/2616 | 589/871 | chr3 | 154191415 | ||
| chr3:154254813
|
G | A | 1 | a0009 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.2462G>A | p.Arg821His | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/15 | 2643/5149 | 2462/2616 | 821/871 | chr3 | 154254813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:154122373
|
C | T | 6 | a0002c0002a0002c0014a0006c0012others(3): Show | 69 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(66): Show |
synonymous_variant | LOW | c.381C>T | p.Ser127Ser | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 562/5149 | 381/2616 | 127/871 | chr3 | 154122373 | ||
| chr3:154122478
|
T | C | 1 | a0002c0007 | 2 | HG03195.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.486T>C | p.Leu162Leu | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 667/5149 | 486/2616 | 162/871 | chr3 | 154122478 | ||
| chr3:154217898
|
G | A | 1 | a0001c0009 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.1875G>A | p.Arg625Arg | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/15 | 2056/5149 | 1875/2616 | 625/871 | chr3 | 154217898 | ||
| chr3:154217943
|
G | A | 1 | a0006c0012 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1920G>A | p.Leu640Leu | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/15 | 2101/5149 | 1920/2616 | 640/871 | chr3 | 154217943 | ||
| chr3:154240454
|
T | C | 1 | a0001c0015 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.2175T>C | p.Ser725Ser | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/15 | 2356/5149 | 2175/2616 | 725/871 | chr3 | 154240454 | ||
| chr3:154240538
|
C | T | 1 | a0002c0014 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.2259C>T | p.His753His | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/15 | 2440/5149 | 2259/2616 | 753/871 | chr3 | 154240538 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:154121418
|
C | G | 30 | a0002c0002t0003a0002c0002t0005a0002c0002t0006others(27): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-153C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/15 | 575 | chr3 | 154121418 | |||||
| chr3:154121422
|
G | C | 5 | a0002c0003t0018a0002c0003t0044a0002c0003t0045others(2): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-149G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/15 | 571 | chr3 | 154121422 | |||||
| chr3:154121456
|
C | T | 1 | a0002c0002t0028 | 2 | HG01123.hp2 NA20805.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/15 | chr3 | 154121456 | ||||||
| chr3:154121948
|
C | T | 1 | a0002c0002t0052 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-45C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/15 | 45 | chr3 | 154121948 | |||||
| chr3:154255501
|
A | G | 1 | a0002c0002t0051 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 28 | chr3 | 154255501 | |||||
| chr3:154255619
|
T | C | 15 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(12): Show | 58 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*146T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 146 | chr3 | 154255619 | |||||
| chr3:154255795
|
T | TA | 2 | a0001c0001t0014a0005c0008t0014 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*323dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 324 | INFO_REALIGN_3_PRIME | chr3 | 154255795 | ||||
| chr3:154256098
|
T | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(36): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*625T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 625 | chr3 | 154256098 | |||||
| chr3:154256109
|
A | T | 6 | a0001c0001t0013a0001c0001t0023a0001c0001t0035others(3): Show | 8 | HG01243.hp1 HG01346.hp2 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 636 | chr3 | 154256109 | |||||
| chr3:154256137
|
T | G | 74 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(71): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*664T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 664 | chr3 | 154256137 | |||||
| chr3:154256169
|
C | T | 2 | a0001c0001t0041a0001c0009t0022 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*696C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 696 | chr3 | 154256169 | |||||
| chr3:154256231
|
C | G | 1 | a0001c0001t0035 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 758 | chr3 | 154256231 | |||||
| chr3:154256240
|
T | C | 25 | a0001c0001t0007a0001c0001t0017a0001c0001t0021others(22): Show | 78 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*767T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 767 | chr3 | 154256240 | |||||
| chr3:154256447
|
C | T | 3 | a0001c0001t0017a0002c0003t0050a0007c0006t0017 | 4 | HG01884.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 974 | chr3 | 154256447 | |||||
| chr3:154256468
|
C | G | 1 | a0001c0001t0029 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*995C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 995 | chr3 | 154256468 | |||||
| chr3:154256548
|
T | TA | 24 | a0001c0001t0004a0001c0001t0007a0001c0001t0015others(21): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1102dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1103 | INFO_REALIGN_3_PRIME | chr3 | 154256548 | ||||
| chr3:154256548
|
T | TAA | 6 | a0001c0001t0012a0001c0001t0030a0001c0001t0036others(3): Show | 15 | HG00741.hp1 HG01517.hp2 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1101_*1102dupAA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1103 | INFO_REALIGN_3_PRIME | chr3 | 154256548 | ||||
| chr3:154256549
|
A | T | 1 | a0001c0001t0034 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1076A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1076 | chr3 | 154256549 | |||||
| chr3:154256565
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0051 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1093_*1103delAAAA others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1093 | chr3 | 154256565 | |||||
| chr3:154256567
|
A | C | 1 | a0001c0001t0033 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1094A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1094 | chr3 | 154256567 | |||||
| chr3:154256574
|
AAC | A | 3 | a0001c0001t0009a0002c0003t0025a0006c0013t0025 | 9 | HG00738.hp2 HG01167.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1102_*1103delAC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1102 | chr3 | 154256574 | |||||
| chr3:154256575
|
AC | A | 13 | a0001c0001t0002a0001c0001t0016a0001c0001t0029others(10): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1104delC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1104 | INFO_REALIGN_3_PRIME | chr3 | 154256575 | ||||
| chr3:154256576
|
C | A | 54 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(51): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1103C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1103 | chr3 | 154256576 | |||||
| chr3:154256601
|
C | A | 25 | a0001c0001t0007a0001c0001t0017a0001c0001t0021others(22): Show | 78 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1128C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1128 | chr3 | 154256601 | |||||
| chr3:154256626
|
A | G | 1 | a0001c0001t0030 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1153 | chr3 | 154256626 | |||||
| chr3:154256728
|
C | T | 1 | a0001c0001t0035 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1255C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1255 | chr3 | 154256728 | |||||
| chr3:154256817
|
C | CAG | 3 | a0001c0001t0023a0001c0001t0043a0005c0008t0023 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1347_*1348dupAG | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1349 | INFO_REALIGN_3_PRIME | chr3 | 154256817 | ||||
| chr3:154256886
|
T | TTATC | 2 | a0003c0004t0031a0003c0004t0032 | 2 | HG03195.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1415_*1418dupATCT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1419 | INFO_REALIGN_3_PRIME | chr3 | 154256886 | ||||
| chr3:154256938
|
G | A | 1 | a0002c0002t0047 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1465 | chr3 | 154256938 | |||||
| chr3:154257054
|
AACT | A | 2 | a0001c0001t0014a0005c0008t0014 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1585_*1587delACT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 1585 | INFO_REALIGN_3_PRIME | chr3 | 154257054 | ||||
| chr3:154257634
|
GTGTT | G | 3 | a0001c0001t0015a0001c0001t0030a0002c0003t0044 | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2168_*2171delTTTG | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 2168 | INFO_REALIGN_3_PRIME | chr3 | 154257634 | ||||
| chr3:154257666
|
A | AC | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*2193_*2194insC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 2194 | chr3 | 154257666 | |||||
| chr3:154257748
|
A | AT | 9 | a0001c0001t0017a0001c0001t0037a0002c0003t0018others(6): Show | 11 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2280dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 2281 | INFO_REALIGN_3_PRIME | chr3 | 154257748 | ||||
| chr3:154257776
|
T | C | 2 | a0001c0001t0041a0001c0009t0022 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2303T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 15/15 | 2303 | chr3 | 154257776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:154121585
|
A | C | 148 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(145): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-52+66A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/14 | chr3 | 154121585 | ||||||
| chr3:154121600
|
A | T | 1 | a0002c0003t0005g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-52+81A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/14 | chr3 | 154121600 | ||||||
| chr3:154121676
|
G | T | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-52+157G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/14 | chr3 | 154121676 | ||||||
| chr3:154121726
|
G | A | 1 | a0004c0005t0013g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-52+207G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/14 | chr3 | 154121726 | ||||||
| chr3:154121835
|
T | C | 107 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(104): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-51-107T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 1/14 | chr3 | 154121835 | ||||||
| chr3:154123109
|
C | G | 28 | a0002c0003t0003g0098a0002c0003t0003g0106a0002c0003t0005g0001others(25): Show | 29 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1083+34C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123109 | ||||||
| chr3:154123358
|
C | T | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1083+283C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123358 | ||||||
| chr3:154123365
|
A | G | 4 | a0001c0001t0007g0274a0001c0001t0014g0276a0001c0001t0014g0277others(1): Show | 4 | HG02258.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+290A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123365 | ||||||
| chr3:154123453
|
T | C | 4 | a0002c0003t0003g0098a0002c0003t0006g0096a0002c0003t0048g0097others(1): Show | 4 | HG01433.hp1 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+378T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123453 | ||||||
| chr3:154123511
|
T | A | 102 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(99): Show | 103 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1083+436T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123511 | ||||||
| chr3:154123574
|
T | C | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1083+499T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123574 | ||||||
| chr3:154123824
|
T | C | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1084-586T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154123824 | ||||||
| chr3:154123919
|
C | CAG | 276 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(273): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1084-489_1084-488d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 154123919 | |||||
| chr3:154124068
|
G | GT | 33 | a0002c0003t0003g0089a0002c0003t0003g0098a0002c0003t0003g0106others(30): Show | 34 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1084-336dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 154124068 | |||||
| chr3:154124139
|
G | A | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1084-271G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154124139 | ||||||
| chr3:154124161
|
G | A | 3 | a0006c0012t0008g0018a0006c0013t0025g0019a0010c0011t0005g0017 | 3 | HG02055.hp1 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1084-249G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154124161 | ||||||
| chr3:154124194
|
T | C | 3 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0010g0138 | 3 | HG00099.hp1 HG01109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1084-216T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | chr3 | 154124194 | ||||||
| chr3:154124372
|
C | CT | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0002g0271others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1084-20dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 154124372 | |||||
| chr3:154124372
|
C | CTTT | 9 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(6): Show | 9 | HG01496.hp1 HG02015.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-22_1084-20dup others(3): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 154124372 | |||||
| chr3:154124372
|
C | CTTTT | 92 | a0002c0002t0003g0031a0002c0002t0003g0037a0002c0002t0003g0038others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1084-23_1084-20dup others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr3 | 154124372 | |||||
| chr3:154124620
|
C | A | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1123+171C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154124620 | ||||||
| chr3:154124643
|
C | G | 5 | a0001c0001t0001g0130a0001c0001t0017g0132a0001c0001t0021g0133others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123+194C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154124643 | ||||||
| chr3:154124703
|
C | T | 1 | a0002c0002t0003g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1123+254C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154124703 | ||||||
| chr3:154124902
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1123+453A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154124902 | ||||||
| chr3:154124978
|
CA | C | 249 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0153others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1123+542delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 154124978 | |||||
| chr3:154125113
|
C | T | 1 | a0005c0008t0023g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1123+664C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125113 | ||||||
| chr3:154125163
|
A | G | 1 | a0001c0001t0004g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1123+714A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125163 | ||||||
| chr3:154125250
|
A | G | 1 | a0002c0002t0003g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1123+801A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125250 | ||||||
| chr3:154125341
|
A | G | 2 | a0002c0003t0003g0098a0002c0003t0050g0099 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1123+892A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125341 | ||||||
| chr3:154125362
|
G | T | 1 | a0001c0001t0043g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1123+913G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125362 | ||||||
| chr3:154125387
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1123+938T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125387 | ||||||
| chr3:154125471
|
C | G | 3 | a0001c0001t0001g0146a0001c0001t0004g0147a0001c0001t0004g0148 | 3 | HG00408.hp2 NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1123+1022C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125471 | ||||||
| chr3:154125686
|
T | C | 1 | a0001c0001t0004g0149 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1123+1237T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125686 | ||||||
| chr3:154125801
|
A | G | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1123+1352A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125801 | ||||||
| chr3:154125878
|
T | G | 151 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1123+1429T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154125878 | ||||||
| chr3:154126025
|
T | C | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1123+1576T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126025 | ||||||
| chr3:154126125
|
A | G | 1 | a0002c0002t0003g0083 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1123+1676A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126125 | ||||||
| chr3:154126167
|
G | C | 1 | a0001c0001t0004g0149 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1123+1718G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126167 | ||||||
| chr3:154126191
|
C | T | 1 | a0002c0002t0052g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1123+1742C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126191 | ||||||
| chr3:154126369
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1123+1920T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126369 | ||||||
| chr3:154126401
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1123+1952C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126401 | ||||||
| chr3:154126412
|
T | G | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1123+1963T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126412 | ||||||
| chr3:154126573
|
C | T | 107 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(104): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1123+2124C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126573 | ||||||
| chr3:154126792
|
T | A | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1123+2343T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154126792 | ||||||
| chr3:154127061
|
A | C | 1 | a0001c0001t0016g0264 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1124-2513A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154127061 | ||||||
| chr3:154127475
|
C | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0262a0001c0001t0012g0263 | 4 | NA19004.hp2 NA19060.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1124-2099C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154127475 | ||||||
| chr3:154127529
|
G | GTCA | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1124-2041_1124-203 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 154127529 | |||||
| chr3:154127600
|
ATT | A | 157 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1124-1957_1124-195 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 154127600 | |||||
| chr3:154127600
|
ATTT | A | 108 | a0001c0001t0009g0267a0002c0002t0003g0022a0002c0002t0003g0023others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1124-1958_1124-195 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr3 | 154127600 | |||||
| chr3:154127794
|
CAT | C | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1124-1779_1124-177 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154127794 | ||||||
| chr3:154127923
|
G | A | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1124-1651G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154127923 | ||||||
| chr3:154127953
|
C | T | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1124-1621C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154127953 | ||||||
| chr3:154128398
|
C | T | 1 | a0002c0002t0005g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1124-1176C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128398 | ||||||
| chr3:154128411
|
G | A | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1124-1163G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128411 | ||||||
| chr3:154128535
|
G | A | 155 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1124-1039G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128535 | ||||||
| chr3:154128692
|
A | G | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1124-882A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128692 | ||||||
| chr3:154128840
|
C | T | 2 | a0001c0001t0009g0004a0001c0001t0009g0261 | 3 | HG02280.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1124-734C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128840 | ||||||
| chr3:154128911
|
T | C | 146 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1124-663T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154128911 | ||||||
| chr3:154129257
|
A | T | 1 | a0001c0001t0002g0260 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1124-317A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154129257 | ||||||
| chr3:154129757
|
A | G | 1 | a0001c0001t0011g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1269+38A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129757 | ||||||
| chr3:154129793
|
T | A | 146 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1269+74T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129793 | ||||||
| chr3:154129796
|
T | C | 1 | a0002c0003t0006g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1269+77T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129796 | ||||||
| chr3:154129807
|
C | T | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1269+88C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129807 | ||||||
| chr3:154129817
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0029g0151 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1269+98G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129817 | ||||||
| chr3:154129880
|
T | C | 1 | a0002c0002t0008g0020 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1269+161T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154129880 | ||||||
| chr3:154130044
|
T | C | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+325T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130044 | ||||||
| chr3:154130046
|
C | T | 2 | a0002c0003t0005g0121a0002c0003t0006g0100 | 2 | NA18948.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1269+327C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130046 | ||||||
| chr3:154130068
|
C | T | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1269+349C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130068 | ||||||
| chr3:154130147
|
A | ATTTTTTT | 142 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(139): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1269+439_1269+445d others(9): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154130147 | |||||
| chr3:154130147
|
A | ATTTTTTT others(1): Show |
28 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(25): Show | 28 | HG00323.hp2 HG00438.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1269+438_1269+445d others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154130147 | |||||
| chr3:154130147
|
A | ATTTTTTT others(2): Show |
90 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(87): Show | 91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1269+437_1269+445d others(11): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154130147 | |||||
| chr3:154130147
|
A | ATTTTTTT others(3): Show |
6 | a0002c0002t0003g0079a0002c0002t0008g0080a0002c0002t0008g0081others(3): Show | 6 | HG01934.hp1 HG03579.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1269+436_1269+445d others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154130147 | |||||
| chr3:154130147
|
A | ATTTTTTT others(4): Show |
1 | a0002c0003t0005g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1269+435_1269+445d others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154130147 | |||||
| chr3:154130180
|
T | C | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+461T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130180 | ||||||
| chr3:154130241
|
T | C | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+522T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130241 | ||||||
| chr3:154130431
|
G | A | 9 | a0002c0003t0003g0098a0002c0003t0005g0135a0002c0003t0006g0096others(6): Show | 9 | HG01433.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1269+712G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130431 | ||||||
| chr3:154130619
|
T | C | 1 | a0002c0002t0005g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1269+900T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130619 | ||||||
| chr3:154130821
|
G | A | 2 | a0001c0001t0007g0144a0001c0015t0002g0143 | 2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1269+1102G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154130821 | ||||||
| chr3:154131000
|
A | G | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1269+1281A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131000 | ||||||
| chr3:154131011
|
G | A | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1269+1292G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131011 | ||||||
| chr3:154131087
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1269+1368T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131087 | ||||||
| chr3:154131169
|
A | C | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1269+1450A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131169 | ||||||
| chr3:154131182
|
T | C | 1 | a0002c0003t0005g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1269+1463T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131182 | ||||||
| chr3:154131298
|
G | A | 1 | a0002c0003t0003g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1269+1579G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131298 | ||||||
| chr3:154131450
|
C | T | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1269+1731C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131450 | ||||||
| chr3:154131486
|
C | T | 1 | a0001c0001t0043g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1269+1767C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131486 | ||||||
| chr3:154131884
|
A | G | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1269+2165A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154131884 | ||||||
| chr3:154132077
|
A | C | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+2358A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154132077 | ||||||
| chr3:154132738
|
T | C | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1269+3019T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154132738 | ||||||
| chr3:154132908
|
C | T | 2 | a0002c0002t0028g0077a0002c0002t0028g0078 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1269+3189C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154132908 | ||||||
| chr3:154132994
|
G | A | 1 | a0002c0003t0006g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1269+3275G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154132994 | ||||||
| chr3:154133272
|
A | G | 107 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(104): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1269+3553A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154133272 | ||||||
| chr3:154133592
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1269+3873A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154133592 | ||||||
| chr3:154133691
|
T | C | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1269+3972T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154133691 | ||||||
| chr3:154133746
|
C | G | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+4027C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154133746 | ||||||
| chr3:154134042
|
C | G | 1 | a0001c0001t0002g0247 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1269+4323C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134042 | ||||||
| chr3:154134074
|
T | A | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1269+4355T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134074 | ||||||
| chr3:154134275
|
A | T | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1269+4556A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134275 | ||||||
| chr3:154134366
|
CA | C | 4 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273others(1): Show | 4 | NA18946.hp1 NA18948.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+4649delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154134366 | |||||
| chr3:154134466
|
A | G | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1269+4747A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134466 | ||||||
| chr3:154134470
|
C | T | 1 | a0002c0003t0005g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1269+4751C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134470 | ||||||
| chr3:154134653
|
T | C | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+4934T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134653 | ||||||
| chr3:154134687
|
A | G | 69 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(66): Show | 69 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.1269+4968A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134687 | ||||||
| chr3:154134771
|
GT | G | 10 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1269+5063delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154134771 | |||||
| chr3:154134794
|
A | G | 159 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1269+5075A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134794 | ||||||
| chr3:154134867
|
A | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1269+5148A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134867 | ||||||
| chr3:154134948
|
A | G | 1 | a0001c0001t0013g0246 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1269+5229A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154134948 | ||||||
| chr3:154135101
|
G | C | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+5382G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135101 | ||||||
| chr3:154135147
|
A | G | 1 | a0001c0001t0014g0277 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1269+5428A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135147 | ||||||
| chr3:154135155
|
T | C | 1 | a0003c0004t0040g0014 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1269+5436T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135155 | ||||||
| chr3:154135453
|
C | A | 1 | a0002c0002t0024g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1269+5734C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135453 | ||||||
| chr3:154135837
|
A | G | 1 | a0006c0013t0025g0019 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1269+6118A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135837 | ||||||
| chr3:154135862
|
C | T | 1 | a0002c0003t0027g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1269+6143C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135862 | ||||||
| chr3:154135880
|
A | C | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1269+6161A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135880 | ||||||
| chr3:154135916
|
C | G | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1269+6197C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154135916 | ||||||
| chr3:154136045
|
C | G | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1269+6326C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136045 | ||||||
| chr3:154136211
|
T | TTAAAGTA others(27): Show |
1 | a0001c0001t0004g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1269+6517_1269+655 others(38): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136211 | |||||
| chr3:154136211
|
T | TTAAAGTA others(27): Show |
35 | a0001c0001t0001g0234a0001c0001t0002g0142a0001c0001t0002g0152others(32): Show | 36 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1269+6525_1269+652 others(38): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136211 | |||||
| chr3:154136211
|
T | TTAAAGTA others(61): Show |
1 | a0001c0001t0004g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1269+6525_1269+652 others(72): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136211 | |||||
| chr3:154136232
|
T | C | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1269+6513T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136232 | ||||||
| chr3:154136245
|
C | CTAAAGTA others(61): Show |
3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1269+6550_1269+655 others(72): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136245 | |||||
| chr3:154136245
|
C | G | 4 | a0001c0001t0002g0224a0001c0001t0002g0245a0003c0004t0010g0013others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+6526C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136245 | ||||||
| chr3:154136245
|
CTAAAGTA others(27): Show |
C | 109 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(106): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1269+6551_1269+658 others(38): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136245 | |||||
| chr3:154136270
|
G | A | 168 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1269+6551G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136270 | ||||||
| chr3:154136279
|
G | C | 46 | a0001c0001t0001g0234a0001c0001t0002g0002a0001c0001t0002g0142others(43): Show | 47 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1269+6560G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136279 | ||||||
| chr3:154136279
|
G | GTAAAGTA others(27): Show |
107 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1269+6576_1269+660 others(38): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136279 | |||||
| chr3:154136279
|
G | GTAAAGTA others(61): Show |
4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1269+6609_1269+661 others(72): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154136279 | |||||
| chr3:154136343
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0033g0221 | 3 | HG03491.hp2 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1269+6624C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136343 | ||||||
| chr3:154136603
|
T | C | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1269+6884T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136603 | ||||||
| chr3:154136834
|
T | A | 157 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1269+7115T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136834 | ||||||
| chr3:154136898
|
T | C | 1 | a0001c0001t0012g0166 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1269+7179T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136898 | ||||||
| chr3:154136991
|
A | T | 2 | a0001c0001t0009g0244a0001c0001t0011g0270 | 2 | NA18954.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1269+7272A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136991 | ||||||
| chr3:154137060
|
C | T | 12 | a0002c0002t0003g0026a0002c0002t0003g0068a0002c0002t0003g0069others(9): Show | 12 | HG00558.hp2 HG02015.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.1269+7341C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137060 | ||||||
| chr3:154137072
|
G | A | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1269+7353G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137072 | ||||||
| chr3:154137286
|
C | T | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1269+7567C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137286 | ||||||
| chr3:154137462
|
G | T | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1269+7743G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137462 | ||||||
| chr3:154137618
|
C | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0262a0001c0001t0012g0263 | 4 | NA19004.hp2 NA19060.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1269+7899C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137618 | ||||||
| chr3:154137691
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1269+7972T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137691 | ||||||
| chr3:154137813
|
T | TA | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1269+8109dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154137813 | |||||
| chr3:154137829
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1269+8110G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154137829 | ||||||
| chr3:154138150
|
C | T | 2 | a0007c0006t0017g0128a0007c0006t0017g0129 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1269+8431C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154138150 | ||||||
| chr3:154138155
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0029g0151 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1269+8436G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154138155 | ||||||
| chr3:154138230
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1269+8511G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154138230 | ||||||
| chr3:154138242
|
A | AT | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+8530dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154138242 | |||||
| chr3:154138543
|
A | C | 102 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(99): Show | 103 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1269+8824A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154138543 | ||||||
| chr3:154138986
|
T | G | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1269+9267T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154138986 | ||||||
| chr3:154139115
|
A | G | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1269+9396A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139115 | ||||||
| chr3:154139181
|
T | C | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1269+9462T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139181 | ||||||
| chr3:154139512
|
G | C | 1 | a0001c0001t0002g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1269+9793G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139512 | ||||||
| chr3:154139558
|
A | G | 13 | a0002c0002t0003g0026a0002c0002t0003g0065a0002c0002t0003g0068others(10): Show | 13 | HG00558.hp2 HG02015.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1270-9831A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139558 | ||||||
| chr3:154139890
|
G | A | 52 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0173others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1270-9499G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139890 | ||||||
| chr3:154139907
|
G | A | 5 | a0001c0001t0002g0225a0001c0001t0002g0229a0001c0001t0009g0227others(2): Show | 5 | HG00738.hp2 HG01167.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270-9482G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154139907 | ||||||
| chr3:154140113
|
T | TC | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1270-9276_1270-927 others(5): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140113 | ||||||
| chr3:154140273
|
C | T | 2 | a0007c0006t0017g0128a0007c0006t0017g0129 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1270-9116C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140273 | ||||||
| chr3:154140337
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0002g0203 | 2 | HG00609.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1270-9052G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140337 | ||||||
| chr3:154140356
|
A | G | 1 | a0001c0001t0009g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1270-9033A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140356 | ||||||
| chr3:154140588
|
C | CT | 147 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1270-8785dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154140588 | |||||
| chr3:154140588
|
CT | C | 107 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(104): Show | 108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1270-8785delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154140588 | |||||
| chr3:154140609
|
T | C | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1270-8780T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140609 | ||||||
| chr3:154140683
|
C | T | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-8706C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140683 | ||||||
| chr3:154140684
|
G | C | 66 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0156others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1270-8705G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140684 | ||||||
| chr3:154140779
|
T | C | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1270-8610T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140779 | ||||||
| chr3:154140855
|
A | G | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1270-8534A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154140855 | ||||||
| chr3:154140969
|
A | AT | 156 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1270-8410dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154140969 | |||||
| chr3:154141014
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1270-8375T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141014 | ||||||
| chr3:154141127
|
G | A | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-8262G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141127 | ||||||
| chr3:154141168
|
T | G | 108 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1270-8221T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141168 | ||||||
| chr3:154141193
|
C | T | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-8196C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141193 | ||||||
| chr3:154141517
|
G | T | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1270-7872G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141517 | ||||||
| chr3:154141900
|
T | C | 31 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(28): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1270-7489T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141900 | ||||||
| chr3:154141993
|
A | G | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-7396A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154141993 | ||||||
| chr3:154142042
|
G | C | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270-7347G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142042 | ||||||
| chr3:154142072
|
A | G | 3 | a0002c0002t0003g0025a0002c0002t0003g0064a0002c0002t0008g0032 | 3 | NA18945.hp1 NA18965.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1270-7317A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142072 | ||||||
| chr3:154142101
|
G | C | 2 | a0001c0001t0001g0204a0001c0001t0002g0203 | 2 | HG00609.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1270-7288G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142101 | ||||||
| chr3:154142219
|
C | CTTT | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-7159_1270-715 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154142219 | |||||
| chr3:154142231
|
T | C | 104 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(101): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1270-7158T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142231 | ||||||
| chr3:154142695
|
T | C | 1 | a0001c0015t0002g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1270-6694T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142695 | ||||||
| chr3:154142863
|
C | T | 134 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1270-6526C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142863 | ||||||
| chr3:154142881
|
A | G | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-6508A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142881 | ||||||
| chr3:154142956
|
C | A | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1270-6433C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142956 | ||||||
| chr3:154142990
|
A | G | 104 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(101): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1270-6399A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154142990 | ||||||
| chr3:154143024
|
G | A | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-6365G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143024 | ||||||
| chr3:154143068
|
G | A | 108 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(105): Show | 109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1270-6321G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143068 | ||||||
| chr3:154143302
|
T | A | 5 | a0001c0001t0004g0171a0001c0001t0004g0219a0001c0001t0004g0250others(2): Show | 6 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270-6087T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143302 | ||||||
| chr3:154143412
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1270-5977A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143412 | ||||||
| chr3:154143534
|
A | T | 1 | a0001c0001t0012g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1270-5855A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143534 | ||||||
| chr3:154143839
|
T | G | 4 | a0002c0002t0003g0022a0002c0002t0003g0037a0002c0002t0003g0038others(1): Show | 4 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-5550T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143839 | ||||||
| chr3:154143958
|
C | A | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-5431C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154143958 | ||||||
| chr3:154144002
|
G | A | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-5387G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144002 | ||||||
| chr3:154144037
|
C | A | 1 | a0001c0001t0007g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1270-5352C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144037 | ||||||
| chr3:154144082
|
A | T | 1 | a0002c0002t0006g0063 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1270-5307A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144082 | ||||||
| chr3:154144134
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1270-5255G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144134 | ||||||
| chr3:154144140
|
G | A | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-5249G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144140 | ||||||
| chr3:154144307
|
T | C | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-5082T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144307 | ||||||
| chr3:154144323
|
T | G | 1 | a0002c0002t0003g0039 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1270-5066T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144323 | ||||||
| chr3:154144327
|
A | G | 1 | a0001c0001t0034g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1270-5062A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144327 | ||||||
| chr3:154144433
|
G | T | 3 | a0001c0001t0002g0142a0001c0001t0007g0144a0001c0015t0002g0143 | 3 | HG02602.hp1 HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1270-4956G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144433 | ||||||
| chr3:154144512
|
A | G | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-4877A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144512 | ||||||
| chr3:154144527
|
C | T | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1270-4862C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144527 | ||||||
| chr3:154144532
|
A | G | 104 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(101): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1270-4857A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144532 | ||||||
| chr3:154144782
|
A | G | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-4607A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144782 | ||||||
| chr3:154144830
|
G | A | 1 | a0002c0002t0003g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1270-4559G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144830 | ||||||
| chr3:154144930
|
C | T | 104 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(101): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1270-4459C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144930 | ||||||
| chr3:154144955
|
A | C | 14 | a0001c0001t0002g0142a0001c0001t0002g0152a0001c0001t0002g0240others(11): Show | 14 | HG01346.hp2 HG01358.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1270-4434A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144955 | ||||||
| chr3:154144956
|
A | C | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-4433A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144956 | ||||||
| chr3:154144958
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | NA18986.hp1 NA19001.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1270-4431C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144958 | ||||||
| chr3:154144968
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1270-4421C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154144968 | ||||||
| chr3:154145032
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1270-4357T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145032 | ||||||
| chr3:154145241
|
A | G | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270-4148A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145241 | ||||||
| chr3:154145402
|
C | T | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-3987C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145402 | ||||||
| chr3:154145624
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1270-3765A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145624 | ||||||
| chr3:154145640
|
C | T | 2 | a0002c0002t0003g0076a0002c0002t0008g0081 | 2 | NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1270-3749C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145640 | ||||||
| chr3:154145653
|
C | T | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1270-3736C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145653 | ||||||
| chr3:154145716
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1270-3673A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145716 | ||||||
| chr3:154145909
|
A | T | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-3480A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145909 | ||||||
| chr3:154145995
|
G | T | 71 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1270-3394G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145995 | ||||||
| chr3:154146022
|
G | A | 2 | a0001c0009t0022g0163a0001c0009t0022g0164 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1270-3367G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146022 | ||||||
| chr3:154146023
|
A | AATACTCT others(17): Show |
2 | a0001c0009t0022g0163a0001c0009t0022g0164 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1270-3366_1270-336 others(28): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146023 | ||||||
| chr3:154146024
|
G | A | 2 | a0001c0009t0022g0163a0001c0009t0022g0164 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1270-3365G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146024 | ||||||
| chr3:154146082
|
G | A | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-3307G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146082 | ||||||
| chr3:154146084
|
A | G | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-3305A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146084 | ||||||
| chr3:154146211
|
C | T | 104 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(101): Show | 105 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1270-3178C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146211 | ||||||
| chr3:154146272
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1270-3117G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146272 | ||||||
| chr3:154146286
|
T | C | 20 | a0002c0003t0003g0106a0002c0003t0005g0001a0002c0003t0005g0107others(17): Show | 21 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.1270-3103T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146286 | ||||||
| chr3:154146426
|
C | CTAA | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1270-2961_1270-295 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154146426 | |||||
| chr3:154146507
|
C | T | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-2882C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146507 | ||||||
| chr3:154146528
|
A | T | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-2861A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146528 | ||||||
| chr3:154146582
|
G | A | 1 | a0002c0014t0019g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1270-2807G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146582 | ||||||
| chr3:154146685
|
A | G | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-2704A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146685 | ||||||
| chr3:154146721
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1270-2668T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154146721 | ||||||
| chr3:154147020
|
T | G | 2 | a0001c0001t0010g0239a0001c0001t0013g0246 | 2 | HG01346.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1270-2369T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147020 | ||||||
| chr3:154147026
|
G | A | 71 | a0002c0002t0003g0022a0002c0002t0003g0023a0002c0002t0003g0024others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1270-2363G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147026 | ||||||
| chr3:154147325
|
C | T | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-2064C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147325 | ||||||
| chr3:154147404
|
C | T | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-1985C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147404 | ||||||
| chr3:154147420
|
A | G | 1 | a0002c0003t0048g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1270-1969A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147420 | ||||||
| chr3:154147442
|
T | C | 2 | a0007c0006t0017g0128a0007c0006t0017g0129 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1270-1947T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147442 | ||||||
| chr3:154147613
|
C | G | 276 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(273): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1270-1776C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147613 | ||||||
| chr3:154147764
|
C | T | 1 | a0001c0001t0007g0160 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1270-1625C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154147764 | ||||||
| chr3:154148389
|
G | A | 1 | a0002c0003t0005g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1270-1000G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148389 | ||||||
| chr3:154148559
|
T | A | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1270-830T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148559 | ||||||
| chr3:154148670
|
A | G | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1270-719A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148670 | ||||||
| chr3:154148685
|
G | T | 1 | a0001c0015t0002g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1270-704G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148685 | ||||||
| chr3:154148803
|
T | G | 1 | a0001c0001t0002g0247 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1270-586T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148803 | ||||||
| chr3:154148918
|
A | T | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-471A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154148918 | ||||||
| chr3:154149174
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1270-215A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154149174 | ||||||
| chr3:154149202
|
C | T | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1270-187C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154149202 | ||||||
| chr3:154149247
|
AAATT | A | 260 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(257): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1270-138_1270-135d others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr3 | 154149247 | |||||
| chr3:154149474
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1326+29A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154149474 | ||||||
| chr3:154149783
|
G | A | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1326+338G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154149783 | ||||||
| chr3:154149925
|
T | TAA | 65 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(62): Show | 65 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.1326+493_1326+494d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 154149925 | |||||
| chr3:154149925
|
T | TAAA | 6 | a0002c0002t0003g0037a0002c0002t0005g0034a0002c0002t0005g0042others(3): Show | 6 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326+492_1326+494d others(5): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 154149925 | |||||
| chr3:154149938
|
A | T | 37 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(34): Show | 38 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1326+493A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154149938 | ||||||
| chr3:154150058
|
T | TTG | 5 | a0001c0001t0002g0224a0001c0001t0002g0226a0001c0001t0002g0238others(2): Show | 5 | HG00621.hp2 HG00735.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326+635_1326+636d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 154150058 | |||||
| chr3:154150058
|
TTG | T | 110 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(107): Show | 111 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1326+635_1326+636d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 154150058 | |||||
| chr3:154150113
|
T | C | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1326+668T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154150113 | ||||||
| chr3:154150137
|
C | CT | 254 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(251): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1326+706dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr3 | 154150137 | |||||
| chr3:154150325
|
G | A | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1326+880G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154150325 | ||||||
| chr3:154150377
|
A | G | 152 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1326+932A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154150377 | ||||||
| chr3:154150823
|
A | T | 12 | a0002c0002t0003g0039a0002c0002t0003g0057a0002c0002t0003g0061others(9): Show | 12 | HG00597.hp1 HG01496.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326+1378A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154150823 | ||||||
| chr3:154151353
|
A | G | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1327-1419A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151353 | ||||||
| chr3:154151580
|
C | T | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1327-1192C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151580 | ||||||
| chr3:154151587
|
C | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0012g0196others(1): Show | 4 | HG00741.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1185C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151587 | ||||||
| chr3:154151620
|
C | G | 1 | a0002c0003t0006g0117 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1327-1152C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151620 | ||||||
| chr3:154151641
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1327-1131A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151641 | ||||||
| chr3:154151681
|
C | T | 1 | a0001c0001t0004g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1327-1091C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151681 | ||||||
| chr3:154151684
|
A | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0012g0196others(1): Show | 4 | HG00741.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327-1088A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151684 | ||||||
| chr3:154151849
|
G | C | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1327-923G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151849 | ||||||
| chr3:154151934
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1327-838C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154151934 | ||||||
| chr3:154152305
|
C | T | 1 | a0002c0002t0003g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1327-467C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152305 | ||||||
| chr3:154152463
|
C | T | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1327-309C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152463 | ||||||
| chr3:154152500
|
G | C | 1 | a0002c0002t0003g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1327-272G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152500 | ||||||
| chr3:154152520
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0004g0208 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1327-252G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152520 | ||||||
| chr3:154152610
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0002g0203a0002c0003t0025g0105 | 3 | HG00609.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1327-162G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152610 | ||||||
| chr3:154152618
|
G | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1327-154G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152618 | ||||||
| chr3:154152722
|
G | A | 152 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1327-50G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152722 | ||||||
| chr3:154152725
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1327-47C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152725 | ||||||
| chr3:154152768
|
C | T | 1 | a0002c0002t0008g0032 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.1327-4C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152768 | ||||||
| chr3:154153094
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+162A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153094 | ||||||
| chr3:154153167
|
C | G | 35 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(32): Show | 36 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1487+235C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153167 | ||||||
| chr3:154153169
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1487+237A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153169 | ||||||
| chr3:154153208
|
T | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+276T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153208 | ||||||
| chr3:154153473
|
G | C | 3 | a0001c0001t0001g0153a0001c0001t0004g0155a0001c0001t0016g0154 | 3 | HG01891.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1487+541G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153473 | ||||||
| chr3:154153483
|
T | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+551T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153483 | ||||||
| chr3:154153597
|
A | G | 1 | a0001c0001t0011g0270 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1487+665A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153597 | ||||||
| chr3:154153603
|
G | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+671G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153603 | ||||||
| chr3:154153736
|
G | A | 81 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(78): Show | 81 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.1487+804G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153736 | ||||||
| chr3:154153776
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+844C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153776 | ||||||
| chr3:154153789
|
A | T | 1 | a0001c0001t0004g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1487+857A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153789 | ||||||
| chr3:154153794
|
T | C | 8 | a0002c0003t0005g0001a0002c0003t0005g0107a0002c0003t0005g0108others(5): Show | 9 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1487+862T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154153794 | ||||||
| chr3:154154154
|
A | G | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1487+1222A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154154 | ||||||
| chr3:154154556
|
A | G | 233 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1487+1624A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154556 | ||||||
| chr3:154154573
|
TATAG | T | 145 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(142): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1487+1645_1487+164 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154154573 | |||||
| chr3:154154643
|
G | A | 31 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(28): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1487+1711G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154643 | ||||||
| chr3:154154656
|
T | C | 233 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1487+1724T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154656 | ||||||
| chr3:154154854
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1487+1922C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154854 | ||||||
| chr3:154155031
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1487+2099C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155031 | ||||||
| chr3:154155044
|
A | G | 81 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(78): Show | 81 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.1487+2112A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155044 | ||||||
| chr3:154155339
|
C | T | 1 | a0004c0005t0013g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1487+2407C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155339 | ||||||
| chr3:154155349
|
C | G | 5 | a0001c0001t0001g0130a0001c0001t0017g0132a0001c0001t0021g0133others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1487+2417C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155349 | ||||||
| chr3:154155356
|
A | G | 81 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(78): Show | 81 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.1487+2424A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155356 | ||||||
| chr3:154155573
|
A | G | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1487+2641A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155573 | ||||||
| chr3:154155599
|
G | A | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1487+2667G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155599 | ||||||
| chr3:154155694
|
A | G | 1 | a0001c0001t0017g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1487+2762A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155694 | ||||||
| chr3:154155705
|
C | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1487+2773C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155705 | ||||||
| chr3:154155749
|
CAAAAG | C | 152 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1487+2818_1487+282 others(9): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155749 | ||||||
| chr3:154155785
|
A | G | 81 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(78): Show | 81 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.1487+2853A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155785 | ||||||
| chr3:154155795
|
A | G | 1 | a0001c0001t0007g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1487+2863A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155795 | ||||||
| chr3:154155854
|
T | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+2922T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154155854 | ||||||
| chr3:154156015
|
G | T | 1 | a0001c0001t0002g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1487+3083G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156015 | ||||||
| chr3:154156201
|
T | C | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1487+3269T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156201 | ||||||
| chr3:154156240
|
T | C | 4 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273others(1): Show | 4 | NA18946.hp1 NA18948.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487+3308T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156240 | ||||||
| chr3:154156350
|
C | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+3418C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156350 | ||||||
| chr3:154156572
|
C | G | 1 | a0001c0001t0004g0168 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1487+3640C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156572 | ||||||
| chr3:154156777
|
G | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+3845G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156777 | ||||||
| chr3:154156863
|
GTTAAGTA others(5): Show |
G | 2 | a0001c0001t0001g0195a0001c0001t0004g0193 | 2 | NA18953.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1487+3933_1487+394 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154156863 | |||||
| chr3:154156928
|
A | G | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1487+3996A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156928 | ||||||
| chr3:154156957
|
C | T | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+4025C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154156957 | ||||||
| chr3:154157076
|
A | G | 1 | a0002c0003t0005g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1487+4144A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157076 | ||||||
| chr3:154157167
|
TAAAACA | T | 65 | a0001c0001t0001g0146a0001c0001t0001g0204a0001c0001t0001g0207others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1487+4236_1487+424 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157167 | ||||||
| chr3:154157286
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+4354A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157286 | ||||||
| chr3:154157424
|
C | T | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1487+4492C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157424 | ||||||
| chr3:154157487
|
A | G | 31 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(28): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1487+4555A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157487 | ||||||
| chr3:154157571
|
A | C | 31 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(28): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1487+4639A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157571 | ||||||
| chr3:154157840
|
A | G | 33 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(30): Show | 34 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1487+4908A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157840 | ||||||
| chr3:154157924
|
T | C | 233 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1487+4992T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154157924 | ||||||
| chr3:154158002
|
C | T | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1487+5070C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158002 | ||||||
| chr3:154158087
|
T | G | 33 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(30): Show | 34 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1487+5155T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158087 | ||||||
| chr3:154158107
|
G | A | 1 | a0002c0003t0005g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1487+5175G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158107 | ||||||
| chr3:154158150
|
C | T | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1487+5218C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158150 | ||||||
| chr3:154158260
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1487+5328A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158260 | ||||||
| chr3:154158295
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0011g0002 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1487+5363T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158295 | ||||||
| chr3:154158312
|
G | A | 1 | a0011c0018t0007g0006 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1487+5380G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158312 | ||||||
| chr3:154158525
|
T | G | 31 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(28): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1487+5593T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158525 | ||||||
| chr3:154158590
|
A | G | 81 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(78): Show | 81 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.1487+5658A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158590 | ||||||
| chr3:154158614
|
A | G | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1487+5682A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158614 | ||||||
| chr3:154158659
|
C | T | 2 | a0002c0003t0005g0120a0002c0003t0006g0115 | 2 | HG02056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1487+5727C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154158659 | ||||||
| chr3:154158795
|
AT | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+5872delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154158795 | |||||
| chr3:154159032
|
C | T | 1 | a0002c0003t0048g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1487+6100C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159032 | ||||||
| chr3:154159037
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+6105A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159037 | ||||||
| chr3:154159084
|
T | G | 5 | a0001c0001t0002g0225a0001c0001t0002g0229a0001c0001t0009g0227others(2): Show | 5 | HG00738.hp2 HG01167.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487+6152T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159084 | ||||||
| chr3:154159140
|
G | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+6208G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159140 | ||||||
| chr3:154159372
|
G | A | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1487+6440G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159372 | ||||||
| chr3:154159526
|
C | T | 1 | a0001c0001t0043g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1487+6594C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159526 | ||||||
| chr3:154159527
|
C | A | 152 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1487+6595C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159527 | ||||||
| chr3:154159530
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1487+6598G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154159530 | ||||||
| chr3:154160126
|
T | A | 33 | a0002c0003t0003g0089a0002c0003t0003g0106a0002c0003t0004g0085others(30): Show | 34 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1487+7194T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160126 | ||||||
| chr3:154160285
|
A | G | 10 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7353A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160285 | ||||||
| chr3:154160287
|
G | T | 1 | a0001c0001t0002g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1487+7355G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160287 | ||||||
| chr3:154160404
|
T | C | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1487+7472T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160404 | ||||||
| chr3:154160491
|
G | A | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1487+7559G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160491 | ||||||
| chr3:154160703
|
A | C | 1 | a0001c0001t0014g0277 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1487+7771A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154160703 | ||||||
| chr3:154161021
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1487+8089A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161021 | ||||||
| chr3:154161029
|
C | T | 1 | a0001c0001t0010g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1487+8097C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161029 | ||||||
| chr3:154161098
|
GT | G | 6 | a0002c0003t0005g0114a0002c0003t0005g0119a0002c0003t0005g0121others(3): Show | 6 | HG00544.hp1 NA18948.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487+8169delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161098 | |||||
| chr3:154161098
|
GTTTGT | G | 10 | a0002c0003t0005g0001a0002c0003t0005g0107a0002c0003t0005g0108others(7): Show | 11 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.1487+8167_1487+817 others(9): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161098 | ||||||
| chr3:154161098
|
GTTTGTGT others(4): Show |
G | 4 | a0002c0003t0004g0085a0002c0003t0004g0086a0007c0006t0017g0128others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+8167_1487+817 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161098 | ||||||
| chr3:154161098
|
GTTTGTGT others(6): Show |
G | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1487+8167_1487+817 others(17): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161098 | ||||||
| chr3:154161099
|
TTTG | T | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1487+8169_1487+817 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTG | T | 5 | a0001c0001t0002g0249a0001c0001t0004g0149a0001c0001t0007g0206others(2): Show | 5 | HG00621.hp2 HG01255.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487+8169_1487+817 others(9): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG | T | 40 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0207others(37): Show | 42 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.1487+8169_1487+817 others(11): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG others(2): Show |
T | 89 | a0001c0001t0001g0150a0001c0001t0001g0173a0001c0001t0001g0174others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1487+8169_1487+817 others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG others(4): Show |
T | 1 | a0002c0002t0024g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1487+8169_1487+817 others(15): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG others(6): Show |
T | 14 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.1487+8169_1487+818 others(17): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG others(8): Show |
T | 8 | a0002c0002t0019g0056a0002c0003t0018g0092a0002c0003t0044g0094others(5): Show | 8 | HG02055.hp1 HG03195.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1487+8169_1487+818 others(19): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161099
|
TTTGTGTG others(10): Show |
T | 73 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1487+8169_1487+818 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161099 | |||||
| chr3:154161100
|
T | G | 13 | a0002c0003t0003g0106a0002c0003t0005g0114a0002c0003t0005g0116others(10): Show | 13 | HG00544.hp1 HG00609.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1487+8168T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161100 | ||||||
| chr3:154161111
|
T | G | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1487+8179T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161111 | ||||||
| chr3:154161205
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1487+8273A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161205 | ||||||
| chr3:154161312
|
C | CAAATATA others(9): Show |
266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+8382_1487+838 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154161312 | |||||
| chr3:154161330
|
G | A | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1487+8398G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161330 | ||||||
| chr3:154161678
|
G | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+8746G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154161678 | ||||||
| chr3:154162181
|
A | G | 1 | a0002c0002t0005g0060 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1487+9249A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162181 | ||||||
| chr3:154162298
|
G | T | 1 | a0002c0002t0005g0060 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1487+9366G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162298 | ||||||
| chr3:154162437
|
T | G | 1 | a0001c0001t0020g0003 | 2 | HG00140.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1487+9505T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162437 | ||||||
| chr3:154162531
|
G | A | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1487+9599G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162531 | ||||||
| chr3:154162596
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0017g0132a0001c0001t0023g0131 | 3 | HG01891.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1487+9664T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162596 | ||||||
| chr3:154162670
|
G | A | 1 | a0001c0001t0002g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1487+9738G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162670 | ||||||
| chr3:154162772
|
C | T | 2 | a0005c0008t0014g0122a0005c0008t0023g0123 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1487+9840C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162772 | ||||||
| chr3:154162786
|
G | T | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1487+9854G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162786 | ||||||
| chr3:154162819
|
TG | T | 3 | a0001c0001t0001g0180a0001c0001t0002g0224a0001c0001t0002g0238 | 3 | HG00735.hp1 HG00735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1487+9890delG | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154162819 | |||||
| chr3:154162895
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1487+9963C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162895 | ||||||
| chr3:154162907
|
C | T | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1487+9975C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162907 | ||||||
| chr3:154162935
|
C | T | 150 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(147): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1487+10003C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162935 | ||||||
| chr3:154162966
|
G | A | 1 | a0002c0002t0003g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1487+10034G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154162966 | ||||||
| chr3:154163072
|
C | G | 1 | a0001c0001t0015g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1487+10140C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163072 | ||||||
| chr3:154163093
|
T | G | 2 | a0002c0003t0005g0121a0002c0003t0006g0100 | 2 | NA18948.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1487+10161T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163093 | ||||||
| chr3:154163115
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1487+10183A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163115 | ||||||
| chr3:154163192
|
A | G | 6 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(3): Show | 6 | HG03195.hp1 HG03453.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1487+10260A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163192 | ||||||
| chr3:154163439
|
A | G | 1 | a0001c0001t0014g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1487+10507A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163439 | ||||||
| chr3:154163483
|
G | A | 4 | a0002c0002t0005g0034a0002c0002t0005g0042a0002c0002t0005g0043others(1): Show | 4 | HG01243.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487+10551G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163483 | ||||||
| chr3:154163742
|
C | A | 1 | a0001c0001t0001g0194 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1487+10810C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163742 | ||||||
| chr3:154163758
|
G | A | 3 | a0001c0001t0021g0133a0005c0008t0014g0122a0005c0008t0023g0123 | 3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1487+10826G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154163758 | ||||||
| chr3:154163917
|
GCTGT | G | 3 | a0001c0001t0017g0132a0007c0006t0017g0128a0007c0006t0017g0129 | 3 | HG01884.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1487+10988_1487+10 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154163917 | |||||
| chr3:154164047
|
G | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+11115G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164047 | ||||||
| chr3:154164095
|
T | C | 1 | a0001c0001t0012g0166 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1487+11163T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164095 | ||||||
| chr3:154164097
|
G | A | 2 | a0002c0007t0018g0090a0002c0007t0018g0091 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1487+11165G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164097 | ||||||
| chr3:154164139
|
T | A | 3 | a0001c0001t0017g0132a0007c0006t0017g0128a0007c0006t0017g0129 | 3 | HG01884.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1487+11207T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164139 | ||||||
| chr3:154164177
|
C | T | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0012g0263others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1487+11245C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164177 | ||||||
| chr3:154164219
|
T | C | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0012g0263others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1487+11287T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164219 | ||||||
| chr3:154164405
|
T | C | 1 | a0001c0001t0004g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1487+11473T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164405 | ||||||
| chr3:154164456
|
T | TTATC | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+11527_1487+11 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154164456 | |||||
| chr3:154164482
|
A | G | 1 | a0002c0003t0004g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1487+11550A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164482 | ||||||
| chr3:154164577
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0033g0221 | 3 | HG03491.hp2 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1487+11645G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164577 | ||||||
| chr3:154164852
|
T | G | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0012g0263others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1487+11920T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154164852 | ||||||
| chr3:154165076
|
G | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+12144G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165076 | ||||||
| chr3:154165433
|
A | G | 3 | a0001c0001t0021g0133a0005c0008t0014g0122a0005c0008t0023g0123 | 3 | HG02055.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1487+12501A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165433 | ||||||
| chr3:154165496
|
C | T | 1 | a0001c0001t0007g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1487+12564C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165496 | ||||||
| chr3:154165516
|
A | G | 4 | a0001c0001t0007g0274a0001c0001t0014g0276a0001c0001t0014g0277others(1): Show | 4 | HG02258.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+12584A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165516 | ||||||
| chr3:154165555
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+12623C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165555 | ||||||
| chr3:154165606
|
C | T | 1 | a0002c0003t0005g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1487+12674C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165606 | ||||||
| chr3:154165637
|
C | A | 179 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1487+12705C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165637 | ||||||
| chr3:154165649
|
A | T | 1 | a0002c0014t0019g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1487+12717A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165649 | ||||||
| chr3:154165734
|
A | G | 3 | a0002c0002t0003g0025a0002c0002t0003g0064a0002c0002t0008g0032 | 3 | NA18945.hp1 NA18965.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1487+12802A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165734 | ||||||
| chr3:154165753
|
G | T | 1 | a0002c0003t0005g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1487+12821G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165753 | ||||||
| chr3:154165841
|
G | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0179 | 2 | NA18942.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1487+12909G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165841 | ||||||
| chr3:154165876
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1487+12944A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165876 | ||||||
| chr3:154165957
|
C | G | 71 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(68): Show | 71 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.1487+13025C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154165957 | ||||||
| chr3:154166145
|
G | A | 7 | a0001c0001t0002g0226a0001c0001t0002g0233a0001c0001t0002g0247others(4): Show | 7 | NA18945.hp2 NA18946.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1487+13213G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166145 | ||||||
| chr3:154166172
|
A | G | 1 | a0005c0008t0023g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1487+13240A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166172 | ||||||
| chr3:154166485
|
G | A | 4 | a0002c0002t0051g0033a0002c0003t0025g0105a0002c0007t0018g0090others(1): Show | 4 | HG03041.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+13553G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166485 | ||||||
| chr3:154166516
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1487+13584C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166516 | ||||||
| chr3:154166551
|
G | C | 1 | a0001c0001t0007g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1487+13619G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166551 | ||||||
| chr3:154166728
|
T | A | 174 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1487+13796T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166728 | ||||||
| chr3:154166994
|
A | G | 3 | a0001c0001t0017g0132a0007c0006t0017g0128a0007c0006t0017g0129 | 3 | HG01884.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1487+14062A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154166994 | ||||||
| chr3:154167004
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1487+14072C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167004 | ||||||
| chr3:154167029
|
A | G | 1 | a0002c0002t0003g0025 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1487+14097A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167029 | ||||||
| chr3:154167124
|
T | G | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1487+14192T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167124 | ||||||
| chr3:154167217
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+14285A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167217 | ||||||
| chr3:154167410
|
G | C | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1487+14478G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167410 | ||||||
| chr3:154167484
|
T | C | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1487+14552T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167484 | ||||||
| chr3:154167671
|
A | T | 1 | a0002c0002t0049g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1487+14739A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167671 | ||||||
| chr3:154167714
|
T | C | 134 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(131): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1487+14782T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167714 | ||||||
| chr3:154167831
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1487+14899T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167831 | ||||||
| chr3:154168319
|
A | G | 1 | a0001c0001t0010g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1487+15387A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168319 | ||||||
| chr3:154168524
|
C | G | 1 | a0002c0002t0024g0062 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1487+15592C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168524 | ||||||
| chr3:154168529
|
A | G | 130 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(127): Show | 130 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.1487+15597A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168529 | ||||||
| chr3:154168661
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0234a0001c0001t0004g0145 | 3 | HG00735.hp1 HG01168.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1487+15729G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168661 | ||||||
| chr3:154168796
|
G | A | 1 | a0002c0003t0006g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1487+15864G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168796 | ||||||
| chr3:154168812
|
C | A | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1487+15880C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168812 | ||||||
| chr3:154168883
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1487+15951C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168883 | ||||||
| chr3:154168908
|
TAGATC | T | 134 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(131): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1487+15980_1487+15 others(11): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154168908 | |||||
| chr3:154168970
|
C | T | 1 | a0002c0003t0050g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1487+16038C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154168970 | ||||||
| chr3:154168986
|
G | GA | 7 | a0001c0001t0004g0257a0001c0001t0004g0266a0001c0001t0017g0132others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1487+16064dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154168986 | |||||
| chr3:154169018
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0023g0131a0001c0001t0043g0134others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487+16086G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169018 | ||||||
| chr3:154169120
|
G | A | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1487+16188G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169120 | ||||||
| chr3:154169202
|
A | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1487+16270A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169202 | ||||||
| chr3:154169225
|
T | G | 66 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(63): Show | 66 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.1487+16293T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169225 | ||||||
| chr3:154169269
|
C | T | 1 | a0002c0002t0003g0054 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1487+16337C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169269 | ||||||
| chr3:154169270
|
G | A | 4 | a0001c0001t0010g0140a0001c0001t0011g0141a0003c0004t0010g0013others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1487+16338G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169270 | ||||||
| chr3:154169390
|
T | C | 73 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0015g0124others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1487+16458T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169390 | ||||||
| chr3:154169654
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1487+16722T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169654 | ||||||
| chr3:154169877
|
C | T | 133 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1487+16945C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169877 | ||||||
| chr3:154169975
|
G | A | 133 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1487+17043G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154169975 | ||||||
| chr3:154170140
|
T | C | 2 | a0002c0002t0028g0077a0002c0002t0028g0078 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1487+17208T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154170140 | ||||||
| chr3:154171175
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1488-16510G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171175 | ||||||
| chr3:154171177
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1488-16508C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171177 | ||||||
| chr3:154171183
|
A | G | 1 | a0001c0001t0004g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1488-16502A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171183 | ||||||
| chr3:154171618
|
A | G | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1488-16067A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171618 | ||||||
| chr3:154171709
|
C | T | 3 | a0002c0002t0006g0027a0002c0002t0006g0029a0002c0002t0006g0063 | 3 | NA18946.hp2 NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1488-15976C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171709 | ||||||
| chr3:154171812
|
T | A | 135 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1488-15873T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171812 | ||||||
| chr3:154171836
|
G | C | 133 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1488-15849G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171836 | ||||||
| chr3:154171863
|
G | T | 66 | a0001c0001t0007g0144a0001c0001t0007g0175a0002c0002t0003g0022others(63): Show | 66 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.1488-15822G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171863 | ||||||
| chr3:154171936
|
T | A | 9 | a0001c0001t0010g0140a0001c0001t0011g0141a0003c0004t0002g0007others(6): Show | 9 | HG00741.hp2 HG01081.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488-15749T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154171936 | ||||||
| chr3:154172066
|
T | C | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-15619T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172066 | ||||||
| chr3:154172067
|
G | A | 3 | a0002c0002t0006g0027a0002c0002t0006g0029a0002c0002t0006g0063 | 3 | NA18946.hp2 NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1488-15618G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172067 | ||||||
| chr3:154172117
|
A | G | 135 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1488-15568A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172117 | ||||||
| chr3:154172480
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1488-15205A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172480 | ||||||
| chr3:154172585
|
T | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-15100T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172585 | ||||||
| chr3:154172610
|
C | T | 1 | a0001c0001t0011g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1488-15075C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172610 | ||||||
| chr3:154172730
|
C | T | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1488-14955C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172730 | ||||||
| chr3:154172942
|
A | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0262a0001c0001t0012g0263 | 4 | NA19004.hp2 NA19060.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-14743A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154172942 | ||||||
| chr3:154173068
|
A | G | 1 | a0001c0001t0004g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1488-14617A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173068 | ||||||
| chr3:154173201
|
A | AC | 44 | a0001c0001t0001g0153a0001c0001t0001g0180a0001c0001t0001g0189others(41): Show | 44 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1488-14477dupC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154173201 | |||||
| chr3:154173392
|
C | G | 1 | a0001c0001t0004g0148 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1488-14293C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173392 | ||||||
| chr3:154173393
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-14292A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173393 | ||||||
| chr3:154173428
|
A | G | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1488-14257A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173428 | ||||||
| chr3:154173447
|
CAATT | C | 4 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0007t0018g0090others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-14232_1488-14 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154173447 | |||||
| chr3:154173456
|
A | C | 1 | a0001c0001t0002g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1488-14229A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173456 | ||||||
| chr3:154173689
|
C | T | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1488-13996C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173689 | ||||||
| chr3:154173700
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-13985A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173700 | ||||||
| chr3:154173701
|
T | C | 1 | a0002c0002t0047g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1488-13984T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173701 | ||||||
| chr3:154173830
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1488-13855A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173830 | ||||||
| chr3:154173833
|
A | G | 3 | a0004c0005t0013g0136a0004c0005t0013g0158a0004c0005t0013g0159 | 3 | HG01243.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1488-13852A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173833 | ||||||
| chr3:154173897
|
T | C | 131 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(128): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1488-13788T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173897 | ||||||
| chr3:154173916
|
TA | T | 131 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(128): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1488-13768delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173916 | ||||||
| chr3:154173941
|
A | G | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1488-13744A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173941 | ||||||
| chr3:154174122
|
A | G | 1 | a0002c0003t0005g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1488-13563A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174122 | ||||||
| chr3:154174344
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0023g0131a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1488-13341T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174344 | ||||||
| chr3:154174801
|
T | C | 4 | a0001c0001t0007g0274a0001c0001t0014g0276a0001c0001t0014g0277others(1): Show | 4 | HG02258.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-12884T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174801 | ||||||
| chr3:154174854
|
T | A | 1 | a0001c0001t0007g0182 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1488-12831T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174854 | ||||||
| chr3:154174907
|
A | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1488-12778A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174907 | ||||||
| chr3:154174928
|
A | G | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-12757A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154174928 | ||||||
| chr3:154175005
|
G | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1488-12680G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175005 | ||||||
| chr3:154175055
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-12630C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175055 | ||||||
| chr3:154175186
|
C | A | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-12499C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175186 | ||||||
| chr3:154175218
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1488-12467C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175218 | ||||||
| chr3:154175304
|
A | C | 8 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0003t0018g0092others(5): Show | 8 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-12381A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175304 | ||||||
| chr3:154175411
|
C | T | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1488-12274C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175411 | ||||||
| chr3:154175417
|
A | C | 67 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0156others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1488-12268A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175417 | ||||||
| chr3:154175433
|
TA | T | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1488-12242delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154175433 | |||||
| chr3:154175450
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1488-12235G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175450 | ||||||
| chr3:154175563
|
A | G | 206 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(203): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1488-12122A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175563 | ||||||
| chr3:154175754
|
T | C | 73 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1488-11931T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175754 | ||||||
| chr3:154175757
|
A | G | 24 | a0002c0002t0003g0025a0002c0002t0005g0060a0002c0003t0003g0089others(21): Show | 25 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1488-11928A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175757 | ||||||
| chr3:154175758
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-11927T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154175758 | ||||||
| chr3:154176199
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0004g0193 | 2 | NA18953.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1488-11486T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176199 | ||||||
| chr3:154176361
|
C | CT | 4 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0007t0018g0090others(1): Show | 4 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-11316dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154176361 | |||||
| chr3:154176448
|
T | C | 8 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0003t0018g0092others(5): Show | 8 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-11237T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176448 | ||||||
| chr3:154176546
|
A | G | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488-11139A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176546 | ||||||
| chr3:154176718
|
G | A | 73 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1488-10967G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176718 | ||||||
| chr3:154176737
|
A | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1488-10948A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176737 | ||||||
| chr3:154176760
|
G | A | 26 | a0002c0002t0003g0025a0002c0002t0005g0060a0002c0003t0003g0089others(23): Show | 27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1488-10925G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176760 | ||||||
| chr3:154176850
|
C | T | 85 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(82): Show | 85 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.1488-10835C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176850 | ||||||
| chr3:154176926
|
A | G | 1 | a0002c0003t0005g0113 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1488-10759A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176926 | ||||||
| chr3:154176937
|
C | T | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1488-10748C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154176937 | ||||||
| chr3:154177085
|
T | C | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1488-10600T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177085 | ||||||
| chr3:154177207
|
T | G | 73 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1488-10478T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177207 | ||||||
| chr3:154177358
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-10327C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177358 | ||||||
| chr3:154177374
|
A | G | 1 | a0002c0003t0005g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1488-10311A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177374 | ||||||
| chr3:154177502
|
G | A | 1 | a0003c0004t0002g0007 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1488-10183G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177502 | ||||||
| chr3:154177561
|
A | G | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488-10124A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154177561 | ||||||
| chr3:154178096
|
C | T | 73 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1488-9589C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178096 | ||||||
| chr3:154178097
|
G | A | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488-9588G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178097 | ||||||
| chr3:154178205
|
A | G | 4 | a0001c0001t0002g0142a0001c0015t0002g0143a0002c0002t0024g0035others(1): Show | 4 | HG02071.hp2 HG02735.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-9480A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178205 | ||||||
| chr3:154178333
|
C | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-9352C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178333 | ||||||
| chr3:154178393
|
G | A | 130 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1488-9292G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178393 | ||||||
| chr3:154178418
|
T | G | 2 | a0001c0009t0022g0163a0001c0009t0022g0164 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1488-9267T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178418 | ||||||
| chr3:154178614
|
C | T | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-9071C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154178614 | ||||||
| chr3:154179066
|
T | C | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1488-8619T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154179066 | ||||||
| chr3:154179516
|
A | G | 130 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1488-8169A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154179516 | ||||||
| chr3:154179519
|
G | A | 2 | a0002c0002t0024g0035a0002c0002t0024g0062 | 2 | HG02071.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1488-8166G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154179519 | ||||||
| chr3:154179531
|
C | CTA | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488-8153_1488-815 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154179531 | |||||
| chr3:154179755
|
A | G | 1 | a0003c0004t0031g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1488-7930A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154179755 | ||||||
| chr3:154179998
|
G | A | 12 | a0002c0002t0003g0026a0002c0002t0003g0068a0002c0002t0003g0069others(9): Show | 12 | HG00558.hp2 HG02015.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.1488-7687G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154179998 | ||||||
| chr3:154180453
|
T | C | 1 | a0001c0001t0007g0160 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1488-7232T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180453 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3163): Show |
4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3174): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3163): Show |
73 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(70): Show | 73 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3174): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3163): Show |
1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3174): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3163): Show |
1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3174): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
1 | a0001c0001t0009g0227 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
1 | a0001c0001t0009g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
7 | a0001c0001t0002g0226a0001c0001t0002g0233a0001c0001t0002g0247others(4): Show | 7 | NA18945.hp2 NA18946.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
35 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(32): Show | 35 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3166): Show |
2 | a0001c0001t0011g0243a0002c0002t0024g0035 | 2 | HG01175.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3177): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3161): Show |
1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3172): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
122 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0153others(119): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
1 | a0001c0001t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
1 | a0001c0001t0020g0003 | 2 | HG00140.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
3 | a0001c0001t0004g0139a0002c0003t0005g0135a0002c0003t0026g0103 | 3 | HG01109.hp2 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
1 | a0001c0001t0012g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3163): Show |
5 | a0002c0002t0051g0033a0002c0003t0018g0092a0002c0003t0044g0094others(2): Show | 5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3174): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3164): Show |
1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1488-7066_1488-706 others(3175): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180619
|
A | ACATTTTT others(3165): Show |
2 | a0001c0001t0010g0239a0001c0001t0013g0246 | 2 | HG01346.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1488-7066_1488-706 others(3176): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180619 | ||||||
| chr3:154180729
|
A | C | 204 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(201): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1488-6956A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180729 | ||||||
| chr3:154180771
|
A | G | 264 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1488-6914A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180771 | ||||||
| chr3:154180790
|
G | A | 3 | a0002c0002t0003g0025a0002c0003t0005g0120a0002c0003t0006g0115 | 3 | HG02056.hp1 NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1488-6895G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180790 | ||||||
| chr3:154180830
|
T | C | 8 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0003t0018g0092others(5): Show | 8 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-6855T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180830 | ||||||
| chr3:154180880
|
G | A | 83 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(80): Show | 83 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1488-6805G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154180880 | ||||||
| chr3:154181027
|
G | A | 1 | a0002c0003t0005g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1488-6658G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181027 | ||||||
| chr3:154181111
|
C | T | 1 | a0002c0002t0003g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1488-6574C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181111 | ||||||
| chr3:154181679
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1488-6006A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181679 | ||||||
| chr3:154181743
|
G | A | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1488-5942G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181743 | ||||||
| chr3:154181793
|
A | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488-5892A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181793 | ||||||
| chr3:154181902
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1488-5783C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181902 | ||||||
| chr3:154181920
|
T | C | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1488-5765T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181920 | ||||||
| chr3:154181961
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-5724G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181961 | ||||||
| chr3:154181994
|
TA | T | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-5690delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154181994 | ||||||
| chr3:154182072
|
A | T | 1 | a0001c0001t0014g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1488-5613A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182072 | ||||||
| chr3:154182131
|
C | T | 55 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0169others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.1488-5554C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182131 | ||||||
| chr3:154182331
|
A | G | 5 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488-5354A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182331 | ||||||
| chr3:154182337
|
G | A | 1 | a0002c0002t0028g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1488-5348G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182337 | ||||||
| chr3:154182552
|
A | C | 1 | a0001c0001t0007g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1488-5133A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182552 | ||||||
| chr3:154182576
|
A | G | 1 | a0001c0001t0012g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1488-5109A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182576 | ||||||
| chr3:154182623
|
A | G | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1488-5062A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182623 | ||||||
| chr3:154182677
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-5008T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182677 | ||||||
| chr3:154182787
|
G | A | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-4898G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154182787 | ||||||
| chr3:154183419
|
C | T | 1 | a0002c0002t0047g0041 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1488-4266C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183419 | ||||||
| chr3:154183453
|
C | T | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1488-4232C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183453 | ||||||
| chr3:154183545
|
G | A | 1 | a0002c0002t0003g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1488-4140G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183545 | ||||||
| chr3:154183765
|
A | G | 8 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0003t0018g0092others(5): Show | 8 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-3920A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183765 | ||||||
| chr3:154183883
|
A | T | 2 | a0001c0001t0004g0258a0001c0001t0012g0166 | 2 | HG00438.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1488-3802A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183883 | ||||||
| chr3:154183905
|
C | A | 278 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(275): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1488-3780C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154183905 | ||||||
| chr3:154183977
|
C | CTTTTTTT others(1): Show |
43 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(40): Show | 43 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1488-3702_1488-369 others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154183977 | |||||
| chr3:154183977
|
CT | C | 8 | a0001c0001t0037g0256a0002c0002t0051g0033a0002c0003t0018g0092others(5): Show | 8 | HG02145.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-3695delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154183977 | |||||
| chr3:154184004
|
G | A | 2 | a0002c0002t0003g0037a0002c0002t0008g0036 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1488-3681G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184004 | ||||||
| chr3:154184028
|
A | G | 74 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(71): Show | 74 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.1488-3657A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184028 | ||||||
| chr3:154184133
|
C | T | 1 | a0002c0002t0003g0051 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1488-3552C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184133 | ||||||
| chr3:154184197
|
C | T | 2 | a0001c0001t0007g0206a0002c0003t0003g0098 | 2 | HG01255.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1488-3488C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184197 | ||||||
| chr3:154184689
|
G | C | 8 | a0001c0001t0017g0132a0002c0002t0005g0034a0002c0002t0005g0042others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488-2996G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184689 | ||||||
| chr3:154184760
|
C | G | 2 | a0001c0001t0002g0002a0001c0001t0011g0002 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1488-2925C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184760 | ||||||
| chr3:154184995
|
A | G | 61 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1488-2690A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154184995 | ||||||
| chr3:154185056
|
G | A | 1 | a0001c0001t0041g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1488-2629G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185056 | ||||||
| chr3:154185079
|
A | G | 264 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1488-2606A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185079 | ||||||
| chr3:154185183
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0179 | 2 | NA18942.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1488-2502C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185183 | ||||||
| chr3:154185306
|
T | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1488-2379T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185306 | ||||||
| chr3:154185425
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-2260T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185425 | ||||||
| chr3:154185489
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1488-2196T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185489 | ||||||
| chr3:154185618
|
G | A | 98 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1488-2067G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185618 | ||||||
| chr3:154185747
|
A | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0235 | 2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1488-1938A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185747 | ||||||
| chr3:154185998
|
G | A | 61 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1488-1687G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154185998 | ||||||
| chr3:154186110
|
T | C | 1 | a0002c0002t0003g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1488-1575T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186110 | ||||||
| chr3:154186117
|
G | A | 3 | a0002c0002t0003g0039a0002c0002t0003g0057a0002c0002t0003g0084 | 3 | HG02165.hp1 NA18950.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1488-1568G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186117 | ||||||
| chr3:154186136
|
G | GAC | 3 | a0002c0002t0005g0042a0002c0002t0005g0043a0002c0003t0050g0099 | 3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1488-1520_1488-151 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACAC | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0014g0277others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1488-1522_1488-151 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACAC | 68 | a0001c0001t0001g0195a0001c0001t0001g0251a0001c0001t0002g0203others(65): Show | 68 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1488-1524_1488-151 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(1): Show |
91 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1488-1526_1488-151 others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(3): Show |
49 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0192others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1488-1528_1488-151 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(5): Show |
20 | a0001c0001t0001g0156a0001c0001t0001g0199a0001c0001t0002g0249others(17): Show | 21 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1488-1530_1488-151 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(7): Show |
8 | a0001c0001t0002g0142a0001c0001t0002g0236a0001c0001t0010g0239others(5): Show | 8 | HG01496.hp2 HG02155.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488-1532_1488-151 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(9): Show |
1 | a0001c0001t0001g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1488-1534_1488-151 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(11): Show |
3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1488-1536_1488-151 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
G | GACACACA others(13): Show |
1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1488-1538_1488-151 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
GAC | G | 4 | a0001c0001t0001g0130a0001c0001t0023g0131a0001c0001t0043g0134others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-1520_1488-151 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186136
|
GACACAC | G | 5 | a0001c0001t0004g0257a0001c0001t0004g0266a0002c0003t0003g0089others(2): Show | 5 | HG01069.hp1 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488-1524_1488-151 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186136 | |||||
| chr3:154186273
|
G | A | 61 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1488-1412G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186273 | ||||||
| chr3:154186370
|
TATA | T | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488-1312_1488-131 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186370 | |||||
| chr3:154186518
|
C | T | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488-1167C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186518 | ||||||
| chr3:154186559
|
G | A | 61 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1488-1126G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186559 | ||||||
| chr3:154186886
|
C | CT | 78 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.1488-771dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTT | 34 | a0001c0001t0001g0177a0001c0001t0001g0185a0001c0001t0001g0189others(31): Show | 34 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1488-772_1488-771d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTT | 23 | a0001c0001t0001g0130a0001c0001t0001g0187a0001c0001t0001g0188others(20): Show | 23 | HG00741.hp2 HG01123.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1488-773_1488-771d others(5): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTTT | 27 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0191others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1488-774_1488-771d others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTTTT | 8 | a0001c0001t0002g0217a0001c0001t0002g0226a0001c0001t0002g0237others(5): Show | 8 | HG00735.hp2 HG01109.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488-775_1488-771d others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTTTTTT others(4): Show |
2 | a0002c0003t0018g0092a0002c0003t0046g0093 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1488-781_1488-771d others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTTTTTT others(5): Show |
1 | a0002c0003t0044g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1488-782_1488-771d others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
C | CTTTTTTT others(9): Show |
1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1488-786_1488-771d others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1488-781_1488-771d others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
CTTTTTTT others(8): Show |
C | 70 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(67): Show | 70 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.1488-785_1488-771d others(17): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154186886
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0017g0132a0002c0002t0003g0053a0007c0006t0017g0128others(1): Show | 4 | HG01884.hp2 HG01993.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-786_1488-771d others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154186886 | |||||
| chr3:154187245
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1488-440A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154187245 | ||||||
| chr3:154187310
|
T | C | 1 | a0001c0001t0007g0220 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1488-375T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154187310 | ||||||
| chr3:154187346
|
A | G | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1488-339A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154187346 | ||||||
| chr3:154187380
|
A | AT | 142 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(139): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1488-286dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154187380 | |||||
| chr3:154187380
|
AT | A | 8 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(5): Show | 8 | HG01517.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488-286delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr3 | 154187380 | |||||
| chr3:154187475
|
C | T | 12 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1488-210C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154187475 | ||||||
| chr3:154187572
|
C | T | 2 | a0001c0001t0004g0005a0001c0001t0004g0262 | 3 | NA19004.hp2 NA19082.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1488-113C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154187572 | ||||||
| chr3:154187925
|
A | G | 1 | a0001c0001t0041g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1640+88A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154187925 | ||||||
| chr3:154187977
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1640+140A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154187977 | ||||||
| chr3:154187995
|
A | T | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1640+158A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154187995 | ||||||
| chr3:154188199
|
T | A | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1640+362T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154188199 | ||||||
| chr3:154188259
|
A | G | 4 | a0001c0001t0007g0274a0001c0001t0014g0276a0001c0001t0014g0277others(1): Show | 4 | HG02258.hp1 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640+422A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154188259 | ||||||
| chr3:154188320
|
A | G | 2 | a0002c0002t0024g0035a0002c0002t0024g0062 | 2 | HG02071.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1640+483A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154188320 | ||||||
| chr3:154188756
|
A | C | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1640+919A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154188756 | ||||||
| chr3:154188816
|
CTTCATGA others(4): Show |
C | 76 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(73): Show | 76 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.1640+985_1640+995d others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154188816 | |||||
| chr3:154188853
|
A | G | 50 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(47): Show | 51 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1640+1016A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154188853 | ||||||
| chr3:154189059
|
C | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1640+1222C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189059 | ||||||
| chr3:154189069
|
C | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1640+1232C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189069 | ||||||
| chr3:154189086
|
C | T | 1 | a0002c0003t0048g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1640+1249C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189086 | ||||||
| chr3:154189200
|
A | T | 129 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1640+1363A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189200 | ||||||
| chr3:154189229
|
A | G | 1 | a0001c0001t0012g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1640+1392A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189229 | ||||||
| chr3:154189334
|
A | AT | 133 | a0001c0001t0001g0254a0001c0001t0001g0268a0001c0001t0001g0269others(130): Show | 134 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1640+1518dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154189334 | |||||
| chr3:154189334
|
A | ATT | 6 | a0001c0001t0001g0204a0001c0001t0002g0217a0001c0001t0002g0237others(3): Show | 6 | HG01109.hp1 HG02074.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1640+1517_1640+151 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154189334 | |||||
| chr3:154189334
|
AT | A | 28 | a0001c0001t0001g0146a0001c0001t0002g0213a0001c0001t0004g0005others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1640+1518delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154189334 | |||||
| chr3:154189539
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1640+1702G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189539 | ||||||
| chr3:154189551
|
A | G | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1640+1714A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189551 | ||||||
| chr3:154189827
|
G | GT | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1641-1457dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154189827 | |||||
| chr3:154189833
|
G | GT | 75 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(72): Show | 75 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.1641-1444dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr3 | 154189833 | |||||
| chr3:154189833
|
G | T | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1641-1456G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189833 | ||||||
| chr3:154189869
|
G | A | 62 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0156others(59): Show | 63 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1641-1420G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189869 | ||||||
| chr3:154189872
|
A | G | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1641-1417A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189872 | ||||||
| chr3:154189932
|
A | G | 5 | a0002c0002t0005g0034a0002c0002t0005g0042a0002c0002t0005g0043others(2): Show | 5 | HG01243.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1641-1357A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154189932 | ||||||
| chr3:154190001
|
T | A | 103 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.1641-1288T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190001 | ||||||
| chr3:154190028
|
T | A | 1 | a0001c0001t0002g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1641-1261T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190028 | ||||||
| chr3:154190029
|
T | A | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 49 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1641-1260T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190029 | ||||||
| chr3:154190030
|
T | A | 49 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(46): Show | 49 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1641-1259T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190030 | ||||||
| chr3:154190135
|
A | G | 3 | a0001c0001t0004g0171a0001c0001t0004g0219a0001c0001t0004g0250 | 3 | HG00099.hp2 HG00323.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1641-1154A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190135 | ||||||
| chr3:154190154
|
G | A | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1641-1135G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190154 | ||||||
| chr3:154190268
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1641-1021T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190268 | ||||||
| chr3:154190294
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1641-995T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190294 | ||||||
| chr3:154190370
|
G | A | 2 | a0002c0002t0028g0077a0002c0002t0028g0078 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1641-919G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190370 | ||||||
| chr3:154190558
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1641-731G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190558 | ||||||
| chr3:154190638
|
T | G | 13 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0187others(10): Show | 13 | HG00597.hp2 HG00738.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1641-651T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190638 | ||||||
| chr3:154190649
|
G | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1641-640G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190649 | ||||||
| chr3:154190922
|
A | G | 1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1641-367A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190922 | ||||||
| chr3:154191798
|
A | G | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | NA18951.hp2 NA18986.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+380A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154191798 | ||||||
| chr3:154192030
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1770+612A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154192030 | ||||||
| chr3:154192157
|
T | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1770+739T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154192157 | ||||||
| chr3:154192199
|
T | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1770+781T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154192199 | ||||||
| chr3:154192265
|
T | A | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1770+847T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154192265 | ||||||
| chr3:154193053
|
A | AC | 76 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(73): Show | 76 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.1771-1584dupC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 154193053 | |||||
| chr3:154193101
|
A | G | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1771-1543A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193101 | ||||||
| chr3:154193176
|
T | C | 1 | a0001c0001t0012g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1771-1468T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193176 | ||||||
| chr3:154193206
|
C | T | 107 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1771-1438C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193206 | ||||||
| chr3:154193447
|
G | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1771-1197G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193447 | ||||||
| chr3:154193503
|
A | G | 1 | a0002c0003t0006g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1771-1141A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193503 | ||||||
| chr3:154193546
|
CAT | C | 44 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0169others(41): Show | 44 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1771-1097_1771-109 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193546 | ||||||
| chr3:154193660
|
C | T | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1771-984C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193660 | ||||||
| chr3:154193669
|
A | G | 1 | a0001c0001t0004g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1771-975A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193669 | ||||||
| chr3:154193670
|
A | T | 1 | a0001c0001t0004g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1771-974A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193670 | ||||||
| chr3:154193700
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1771-944A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193700 | ||||||
| chr3:154193798
|
A | G | 2 | a0001c0001t0002g0191a0001c0001t0002g0230 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1771-846A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193798 | ||||||
| chr3:154193842
|
G | GT | 50 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(47): Show | 51 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1771-793dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 154193842 | |||||
| chr3:154193842
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1771-793_1771-792i others(13): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 154193842 | |||||
| chr3:154193842
|
G | GTTTTTTT others(5): Show |
1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1771-793_1771-792i others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | 154193842 | |||||
| chr3:154193843
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1771-801T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193843 | ||||||
| chr3:154193915
|
A | G | 1 | a0002c0002t0003g0024 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1771-729A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193915 | ||||||
| chr3:154193936
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1771-708G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154193936 | ||||||
| chr3:154194310
|
C | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1771-334C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154194310 | ||||||
| chr3:154194448
|
C | A | 4 | a0002c0002t0005g0034a0002c0002t0005g0042a0002c0002t0005g0043others(1): Show | 4 | HG01243.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1771-196C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154194448 | ||||||
| chr3:154194481
|
T | C | 23 | a0002c0002t0003g0025a0002c0002t0005g0060a0002c0003t0004g0085others(20): Show | 24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1771-163T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154194481 | ||||||
| chr3:154194835
|
C | T | 1 | a0001c0001t0012g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1845+117C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154194835 | ||||||
| chr3:154194852
|
C | A | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1845+134C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154194852 | ||||||
| chr3:154194867
|
T | C | 1 | a0009c0016t0001g0218 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1845+149T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154194867 | ||||||
| chr3:154194925
|
G | A | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1845+207G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154194925 | ||||||
| chr3:154195293
|
C | G | 2 | a0002c0002t0003g0023a0002c0002t0003g0050 | 2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1845+575C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195293 | ||||||
| chr3:154195350
|
T | C | 1 | a0002c0002t0006g0030 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1845+632T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195350 | ||||||
| chr3:154195359
|
A | T | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1845+641A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195359 | ||||||
| chr3:154195383
|
C | T | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1845+665C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195383 | ||||||
| chr3:154195489
|
C | T | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+771C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195489 | ||||||
| chr3:154195614
|
G | A | 262 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1845+896G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195614 | ||||||
| chr3:154195712
|
A | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+994A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195712 | ||||||
| chr3:154195771
|
T | C | 1 | a0002c0002t0003g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1845+1053T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195771 | ||||||
| chr3:154195777
|
A | G | 1 | a0002c0002t0003g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1845+1059A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195777 | ||||||
| chr3:154195977
|
C | T | 1 | a0001c0001t0012g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1845+1259C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154195977 | ||||||
| chr3:154196174
|
G | A | 207 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1845+1456G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196174 | ||||||
| chr3:154196191
|
G | A | 6 | a0001c0001t0035g0255a0002c0002t0051g0033a0002c0003t0018g0092others(3): Show | 6 | HG02886.hp2 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1845+1473G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196191 | ||||||
| chr3:154196255
|
G | A | 1 | a0001c0001t0015g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1845+1537G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196255 | ||||||
| chr3:154196333
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+1615A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196333 | ||||||
| chr3:154196553
|
A | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+1835A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196553 | ||||||
| chr3:154196602
|
G | A | 1 | a0002c0002t0003g0025 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1845+1884G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196602 | ||||||
| chr3:154196638
|
C | G | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1845+1920C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196638 | ||||||
| chr3:154196690
|
C | T | 1 | a0002c0002t0049g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1845+1972C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154196690 | ||||||
| chr3:154196886
|
G | GA | 25 | a0002c0002t0003g0025a0002c0002t0005g0060a0002c0003t0004g0085others(22): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1845+2179dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154196886 | |||||
| chr3:154197102
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0011g0002 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1845+2384A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197102 | ||||||
| chr3:154197113
|
A | G | 105 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0153others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1845+2395A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197113 | ||||||
| chr3:154197243
|
G | A | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+2525G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197243 | ||||||
| chr3:154197270
|
T | A | 5 | a0002c0002t0051g0033a0002c0003t0018g0092a0002c0003t0044g0094others(2): Show | 5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1845+2552T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197270 | ||||||
| chr3:154197290
|
C | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+2572C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197290 | ||||||
| chr3:154197465
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+2747G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197465 | ||||||
| chr3:154197628
|
T | C | 267 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1845+2910T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197628 | ||||||
| chr3:154197679
|
T | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+2961T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197679 | ||||||
| chr3:154197979
|
A | C | 2 | a0001c0001t0036g0205a0006c0013t0025g0019 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1845+3261A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154197979 | ||||||
| chr3:154198139
|
G | T | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+3421G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198139 | ||||||
| chr3:154198145
|
C | T | 2 | a0002c0002t0003g0061a0011c0018t0007g0006 | 2 | HG01496.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1845+3427C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198145 | ||||||
| chr3:154198216
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0002g0190a0001c0001t0011g0002 | 3 | HG00280.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1845+3498A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198216 | ||||||
| chr3:154198227
|
G | A | 1 | a0002c0002t0049g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1845+3509G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198227 | ||||||
| chr3:154198416
|
A | C | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1845+3698A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198416 | ||||||
| chr3:154198659
|
T | A | 2 | a0002c0002t0049g0055a0002c0014t0019g0040 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1845+3941T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198659 | ||||||
| chr3:154198713
|
A | T | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+3995A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198713 | ||||||
| chr3:154198878
|
A | C | 3 | a0003c0004t0002g0007a0003c0004t0004g0011a0003c0004t0010g0009 | 3 | HG01081.hp2 HG01106.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1845+4160A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198878 | ||||||
| chr3:154198994
|
G | T | 1 | a0002c0003t0006g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1845+4276G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154198994 | ||||||
| chr3:154199452
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1845+4734A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199452 | ||||||
| chr3:154199563
|
T | G | 1 | a0001c0001t0002g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1845+4845T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199563 | ||||||
| chr3:154199606
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1845+4888G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199606 | ||||||
| chr3:154199650
|
A | G | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1845+4932A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199650 | ||||||
| chr3:154199730
|
T | C | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+5012T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199730 | ||||||
| chr3:154199804
|
G | A | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1845+5086G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199804 | ||||||
| chr3:154199867
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1845+5149A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199867 | ||||||
| chr3:154199873
|
A | G | 2 | a0001c0001t0014g0277a0001c0001t0039g0275 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1845+5155A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154199873 | ||||||
| chr3:154200330
|
T | C | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+5612T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154200330 | ||||||
| chr3:154200336
|
T | C | 1 | a0002c0014t0019g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1845+5618T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154200336 | ||||||
| chr3:154200562
|
T | C | 30 | a0001c0001t0001g0146a0001c0001t0002g0213a0001c0001t0004g0005others(27): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(29): Show |
intron_variant | MODIFIER | c.1845+5844T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154200562 | ||||||
| chr3:154200886
|
A | T | 1 | a0002c0003t0026g0110 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1845+6168A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154200886 | ||||||
| chr3:154200925
|
G | A | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+6207G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154200925 | ||||||
| chr3:154201004
|
A | AT | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+6295dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154201004 | |||||
| chr3:154201160
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1845+6442G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201160 | ||||||
| chr3:154201207
|
T | G | 1 | a0002c0003t0005g0001 | 2 | NA18962.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1845+6489T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201207 | ||||||
| chr3:154201309
|
C | T | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1845+6591C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201309 | ||||||
| chr3:154201338
|
A | C | 2 | a0002c0002t0005g0042a0002c0002t0005g0043 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1845+6620A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201338 | ||||||
| chr3:154201429
|
G | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+6711G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201429 | ||||||
| chr3:154201466
|
A | G | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+6748A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201466 | ||||||
| chr3:154201510
|
T | A | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+6792T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201510 | ||||||
| chr3:154201689
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+6971T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201689 | ||||||
| chr3:154201749
|
A | G | 3 | a0002c0002t0006g0027a0002c0002t0006g0029a0002c0002t0006g0063 | 3 | NA18946.hp2 NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1845+7031A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201749 | ||||||
| chr3:154201775
|
T | C | 1 | a0001c0001t0034g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1845+7057T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201775 | ||||||
| chr3:154201839
|
G | T | 11 | a0001c0001t0017g0132a0001c0001t0037g0256a0002c0002t0005g0034others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1845+7121G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201839 | ||||||
| chr3:154201946
|
T | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+7228T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201946 | ||||||
| chr3:154201979
|
C | A | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1845+7261C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154201979 | ||||||
| chr3:154202024
|
C | T | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+7306C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202024 | ||||||
| chr3:154202100
|
A | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0235 | 2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1845+7382A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202100 | ||||||
| chr3:154202110
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+7392T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202110 | ||||||
| chr3:154202299
|
G | A | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+7581G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202299 | ||||||
| chr3:154202310
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1845+7592G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202310 | ||||||
| chr3:154202322
|
C | T | 1 | a0002c0003t0005g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1845+7604C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202322 | ||||||
| chr3:154202337
|
G | A | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1845+7619G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202337 | ||||||
| chr3:154202614
|
T | C | 3 | a0001c0001t0002g0152a0001c0001t0004g0278a0001c0001t0029g0151 | 3 | HG03239.hp2 HG03710.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1845+7896T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202614 | ||||||
| chr3:154202624
|
C | G | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+7906C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202624 | ||||||
| chr3:154202775
|
G | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+8057G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202775 | ||||||
| chr3:154202786
|
T | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+8068T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202786 | ||||||
| chr3:154202798
|
C | CTGTT | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+8083_1845+808 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154202798 | |||||
| chr3:154202884
|
T | G | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0039g0275 | 3 | HG02886.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1845+8166T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202884 | ||||||
| chr3:154202911
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+8193A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202911 | ||||||
| chr3:154202947
|
G | T | 1 | a0001c0001t0007g0206 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1845+8229G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202947 | ||||||
| chr3:154202953
|
A | G | 4 | a0002c0003t0005g0135a0002c0003t0006g0096a0002c0003t0026g0103others(1): Show | 4 | HG01433.hp1 HG01884.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+8235A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202953 | ||||||
| chr3:154202965
|
G | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+8247G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154202965 | ||||||
| chr3:154203005
|
G | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1845+8287G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203005 | ||||||
| chr3:154203077
|
A | C | 23 | a0002c0002t0003g0025a0002c0002t0005g0060a0002c0003t0004g0085others(20): Show | 24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1845+8359A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203077 | ||||||
| chr3:154203209
|
G | A | 1 | a0002c0003t0005g0108 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1845+8491G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203209 | ||||||
| chr3:154203264
|
T | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+8546T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203264 | ||||||
| chr3:154203296
|
A | G | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+8578A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203296 | ||||||
| chr3:154203369
|
G | A | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1845+8651G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203369 | ||||||
| chr3:154203388
|
G | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+8670G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203388 | ||||||
| chr3:154203395
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1845+8677G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203395 | ||||||
| chr3:154203398
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1845+8680A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203398 | ||||||
| chr3:154203567
|
T | C | 1 | a0001c0001t0004g0257 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1845+8849T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203567 | ||||||
| chr3:154203686
|
C | T | 30 | a0001c0001t0007g0172a0001c0001t0007g0175a0002c0002t0003g0024others(27): Show | 30 | HG00597.hp1 HG01081.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1845+8968C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203686 | ||||||
| chr3:154203830
|
G | A | 1 | a0002c0002t0024g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1845+9112G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203830 | ||||||
| chr3:154203846
|
C | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+9128C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203846 | ||||||
| chr3:154203850
|
CT | C | 7 | a0001c0001t0002g0191a0001c0001t0002g0271a0001c0001t0021g0133others(4): Show | 7 | HG01168.hp2 HG01433.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1845+9145delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154203850 | |||||
| chr3:154203922
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+9204G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203922 | ||||||
| chr3:154203944
|
T | C | 48 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1845+9226T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203944 | ||||||
| chr3:154203977
|
G | T | 2 | a0002c0002t0049g0055a0002c0014t0019g0040 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1845+9259G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154203977 | ||||||
| chr3:154204164
|
A | G | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1845+9446A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204164 | ||||||
| chr3:154204216
|
A | G | 1 | a0001c0001t0015g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1845+9498A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204216 | ||||||
| chr3:154204277
|
GT | G | 49 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0167others(46): Show | 49 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1845+9563delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154204277 | |||||
| chr3:154204299
|
G | T | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+9581G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204299 | ||||||
| chr3:154204316
|
A | G | 1 | a0001c0001t0011g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1845+9598A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204316 | ||||||
| chr3:154204333
|
C | CT | 208 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(205): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1845+9633dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154204333 | |||||
| chr3:154204333
|
C | CTT | 51 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(48): Show | 51 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1845+9632_1845+963 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154204333 | |||||
| chr3:154204365
|
T | C | 263 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1845+9647T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204365 | ||||||
| chr3:154204438
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+9720G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204438 | ||||||
| chr3:154204507
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+9789T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204507 | ||||||
| chr3:154204537
|
G | T | 2 | a0002c0002t0003g0052a0002c0002t0008g0020 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1845+9819G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204537 | ||||||
| chr3:154204617
|
A | C | 1 | a0001c0001t0015g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1845+9899A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204617 | ||||||
| chr3:154204621
|
T | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+9903T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204621 | ||||||
| chr3:154204640
|
T | C | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1845+9922T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204640 | ||||||
| chr3:154204739
|
C | T | 47 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(44): Show | 47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1845+10021C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204739 | ||||||
| chr3:154204751
|
A | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+10033A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204751 | ||||||
| chr3:154204752
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1845+10034C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204752 | ||||||
| chr3:154204980
|
G | A | 1 | a0002c0002t0024g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1845+10262G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154204980 | ||||||
| chr3:154205024
|
G | A | 209 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(206): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1845+10306G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205024 | ||||||
| chr3:154205309
|
A | G | 1 | a0002c0002t0003g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1845+10591A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205309 | ||||||
| chr3:154205391
|
T | C | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1845+10673T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205391 | ||||||
| chr3:154205413
|
G | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+10695G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205413 | ||||||
| chr3:154205484
|
A | G | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+10766A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205484 | ||||||
| chr3:154205574
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1845+10856G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205574 | ||||||
| chr3:154205580
|
C | T | 1 | a0002c0002t0003g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1845+10862C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205580 | ||||||
| chr3:154205629
|
A | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1845+10911A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205629 | ||||||
| chr3:154205729
|
G | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1845+11011G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154205729 | ||||||
| chr3:154205740
|
GA | G | 4 | a0002c0003t0005g0135a0002c0003t0006g0096a0002c0003t0026g0103others(1): Show | 4 | HG01433.hp1 HG01884.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1845+11025delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154205740 | |||||
| chr3:154206076
|
T | A | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0039g0275 | 3 | HG02886.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1845+11358T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206076 | ||||||
| chr3:154206277
|
A | G | 11 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(8): Show | 11 | HG01243.hp1 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1845+11559A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206277 | ||||||
| chr3:154206675
|
C | T | 1 | a0002c0002t0003g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1846-11194C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206675 | ||||||
| chr3:154206785
|
C | T | 43 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(40): Show | 43 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1846-11084C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206785 | ||||||
| chr3:154206805
|
G | A | 1 | a0002c0002t0003g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1846-11064G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206805 | ||||||
| chr3:154206874
|
TACAGTAT others(5): Show |
T | 1 | a0002c0003t0048g0097 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1846-10990_1846-10 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154206874 | |||||
| chr3:154206896
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1846-10973T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206896 | ||||||
| chr3:154206995
|
A | G | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-10874A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154206995 | ||||||
| chr3:154207024
|
TTAAA | T | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1846-10839_1846-10 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154207024 | |||||
| chr3:154207175
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1846-10694C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154207175 | ||||||
| chr3:154207208
|
G | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-10661G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154207208 | ||||||
| chr3:154207218
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1846-10651C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154207218 | ||||||
| chr3:154207689
|
G | A | 4 | a0002c0003t0018g0092a0002c0003t0044g0094a0002c0003t0045g0095others(1): Show | 4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-10180G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154207689 | ||||||
| chr3:154208064
|
G | T | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1846-9805G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208064 | ||||||
| chr3:154208334
|
C | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-9535C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208334 | ||||||
| chr3:154208536
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-9333G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208536 | ||||||
| chr3:154208556
|
T | C | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1846-9313T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208556 | ||||||
| chr3:154208635
|
C | A | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1846-9234C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208635 | ||||||
| chr3:154208763
|
A | AT | 89 | a0001c0001t0001g0234a0001c0001t0002g0229a0001c0001t0007g0144others(86): Show | 90 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1846-9086dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154208763 | |||||
| chr3:154208763
|
A | ATT | 7 | a0002c0002t0003g0084a0002c0002t0005g0028a0002c0002t0006g0029others(4): Show | 7 | HG00408.hp1 HG03098.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1846-9087_1846-908 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154208763 | |||||
| chr3:154208763
|
AT | A | 24 | a0001c0001t0001g0130a0001c0001t0001g0157a0001c0001t0001g0268others(21): Show | 25 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1846-9086delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154208763 | |||||
| chr3:154208816
|
A | T | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1846-9053A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208816 | ||||||
| chr3:154208955
|
C | T | 132 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1846-8914C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208955 | ||||||
| chr3:154208978
|
A | G | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-8891A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154208978 | ||||||
| chr3:154209172
|
A | G | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-8697A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209172 | ||||||
| chr3:154209353
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1846-8516A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209353 | ||||||
| chr3:154209423
|
T | C | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1846-8446T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209423 | ||||||
| chr3:154209640
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-8229A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209640 | ||||||
| chr3:154209750
|
C | G | 23 | a0001c0001t0001g0181a0001c0001t0001g0188a0001c0001t0001g0198others(20): Show | 24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1846-8119C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209750 | ||||||
| chr3:154209792
|
T | A | 2 | a0002c0002t0005g0042a0002c0002t0005g0043 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1846-8077T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209792 | ||||||
| chr3:154209962
|
A | C | 1 | a0007c0006t0017g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1846-7907A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154209962 | ||||||
| chr3:154210003
|
G | A | 193 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1846-7866G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210003 | ||||||
| chr3:154210042
|
A | G | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1846-7827A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210042 | ||||||
| chr3:154210105
|
G | C | 1 | a0002c0003t0005g0113 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1846-7764G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210105 | ||||||
| chr3:154210166
|
G | A | 5 | a0001c0001t0007g0206a0002c0003t0003g0098a0006c0012t0008g0018others(2): Show | 5 | HG01255.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1846-7703G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210166 | ||||||
| chr3:154210516
|
T | C | 14 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0169others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1846-7353T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210516 | ||||||
| chr3:154210595
|
G | A | 2 | a0001c0001t0009g0004a0001c0001t0009g0261 | 3 | HG02280.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1846-7274G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210595 | ||||||
| chr3:154210607
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-7262A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210607 | ||||||
| chr3:154210707
|
C | T | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1846-7162C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210707 | ||||||
| chr3:154210762
|
C | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-7107C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210762 | ||||||
| chr3:154210766
|
A | G | 1 | a0001c0001t0004g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1846-7103A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210766 | ||||||
| chr3:154210777
|
A | G | 1 | a0001c0001t0041g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1846-7092A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210777 | ||||||
| chr3:154210802
|
T | G | 279 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(276): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1846-7067T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210802 | ||||||
| chr3:154210921
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1846-6948C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210921 | ||||||
| chr3:154210963
|
G | T | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-6906G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210963 | ||||||
| chr3:154211003
|
G | A | 19 | a0001c0001t0001g0201a0002c0002t0005g0060a0002c0003t0005g0001others(16): Show | 20 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.1846-6866G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154211003 | ||||||
| chr3:154211078
|
G | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-6791G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154211078 | ||||||
| chr3:154211634
|
T | C | 17 | a0001c0001t0007g0206a0001c0001t0017g0132a0001c0001t0037g0256others(14): Show | 17 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1846-6235T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154211634 | ||||||
| chr3:154211867
|
A | ATG | 110 | a0001c0001t0001g0201a0001c0001t0001g0254a0001c0001t0007g0144others(107): Show | 111 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1846-5984_1846-598 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154211867 | |||||
| chr3:154211867
|
A | ATGTG | 102 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1846-5986_1846-598 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154211867 | |||||
| chr3:154211867
|
A | ATGTGTG | 48 | a0001c0001t0001g0204a0001c0001t0002g0152a0001c0001t0002g0161others(45): Show | 50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1846-5988_1846-598 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154211867 | |||||
| chr3:154211867
|
ATG | A | 7 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1846-5984_1846-598 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154211867 | |||||
| chr3:154211896
|
A | T | 1 | a0001c0001t0034g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1846-5973A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154211896 | ||||||
| chr3:154212006
|
T | C | 265 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1846-5863T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212006 | ||||||
| chr3:154212015
|
G | A | 1 | a0001c0001t0007g0172 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1846-5854G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212015 | ||||||
| chr3:154212036
|
T | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG02257.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1846-5833T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212036 | ||||||
| chr3:154212113
|
C | T | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1846-5756C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212113 | ||||||
| chr3:154212137
|
G | A | 1 | a0004c0005t0013g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1846-5732G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212137 | ||||||
| chr3:154212201
|
T | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-5668T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212201 | ||||||
| chr3:154212217
|
A | C | 59 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(56): Show | 59 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.1846-5652A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212217 | ||||||
| chr3:154212331
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1846-5538G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212331 | ||||||
| chr3:154212341
|
CA | C | 256 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1846-5514delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154212341 | |||||
| chr3:154212491
|
T | C | 4 | a0001c0001t0002g0225a0001c0001t0002g0229a0001c0001t0009g0227others(1): Show | 4 | HG00738.hp2 HG01167.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-5378T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212491 | ||||||
| chr3:154212520
|
G | T | 2 | a0001c0001t0001g0195a0001c0001t0004g0193 | 2 | NA18953.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1846-5349G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212520 | ||||||
| chr3:154212592
|
C | T | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-5277C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212592 | ||||||
| chr3:154212753
|
G | A | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-5116G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212753 | ||||||
| chr3:154212830
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-5039G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212830 | ||||||
| chr3:154212949
|
G | A | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1846-4920G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154212949 | ||||||
| chr3:154213019
|
T | G | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1846-4850T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213019 | ||||||
| chr3:154213061
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-4808T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213061 | ||||||
| chr3:154213172
|
T | A | 212 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(209): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1846-4697T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213172 | ||||||
| chr3:154213201
|
T | G | 3 | a0001c0001t0021g0133a0002c0003t0025g0105a0005c0008t0014g0122 | 3 | HG02717.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1846-4668T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213201 | ||||||
| chr3:154213201
|
T | TAG | 185 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1846-4653_1846-465 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213201 | |||||
| chr3:154213201
|
T | TAGAG | 8 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | HG01433.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1846-4655_1846-465 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213201 | |||||
| chr3:154213214
|
A | AGT | 4 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-4654_1846-465 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213214 | |||||
| chr3:154213216
|
A | AGAGAGTG others(7): Show |
1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1846-4652_1846-465 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213216 | |||||
| chr3:154213216
|
A | AGAGT | 15 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0023g0131others(12): Show | 15 | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1846-4652_1846-465 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213216 | |||||
| chr3:154213216
|
A | T | 6 | a0001c0001t0002g0224a0001c0001t0015g0124a0001c0001t0015g0126others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1846-4653A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213216 | ||||||
| chr3:154213218
|
T | A | 101 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0167others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1846-4651T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213218 | ||||||
| chr3:154213220
|
T | A | 5 | a0001c0001t0002g0152a0001c0001t0002g0249a0001c0001t0029g0151others(2): Show | 5 | HG02109.hp1 HG02135.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1846-4649T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213220 | ||||||
| chr3:154213225
|
G | A | 1 | a0002c0003t0003g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1846-4644G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213225 | ||||||
| chr3:154213239
|
G | GTATA | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-4629_1846-462 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213239 | |||||
| chr3:154213241
|
G | A | 5 | a0001c0001t0002g0224a0001c0001t0002g0238a0002c0003t0018g0092others(2): Show | 5 | HG00735.hp2 HG03669.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1846-4628G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213241 | ||||||
| chr3:154213241
|
G | GTGTATAT others(3): Show |
34 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(31): Show | 34 | HG00609.hp2 HG00738.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1846-4627_1846-462 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213241 | |||||
| chr3:154213241
|
G | GTGTATAT others(5): Show |
2 | a0001c0001t0002g0265a0001c0001t0020g0003 | 3 | HG00140.hp1 HG00280.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1846-4627_1846-462 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213241 | |||||
| chr3:154213241
|
G | GTGTGTAT others(3): Show |
3 | a0001c0001t0002g0217a0001c0001t0002g0233a0001c0001t0002g0235 | 3 | HG01361.hp1 HG02074.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1846-4627_1846-462 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213241 | |||||
| chr3:154213241
|
G | GTGTGTAT others(5): Show |
1 | a0001c0015t0002g0143 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1846-4627_1846-462 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154213241 | |||||
| chr3:154213243
|
A | G | 206 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1846-4626A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213243 | ||||||
| chr3:154213245
|
A | G | 11 | a0001c0001t0021g0133a0001c0001t0035g0255a0001c0001t0041g0165others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1846-4624A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213245 | ||||||
| chr3:154213255
|
A | G | 1 | a0001c0001t0021g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1846-4614A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213255 | ||||||
| chr3:154213256
|
T | C | 1 | a0001c0001t0021g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1846-4613T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213256 | ||||||
| chr3:154213353
|
A | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-4516A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213353 | ||||||
| chr3:154213455
|
G | GA | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-4414_1846-441 others(5): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213455 | ||||||
| chr3:154213553
|
G | C | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1846-4316G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213553 | ||||||
| chr3:154213817
|
T | A | 1 | a0001c0001t0004g0147 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1846-4052T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213817 | ||||||
| chr3:154213889
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0016g0264 | 3 | NA18951.hp2 NA18986.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1846-3980C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213889 | ||||||
| chr3:154213921
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1846-3948A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213921 | ||||||
| chr3:154214071
|
A | G | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-3798A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154214071 | ||||||
| chr3:154214529
|
G | C | 2 | a0002c0002t0003g0039a0002c0002t0003g0057 | 2 | HG02165.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1846-3340G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154214529 | ||||||
| chr3:154214614
|
A | C | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-3255A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154214614 | ||||||
| chr3:154214660
|
T | C | 13 | a0002c0002t0003g0026a0002c0002t0003g0065a0002c0002t0003g0068others(10): Show | 13 | HG00558.hp2 HG02015.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1846-3209T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154214660 | ||||||
| chr3:154215012
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-2857G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215012 | ||||||
| chr3:154215099
|
A | T | 1 | a0001c0001t0004g0168 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1846-2770A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215099 | ||||||
| chr3:154215330
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-2539T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215330 | ||||||
| chr3:154215397
|
A | AT | 38 | a0001c0001t0001g0146a0001c0001t0002g0213a0001c0001t0004g0005others(35): Show | 40 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1846-2459dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154215397 | |||||
| chr3:154215409
|
T | C | 1 | a0002c0002t0003g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1846-2460T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215409 | ||||||
| chr3:154215430
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1846-2439G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215430 | ||||||
| chr3:154215466
|
C | T | 1 | a0002c0003t0005g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1846-2403C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215466 | ||||||
| chr3:154215611
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1846-2258T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154215611 | ||||||
| chr3:154216040
|
A | G | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1846-1829A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216040 | ||||||
| chr3:154216102
|
T | C | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1846-1767T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216102 | ||||||
| chr3:154216171
|
A | G | 1 | a0001c0001t0016g0264 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1846-1698A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216171 | ||||||
| chr3:154216232
|
G | A | 2 | a0001c0001t0007g0274a0002c0002t0005g0028 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1846-1637G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216232 | ||||||
| chr3:154216482
|
T | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1846-1387T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216482 | ||||||
| chr3:154216486
|
T | A | 2 | a0001c0001t0001g0181a0002c0003t0025g0105 | 2 | NA18522.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1846-1383T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216486 | ||||||
| chr3:154216489
|
T | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1846-1380T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216489 | ||||||
| chr3:154216491
|
T | A | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1846-1378T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216491 | ||||||
| chr3:154216491
|
TA | T | 4 | a0001c0001t0001g0167a0001c0001t0004g0210a0001c0015t0002g0143others(1): Show | 4 | HG01257.hp2 HG02258.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-1377delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216491 | ||||||
| chr3:154216492
|
A | T | 259 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(256): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1846-1377A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216492 | ||||||
| chr3:154216494
|
T | A | 252 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1846-1375T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216494 | ||||||
| chr3:154216502
|
A | T | 2 | a0001c0001t0035g0255a0005c0008t0014g0122 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-1367A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216502 | ||||||
| chr3:154216503
|
TTTTTTA | T | 56 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0182others(53): Show | 56 | HG00558.hp2 HG01081.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.1846-1360_1846-135 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154216503 | |||||
| chr3:154216505
|
T | A | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1846-1364T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216505 | ||||||
| chr3:154216506
|
T | A | 9 | a0001c0001t0001g0268a0001c0001t0002g0236a0001c0001t0009g0004others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1846-1363T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216506 | ||||||
| chr3:154216506
|
TTTA | T | 10 | a0001c0001t0001g0223a0001c0001t0004g0215a0001c0001t0007g0175others(7): Show | 10 | HG01069.hp1 HG02109.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1846-1360_1846-135 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154216506 | |||||
| chr3:154216507
|
T | A | 4 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0273others(1): Show | 4 | NA18946.hp1 NA18948.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-1362T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216507 | ||||||
| chr3:154216507
|
TTA | T | 123 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(120): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1846-1360_1846-135 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr3 | 154216507 | |||||
| chr3:154216508
|
TA | T | 69 | a0001c0001t0001g0204a0001c0001t0001g0254a0001c0001t0001g0268others(66): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1846-1360delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216508 | ||||||
| chr3:154216509
|
A | T | 6 | a0001c0001t0021g0133a0001c0001t0035g0255a0002c0003t0018g0092others(3): Show | 6 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1846-1360A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216509 | ||||||
| chr3:154216510
|
T | A | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1846-1359T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216510 | ||||||
| chr3:154216511
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1846-1358T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216511 | ||||||
| chr3:154216512
|
T | A | 6 | a0001c0001t0004g0149a0001c0001t0014g0276a0001c0001t0014g0277others(3): Show | 6 | HG00621.hp2 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1846-1357T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216512 | ||||||
| chr3:154216513
|
T | A | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1846-1356T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216513 | ||||||
| chr3:154216514
|
T | A | 1 | a0002c0002t0028g0078 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1846-1355T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216514 | ||||||
| chr3:154216519
|
T | A | 4 | a0001c0001t0001g0254a0001c0001t0041g0165a0001c0009t0022g0163others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-1350T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216519 | ||||||
| chr3:154216620
|
G | T | 1 | a0002c0002t0028g0078 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1846-1249G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216620 | ||||||
| chr3:154216685
|
T | C | 2 | a0001c0001t0002g0247a0002c0003t0005g0112 | 2 | HG03927.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1846-1184T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216685 | ||||||
| chr3:154216686
|
T | C | 266 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1846-1183T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216686 | ||||||
| chr3:154216778
|
C | T | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1846-1091C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216778 | ||||||
| chr3:154216997
|
G | A | 1 | a0001c0001t0002g0259 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1846-872G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216997 | ||||||
| chr3:154217001
|
A | G | 276 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(273): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1846-868A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217001 | ||||||
| chr3:154217080
|
T | C | 1 | a0002c0003t0006g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1846-789T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217080 | ||||||
| chr3:154217105
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-764A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217105 | ||||||
| chr3:154217144
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1846-725C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217144 | ||||||
| chr3:154217220
|
T | C | 3 | a0001c0001t0021g0133a0002c0003t0045g0095a0005c0008t0014g0122 | 3 | HG02717.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1846-649T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217220 | ||||||
| chr3:154217221
|
G | A | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1846-648G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217221 | ||||||
| chr3:154217367
|
C | T | 12 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1846-502C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217367 | ||||||
| chr3:154217418
|
G | T | 1 | a0001c0001t0002g0260 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1846-451G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217418 | ||||||
| chr3:154217459
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1846-410C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217459 | ||||||
| chr3:154217460
|
G | A | 2 | a0001c0001t0023g0131a0005c0008t0023g0123 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1846-409G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217460 | ||||||
| chr3:154217542
|
A | T | 213 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1846-327A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217542 | ||||||
| chr3:154217631
|
C | T | 7 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1846-238C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217631 | ||||||
| chr3:154217685
|
A | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1846-184A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217685 | ||||||
| chr3:154217813
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1846-56G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154217813 | ||||||
| chr3:154217982
|
C | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1935+24C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154217982 | ||||||
| chr3:154218019
|
C | G | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1935+61C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154218019 | ||||||
| chr3:154218382
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+424G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154218382 | ||||||
| chr3:154218456
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+498T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154218456 | ||||||
| chr3:154218585
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1935+627C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154218585 | ||||||
| chr3:154218912
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+954G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154218912 | ||||||
| chr3:154219202
|
T | C | 1 | a0001c0001t0010g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1935+1244T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219202 | ||||||
| chr3:154219393
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0179 | 2 | NA18942.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1935+1435G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219393 | ||||||
| chr3:154219488
|
G | A | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0039g0275 | 3 | HG02886.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1935+1530G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219488 | ||||||
| chr3:154219537
|
T | C | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+1579T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219537 | ||||||
| chr3:154219590
|
T | TA | 8 | a0001c0001t0004g0209a0001c0001t0004g0210a0001c0001t0004g0211others(5): Show | 8 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+1645dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154219590 | |||||
| chr3:154219599
|
A | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0234a0001c0001t0004g0137others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+1641A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219599 | ||||||
| chr3:154219664
|
C | T | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1935+1706C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219664 | ||||||
| chr3:154219709
|
C | T | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+1751C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219709 | ||||||
| chr3:154219782
|
C | T | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1935+1824C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219782 | ||||||
| chr3:154219788
|
C | T | 29 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0002g0213others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1935+1830C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219788 | ||||||
| chr3:154219846
|
G | A | 2 | a0002c0002t0006g0030a0002c0002t0006g0058 | 2 | NA18994.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1935+1888G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219846 | ||||||
| chr3:154219909
|
G | A | 2 | a0002c0002t0003g0051a0012c0010t0002g0241 | 2 | HG02602.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1935+1951G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219909 | ||||||
| chr3:154219913
|
C | CA | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1935+1963dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154219913 | |||||
| chr3:154219936
|
C | A | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1935+1978C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219936 | ||||||
| chr3:154219936
|
C | CAAACAAA others(3): Show |
2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+1979_1935+198 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154219936 | |||||
| chr3:154219939
|
A | ACAAAAAA others(3): Show |
262 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1935+1988_1935+198 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154219939 | |||||
| chr3:154219939
|
A | C | 1 | a0001c0001t0004g0278 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1935+1981A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219939 | ||||||
| chr3:154219940
|
C | CAAACAAA others(3): Show |
3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1935+1985_1935+198 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154219940 | |||||
| chr3:154219964
|
G | A | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1935+2006G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154219964 | ||||||
| chr3:154220602
|
G | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1935+2644G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154220602 | ||||||
| chr3:154220745
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1935+2787T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154220745 | ||||||
| chr3:154221039
|
C | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+3081C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221039 | ||||||
| chr3:154221146
|
C | CA | 47 | a0001c0001t0001g0204a0001c0001t0001g0268a0001c0001t0002g0142others(44): Show | 47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1935+3200dupA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154221146 | |||||
| chr3:154221152
|
A | C | 1 | a0002c0002t0003g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1935+3194A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221152 | ||||||
| chr3:154221310
|
A | G | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1935+3352A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221310 | ||||||
| chr3:154221440
|
T | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1935+3482T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221440 | ||||||
| chr3:154221495
|
T | C | 1 | a0002c0003t0025g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1935+3537T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221495 | ||||||
| chr3:154221869
|
T | G | 2 | a0002c0002t0003g0044a0002c0002t0027g0046 | 2 | NA18942.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1935+3911T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221869 | ||||||
| chr3:154221908
|
T | C | 1 | a0002c0003t0044g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1936-3948T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154221908 | ||||||
| chr3:154222251
|
T | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1936-3605T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222251 | ||||||
| chr3:154222294
|
A | G | 1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1936-3562A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222294 | ||||||
| chr3:154222352
|
G | A | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-3504G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222352 | ||||||
| chr3:154222385
|
A | G | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-3471A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222385 | ||||||
| chr3:154222414
|
C | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1936-3442C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222414 | ||||||
| chr3:154222770
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1936-3086T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222770 | ||||||
| chr3:154222999
|
T | A | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1936-2857T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154222999 | ||||||
| chr3:154223125
|
A | G | 5 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0217others(2): Show | 5 | HG02074.hp2 HG02132.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2731A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223125 | ||||||
| chr3:154223166
|
C | T | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-2690C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223166 | ||||||
| chr3:154223217
|
G | C | 3 | a0001c0001t0037g0256a0002c0007t0018g0090a0002c0007t0018g0091 | 3 | HG02145.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1936-2639G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223217 | ||||||
| chr3:154223371
|
T | C | 46 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(43): Show | 47 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1936-2485T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223371 | ||||||
| chr3:154223394
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0011g0002a0001c0001t0043g0134 | 3 | HG01069.hp2 HG01071.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1936-2462A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223394 | ||||||
| chr3:154223419
|
G | A | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1936-2437G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223419 | ||||||
| chr3:154223594
|
A | T | 210 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(207): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1936-2262A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223594 | ||||||
| chr3:154223663
|
A | G | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1936-2193A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223663 | ||||||
| chr3:154223882
|
T | G | 47 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(44): Show | 48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1936-1974T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223882 | ||||||
| chr3:154223975
|
GA | G | 207 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1936-1870delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154223975 | |||||
| chr3:154224278
|
C | T | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1936-1578C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224278 | ||||||
| chr3:154224302
|
A | G | 4 | a0001c0001t0002g0142a0001c0015t0002g0143a0002c0002t0024g0035others(1): Show | 4 | HG02071.hp2 HG02735.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1936-1554A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224302 | ||||||
| chr3:154224611
|
C | A | 44 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(41): Show | 44 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1936-1245C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224611 | ||||||
| chr3:154224780
|
T | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1936-1076T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224780 | ||||||
| chr3:154224886
|
C | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1936-970C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224886 | ||||||
| chr3:154224987
|
A | G | 2 | a0002c0002t0005g0042a0002c0002t0005g0043 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1936-869A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154224987 | ||||||
| chr3:154225057
|
TA | T | 115 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(112): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1936-788delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr3 | 154225057 | |||||
| chr3:154225219
|
G | T | 2 | a0002c0003t0018g0092a0002c0003t0046g0093 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1936-637G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225219 | ||||||
| chr3:154225279
|
C | A | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1936-577C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225279 | ||||||
| chr3:154225595
|
A | G | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-261A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225595 | ||||||
| chr3:154225780
|
G | A | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1936-76G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225780 | ||||||
| chr3:154225833
|
A | C | 3 | a0002c0002t0003g0047a0002c0002t0003g0049a0002c0002t0003g0054 | 3 | NA18612.hp2 NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1936-23A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225833 | ||||||
| chr3:154225838
|
G | A | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1936-18G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154225838 | ||||||
| chr3:154226208
|
A | G | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2090+198A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226208 | ||||||
| chr3:154226268
|
A | G | 2 | a0001c0001t0023g0131a0005c0008t0023g0123 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2090+258A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226268 | ||||||
| chr3:154226308
|
C | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2090+298C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226308 | ||||||
| chr3:154226338
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2090+328C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226338 | ||||||
| chr3:154226395
|
G | T | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2090+385G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226395 | ||||||
| chr3:154226431
|
C | T | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2090+421C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226431 | ||||||
| chr3:154226502
|
G | T | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2090+492G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226502 | ||||||
| chr3:154226617
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2090+607A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226617 | ||||||
| chr3:154226660
|
T | TAC | 8 | a0001c0001t0002g0226a0001c0001t0015g0124a0001c0001t0041g0165others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2090+685_2090+686d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACAC | 12 | a0001c0001t0010g0138a0001c0001t0010g0140a0001c0001t0011g0141others(9): Show | 12 | HG00323.hp1 HG00741.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2090+683_2090+686d others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACAC | 5 | a0001c0001t0001g0204a0001c0001t0002g0225a0001c0001t0002g0229others(2): Show | 6 | HG00140.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.2090+681_2090+686d others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACACA others(1): Show |
22 | a0001c0001t0002g0231a0001c0001t0002g0233a0001c0001t0002g0235others(19): Show | 22 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2090+679_2090+686d others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACACA others(3): Show |
10 | a0001c0001t0002g0152a0001c0001t0002g0191a0001c0001t0002g0203others(7): Show | 10 | HG00609.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2090+677_2090+686d others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACACA others(5): Show |
5 | a0001c0001t0002g0142a0001c0001t0002g0162a0001c0001t0029g0151others(2): Show | 5 | HG02071.hp2 HG02132.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2090+675_2090+686d others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0161a0001c0001t0002g0217 | 2 | HG02074.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2090+671_2090+686d others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
T | TACACACA others(11): Show |
2 | a0001c0001t0002g0259a0002c0003t0018g0092 | 2 | NA19009.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2090+669_2090+686d others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
TAC | T | 22 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0157others(19): Show | 22 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2090+685_2090+686d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226660
|
TACAC | T | 178 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2090+683_2090+686d others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154226660 | |||||
| chr3:154226695
|
A | C | 5 | a0001c0001t0010g0239a0001c0001t0013g0246a0004c0005t0013g0136others(2): Show | 5 | HG01243.hp1 HG01346.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090+685A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226695 | ||||||
| chr3:154226697
|
C | A | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2090+687C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226697 | ||||||
| chr3:154226719
|
A | G | 43 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(40): Show | 44 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2090+709A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226719 | ||||||
| chr3:154226982
|
T | G | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090+972T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154226982 | ||||||
| chr3:154227033
|
C | G | 17 | a0001c0001t0007g0206a0001c0001t0017g0132a0001c0001t0037g0256others(14): Show | 17 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090+1023C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227033 | ||||||
| chr3:154227166
|
A | G | 1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2090+1156A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227166 | ||||||
| chr3:154227292
|
AT | A | 246 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0153others(243): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2090+1303delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154227292 | |||||
| chr3:154227292
|
ATT | A | 15 | a0001c0001t0001g0146a0001c0001t0001g0185a0001c0001t0001g0194others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.2090+1302_2090+130 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154227292 | |||||
| chr3:154227464
|
G | A | 3 | a0002c0003t0003g0089a0002c0003t0005g0087a0002c0003t0006g0088 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2090+1454G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227464 | ||||||
| chr3:154227486
|
T | TC | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2090+1477dupC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154227486 | |||||
| chr3:154227509
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2090+1499C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227509 | ||||||
| chr3:154227580
|
C | T | 1 | a0001c0001t0037g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2090+1570C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227580 | ||||||
| chr3:154227625
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2090+1615G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227625 | ||||||
| chr3:154227673
|
T | G | 1 | a0001c0001t0007g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2090+1663T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227673 | ||||||
| chr3:154227706
|
G | A | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2090+1696G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227706 | ||||||
| chr3:154228136
|
A | AT | 118 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.2090+2142dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154228136 | |||||
| chr3:154228136
|
AT | A | 16 | a0001c0001t0002g0236a0001c0001t0007g0206a0001c0001t0017g0132others(13): Show | 16 | HG01169.hp1 HG01255.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2090+2142delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154228136 | |||||
| chr3:154228206
|
T | A | 1 | a0002c0003t0006g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2090+2196T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228206 | ||||||
| chr3:154228237
|
A | G | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090+2227A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228237 | ||||||
| chr3:154228278
|
C | T | 1 | a0002c0002t0052g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2090+2268C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228278 | ||||||
| chr3:154228280
|
G | A | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090+2270G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228280 | ||||||
| chr3:154228287
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2090+2277G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228287 | ||||||
| chr3:154228389
|
G | A | 3 | a0002c0002t0006g0027a0002c0002t0006g0029a0002c0002t0006g0063 | 3 | NA18946.hp2 NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2090+2379G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228389 | ||||||
| chr3:154228394
|
C | T | 1 | a0002c0002t0003g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2090+2384C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228394 | ||||||
| chr3:154228427
|
G | A | 1 | a0001c0001t0002g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2090+2417G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228427 | ||||||
| chr3:154228436
|
C | CT | 6 | a0001c0001t0010g0239a0001c0001t0013g0246a0002c0003t0006g0101others(3): Show | 6 | HG01243.hp1 HG01346.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2090+2439dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154228436 | |||||
| chr3:154228436
|
CT | C | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 45 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.2090+2439delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154228436 | |||||
| chr3:154228560
|
T | C | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2090+2550T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228560 | ||||||
| chr3:154228628
|
T | G | 213 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(210): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2090+2618T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228628 | ||||||
| chr3:154228633
|
C | T | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2090+2623C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228633 | ||||||
| chr3:154228674
|
C | G | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2090+2664C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228674 | ||||||
| chr3:154228696
|
T | G | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2090+2686T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228696 | ||||||
| chr3:154228713
|
C | T | 1 | a0002c0002t0003g0066 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2090+2703C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228713 | ||||||
| chr3:154228741
|
GA | G | 268 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2090+2733delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154228741 | |||||
| chr3:154228790
|
A | C | 1 | a0001c0001t0002g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2090+2780A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228790 | ||||||
| chr3:154228881
|
C | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2090+2871C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228881 | ||||||
| chr3:154228980
|
G | A | 1 | a0002c0002t0008g0032 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2090+2970G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228980 | ||||||
| chr3:154228987
|
G | A | 1 | a0001c0001t0007g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2090+2977G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154228987 | ||||||
| chr3:154229425
|
T | C | 1 | a0002c0003t0027g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2090+3415T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154229425 | ||||||
| chr3:154229430
|
G | C | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2090+3420G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154229430 | ||||||
| chr3:154229570
|
T | C | 81 | a0001c0001t0001g0201a0001c0001t0007g0144a0001c0001t0007g0160others(78): Show | 82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.2090+3560T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154229570 | ||||||
| chr3:154229773
|
A | G | 20 | a0001c0001t0001g0201a0002c0002t0005g0060a0002c0003t0005g0001others(17): Show | 21 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.2090+3763A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154229773 | ||||||
| chr3:154230181
|
TGTTA | T | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090+4175_2090+417 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154230181 | |||||
| chr3:154230230
|
G | A | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2090+4220G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154230230 | ||||||
| chr3:154230599
|
T | C | 1 | a0001c0001t0012g0263 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2090+4589T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154230599 | ||||||
| chr3:154230739
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2090+4729T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154230739 | ||||||
| chr3:154230836
|
A | G | 2 | a0001c0001t0002g0240a0001c0001t0002g0242 | 2 | NA19006.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2090+4826A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154230836 | ||||||
| chr3:154230946
|
A | G | 1 | a0002c0003t0003g0089 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2090+4936A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154230946 | ||||||
| chr3:154231201
|
G | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2090+5191G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231201 | ||||||
| chr3:154231254
|
C | T | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2090+5244C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231254 | ||||||
| chr3:154231509
|
A | G | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2090+5499A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231509 | ||||||
| chr3:154231589
|
G | GT | 279 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(276): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2090+5581dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154231589 | |||||
| chr3:154231654
|
G | GT | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2090+5649dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154231654 | |||||
| chr3:154231771
|
G | A | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2090+5761G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231771 | ||||||
| chr3:154231876
|
CAT | C | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2090+5867_2090+586 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231876 | ||||||
| chr3:154231899
|
GT | G | 51 | a0001c0001t0001g0177a0001c0001t0001g0204a0001c0001t0002g0142others(48): Show | 52 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.2090+5903delT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154231899 | |||||
| chr3:154231913
|
T | G | 257 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2090+5903T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231913 | ||||||
| chr3:154231913
|
T | TG | 11 | a0001c0001t0004g0209a0001c0001t0007g0182a0001c0001t0015g0124others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2090+5903_2090+590 others(5): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231913 | ||||||
| chr3:154231924
|
A | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2090+5914A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231924 | ||||||
| chr3:154232005
|
G | A | 1 | a0002c0002t0008g0032 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2090+5995G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232005 | ||||||
| chr3:154232176
|
T | G | 4 | a0001c0001t0010g0140a0001c0001t0011g0141a0003c0004t0010g0013others(1): Show | 4 | HG00741.hp2 HG01099.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090+6166T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232176 | ||||||
| chr3:154232186
|
A | G | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2090+6176A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232186 | ||||||
| chr3:154232384
|
ATGTT | A | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2090+6379_2090+638 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154232384 | |||||
| chr3:154232544
|
T | C | 1 | a0002c0002t0003g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2090+6534T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232544 | ||||||
| chr3:154232682
|
A | G | 45 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(42): Show | 46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2090+6672A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232682 | ||||||
| chr3:154232915
|
A | C | 47 | a0001c0001t0001g0204a0001c0001t0002g0142a0001c0001t0002g0152others(44): Show | 48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.2090+6905A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232915 | ||||||
| chr3:154232951
|
C | T | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2090+6941C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232951 | ||||||
| chr3:154233021
|
C | T | 2 | a0001c0001t0021g0133a0005c0008t0014g0122 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2090+7011C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233021 | ||||||
| chr3:154233107
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2090+7097A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233107 | ||||||
| chr3:154233179
|
C | A | 2 | a0001c0001t0004g0214a0001c0001t0004g0215 | 2 | NA18965.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2090+7169C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233179 | ||||||
| chr3:154233296
|
A | T | 13 | a0001c0001t0007g0206a0001c0001t0017g0132a0001c0001t0037g0256others(10): Show | 13 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2091-7074A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233296 | ||||||
| chr3:154233297
|
T | A | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-7073T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233297 | ||||||
| chr3:154233395
|
G | T | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2091-6975G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233395 | ||||||
| chr3:154233459
|
C | T | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2091-6911C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233459 | ||||||
| chr3:154233585
|
G | A | 2 | a0002c0003t0018g0092a0002c0003t0046g0093 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2091-6785G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233585 | ||||||
| chr3:154233712
|
A | G | 1 | a0001c0001t0009g0261 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2091-6658A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233712 | ||||||
| chr3:154233902
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2091-6468C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233902 | ||||||
| chr3:154233930
|
A | G | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2091-6440A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154233930 | ||||||
| chr3:154234155
|
G | A | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2091-6215G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234155 | ||||||
| chr3:154234312
|
C | T | 1 | a0002c0003t0005g0116 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2091-6058C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234312 | ||||||
| chr3:154234541
|
T | A | 5 | a0001c0001t0010g0239a0001c0001t0013g0246a0004c0005t0013g0136others(2): Show | 5 | HG01243.hp1 HG01346.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-5829T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234541 | ||||||
| chr3:154234564
|
C | T | 1 | a0001c0001t0007g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2091-5806C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234564 | ||||||
| chr3:154234685
|
T | G | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2091-5685T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234685 | ||||||
| chr3:154234834
|
C | T | 6 | a0001c0001t0017g0132a0001c0001t0037g0256a0002c0007t0018g0090others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2091-5536C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234834 | ||||||
| chr3:154234839
|
C | T | 52 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(49): Show | 52 | HG00558.hp2 HG00597.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.2091-5531C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234839 | ||||||
| chr3:154234851
|
C | T | 1 | a0001c0001t0043g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2091-5519C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234851 | ||||||
| chr3:154234875
|
T | C | 1 | a0007c0006t0017g0129 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2091-5495T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234875 | ||||||
| chr3:154234883
|
A | T | 1 | a0001c0001t0034g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2091-5487A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234883 | ||||||
| chr3:154234913
|
T | C | 14 | a0001c0001t0001g0173a0001c0001t0007g0220a0001c0001t0012g0178others(11): Show | 14 | HG01123.hp2 HG01346.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2091-5457T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234913 | ||||||
| chr3:154234914
|
C | T | 3 | a0001c0001t0007g0220a0002c0002t0028g0077a0002c0002t0028g0078 | 3 | HG01123.hp2 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2091-5456C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234914 | ||||||
| chr3:154234915
|
A | G | 9 | a0001c0001t0007g0220a0001c0001t0012g0178a0001c0001t0021g0133others(6): Show | 9 | HG01123.hp2 HG01346.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2091-5455A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234915 | ||||||
| chr3:154234920
|
C | T | 60 | a0001c0001t0001g0167a0001c0001t0001g0201a0001c0001t0001g0207others(57): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.2091-5450C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234920 | ||||||
| chr3:154234921
|
G | A | 7 | a0001c0001t0001g0173a0001c0001t0007g0220a0001c0001t0012g0178others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091-5449G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234921 | ||||||
| chr3:154234923
|
G | A | 1 | a0002c0002t0006g0029 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2091-5447G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234923 | ||||||
| chr3:154234926
|
C | T | 1 | a0002c0002t0006g0029 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2091-5444C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234926 | ||||||
| chr3:154234931
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2091-5439A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234931 | ||||||
| chr3:154234964
|
G | A | 5 | a0001c0001t0007g0206a0001c0001t0036g0205a0002c0003t0003g0098others(2): Show | 5 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-5406G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234964 | ||||||
| chr3:154234970
|
T | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0012g0178others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091-5400T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234970 | ||||||
| chr3:154234984
|
G | T | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2091-5386G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154234984 | ||||||
| chr3:154235008
|
C | T | 3 | a0001c0001t0043g0134a0002c0003t0018g0092a0002c0003t0046g0093 | 3 | HG03579.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2091-5362C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235008 | ||||||
| chr3:154235059
|
C | A | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2091-5311C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235059 | ||||||
| chr3:154235112
|
G | T | 7 | a0001c0001t0001g0204a0001c0001t0017g0132a0001c0001t0037g0256others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091-5258G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235112 | ||||||
| chr3:154235126
|
A | C | 3 | a0001c0001t0017g0132a0007c0006t0017g0128a0007c0006t0017g0129 | 3 | HG01884.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2091-5244A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235126 | ||||||
| chr3:154235329
|
A | T | 160 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.2091-5041A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235329 | ||||||
| chr3:154235336
|
TGTGGGTT others(10): Show |
T | 3 | a0001c0001t0001g0167a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | NA18947.hp2 NA18960.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2091-5016_2091-500 others(21): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154235336 | |||||
| chr3:154235373
|
A | C | 20 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(17): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2091-4997A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235373 | ||||||
| chr3:154235472
|
T | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2091-4898T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235472 | ||||||
| chr3:154235603
|
G | A | 8 | a0001c0001t0017g0132a0001c0001t0037g0256a0002c0003t0048g0097others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2091-4767G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235603 | ||||||
| chr3:154235651
|
G | A | 112 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.2091-4719G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154235651 | ||||||
| chr3:154236053
|
G | A | 7 | a0001c0001t0007g0206a0001c0001t0007g0274a0001c0001t0036g0205others(4): Show | 7 | HG01069.hp1 HG01255.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091-4317G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236053 | ||||||
| chr3:154236150
|
C | T | 1 | a0002c0003t0044g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2091-4220C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236150 | ||||||
| chr3:154236413
|
G | C | 1 | a0009c0016t0001g0218 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2091-3957G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236413 | ||||||
| chr3:154236422
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | NA18947.hp2 NA18960.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-3948T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236422 | ||||||
| chr3:154236692
|
C | T | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2091-3678C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236692 | ||||||
| chr3:154236726
|
T | G | 1 | a0001c0001t0002g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2091-3644T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236726 | ||||||
| chr3:154236846
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2091-3524A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236846 | ||||||
| chr3:154236964
|
G | A | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2091-3406G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154236964 | ||||||
| chr3:154237513
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0189 | 3 | HG00738.hp1 HG01123.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2091-2857G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154237513 | ||||||
| chr3:154237538
|
T | TCA | 21 | a0001c0001t0002g0242a0001c0001t0002g0249a0001c0001t0004g0149others(18): Show | 21 | HG00621.hp2 HG01243.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.2091-2798_2091-279 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACA | 14 | a0001c0001t0002g0240a0001c0001t0004g0139a0001c0001t0004g0219others(11): Show | 15 | HG00140.hp1 HG00323.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.2091-2800_2091-279 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACA | 35 | a0001c0001t0001g0176a0001c0001t0001g0187a0001c0001t0001g0201others(32): Show | 36 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2091-2802_2091-279 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACAC others(1): Show |
79 | a0001c0001t0001g0181a0001c0001t0001g0204a0001c0001t0001g0222others(76): Show | 80 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.2091-2804_2091-279 others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACAC others(3): Show |
58 | a0001c0001t0001g0153a0001c0001t0001g0174a0001c0001t0001g0179others(55): Show | 59 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.2091-2806_2091-279 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACAC others(5): Show |
24 | a0001c0001t0001g0130a0001c0001t0001g0156a0001c0001t0001g0157others(21): Show | 24 | HG00099.hp2 HG01099.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.2091-2808_2091-279 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACAC others(7): Show |
13 | a0001c0001t0001g0150a0001c0001t0001g0177a0001c0001t0001g0199others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.2091-2810_2091-279 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
T | TCACACAC others(9): Show |
6 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0194others(3): Show | 6 | HG02015.hp2 HG02165.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091-2812_2091-279 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
TCA | T | 4 | a0001c0001t0001g0188a0001c0001t0002g0152a0001c0001t0014g0276others(1): Show | 4 | HG01175.hp2 HG02886.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091-2798_2091-279 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237538
|
TCACA | T | 4 | a0001c0001t0014g0277a0002c0003t0006g0115a0005c0008t0014g0122others(1): Show | 4 | HG02602.hp2 HG03098.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-2800_2091-279 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237538 | |||||
| chr3:154237572
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2091-2797_2091-279 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154237572 | |||||
| chr3:154237580
|
A | G | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2091-2790A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154237580 | ||||||
| chr3:154238118
|
T | A | 63 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(60): Show | 63 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.2091-2252T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238118 | ||||||
| chr3:154238161
|
C | T | 183 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2091-2209C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238161 | ||||||
| chr3:154238863
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2091-1507A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238863 | ||||||
| chr3:154238936
|
G | A | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2091-1434G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238936 | ||||||
| chr3:154238948
|
A | G | 53 | a0001c0001t0002g0002a0001c0001t0002g0142a0001c0001t0002g0152others(50): Show | 55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.2091-1422A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238948 | ||||||
| chr3:154239023
|
A | G | 184 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2091-1347A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239023 | ||||||
| chr3:154239068
|
T | G | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2091-1302T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239068 | ||||||
| chr3:154239069
|
T | C | 4 | a0002c0003t0005g0087a0002c0003t0006g0088a0002c0003t0006g0096others(1): Show | 4 | HG01433.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091-1301T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239069 | ||||||
| chr3:154239249
|
C | CGA | 10 | a0001c0001t0007g0144a0001c0001t0007g0175a0001c0001t0007g0182others(7): Show | 10 | HG01496.hp1 HG01993.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2091-1111_2091-111 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239249 | |||||
| chr3:154239249
|
CGA | C | 139 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0153others(136): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2091-1111_2091-111 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239249 | |||||
| chr3:154239249
|
CGAGAGAG others(5): Show |
C | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2091-1109_2091-109 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239249 | |||||
| chr3:154239251
|
AGAGAGAG others(3): Show |
A | 2 | a0001c0001t0035g0255a0002c0003t0027g0104 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2091-1109_2091-110 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239251 | |||||
| chr3:154239255
|
AGAGAGG | A | 5 | a0001c0001t0007g0274a0001c0001t0041g0165a0001c0009t0022g0163others(2): Show | 5 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-1109_2091-110 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239255 | |||||
| chr3:154239257
|
AGAG | A | 3 | a0001c0001t0001g0156a0002c0003t0005g0113a0002c0003t0006g0088 | 3 | HG00408.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2091-1111_2091-110 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239257 | |||||
| chr3:154239257
|
AGAGG | A | 8 | a0001c0001t0021g0133a0002c0002t0003g0038a0002c0002t0003g0064others(5): Show | 8 | HG01099.hp1 HG01123.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.2091-1109_2091-110 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239257 | |||||
| chr3:154239259
|
A | G | 51 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0001g0192others(48): Show | 51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2091-1111A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239259 | ||||||
| chr3:154239259
|
AGG | A | 10 | a0001c0001t0007g0206a0001c0001t0007g0216a0001c0001t0007g0220others(7): Show | 10 | HG01255.hp1 HG01346.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2091-1109_2091-110 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239259 | |||||
| chr3:154239261
|
G | A | 73 | a0001c0001t0001g0173a0001c0001t0001g0185a0001c0001t0001g0192others(70): Show | 73 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2091-1109G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239261 | ||||||
| chr3:154239261
|
G | GGA | 5 | a0001c0001t0010g0239a0003c0004t0010g0009a0003c0004t0010g0013others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-1071_2091-107 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239261 | |||||
| chr3:154239261
|
GGAGAGAG others(3): Show |
G | 1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2091-1079_2091-107 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239261 | |||||
| chr3:154239261
|
GGAGAGAG others(5): Show |
G | 2 | a0001c0001t0014g0276a0001c0001t0014g0277 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2091-1081_2091-107 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239261 | |||||
| chr3:154239263
|
A | G | 35 | a0001c0001t0007g0160a0001c0001t0007g0172a0001c0001t0021g0212others(32): Show | 35 | HG00558.hp2 HG01081.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.2091-1107A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239263 | ||||||
| chr3:154239265
|
A | G | 10 | a0001c0001t0007g0206a0001c0001t0007g0216a0001c0001t0007g0220others(7): Show | 10 | HG01255.hp1 HG01346.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2091-1105A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239265 | ||||||
| chr3:154239267
|
A | G | 9 | a0001c0001t0021g0133a0002c0002t0003g0038a0002c0002t0003g0064others(6): Show | 9 | HG01099.hp1 HG01123.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.2091-1103A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239267 | ||||||
| chr3:154239269
|
A | G | 5 | a0001c0001t0007g0274a0001c0001t0041g0165a0001c0009t0022g0163others(2): Show | 5 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-1101A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239269 | ||||||
| chr3:154239271
|
A | G | 4 | a0001c0001t0036g0205a0001c0001t0041g0165a0001c0009t0022g0163others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-1099A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239271 | ||||||
| chr3:154239273
|
A | G | 5 | a0001c0001t0035g0255a0001c0001t0041g0165a0001c0009t0022g0163others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2091-1097A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239273 | ||||||
| chr3:154239275
|
A | G | 1 | a0006c0012t0008g0018 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2091-1095A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239275 | ||||||
| chr3:154239285
|
AGAGAGAG others(17): Show |
A | 1 | a0001c0001t0002g0217 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2091-1083_2091-106 others(28): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239285 | |||||
| chr3:154239287
|
A | T | 1 | a0002c0002t0049g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2091-1083A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239287 | ||||||
| chr3:154239287
|
AGAGAGAG others(7): Show |
A | 1 | a0002c0003t0046g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2091-1081_2091-106 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239287 | |||||
| chr3:154239287
|
AGAGAGAG others(9): Show |
A | 1 | a0002c0003t0018g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2091-1081_2091-106 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239287 | |||||
| chr3:154239287
|
AGAGAGAG others(11): Show |
A | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2091-1081_2091-106 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239287 | |||||
| chr3:154239287
|
AGAGAGAG others(13): Show |
A | 1 | a0001c0001t0020g0003 | 2 | HG00140.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2091-1081_2091-106 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239287 | |||||
| chr3:154239287
|
AGAGAGAG others(17): Show |
A | 2 | a0001c0001t0001g0167a0001c0001t0002g0162 | 2 | HG02132.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2091-1081_2091-105 others(28): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239287 | |||||
| chr3:154239289
|
A | AGTGT | 4 | a0001c0001t0007g0172a0002c0002t0003g0045a0002c0002t0003g0083others(1): Show | 4 | HG02155.hp1 NA18947.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-1080_2091-107 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
A | T | 8 | a0001c0001t0007g0175a0001c0001t0007g0220a0001c0001t0021g0212others(5): Show | 8 | HG01346.hp1 HG01496.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2091-1081A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239289 | ||||||
| chr3:154239289
|
AGAGAGAG others(7): Show |
A | 1 | a0002c0007t0018g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2091-1079_2091-106 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
AGAGAGAG others(9): Show |
A | 1 | a0002c0003t0050g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2091-1079_2091-106 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
AGAGAGAG others(11): Show |
A | 2 | a0001c0001t0037g0256a0002c0007t0018g0091 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2091-1079_2091-106 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
AGAGAGAG others(13): Show |
A | 2 | a0001c0001t0002g0224a0003c0004t0002g0007 | 2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2091-1079_2091-106 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
AGAGAGAG others(15): Show |
A | 42 | a0001c0001t0002g0002a0001c0001t0002g0142a0001c0001t0002g0152others(39): Show | 43 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2091-1079_2091-105 others(26): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239289
|
AGAGAGAG others(19): Show |
A | 1 | a0001c0001t0002g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2091-1079_2091-105 others(30): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239289 | |||||
| chr3:154239291
|
A | AGTGTGT | 4 | a0002c0002t0003g0049a0002c0002t0003g0071a0002c0002t0003g0075others(1): Show | 4 | NA18978.hp2 NA18999.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-1078_2091-107 others(10): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239291
|
A | T | 32 | a0001c0001t0007g0144a0001c0001t0007g0172a0001c0001t0007g0175others(29): Show | 32 | HG00558.hp2 HG01081.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.2091-1079A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239291 | ||||||
| chr3:154239291
|
AGAGAGAG others(7): Show |
A | 1 | a0001c0001t0017g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2091-1077_2091-106 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239291
|
AGAGAGAG others(9): Show |
A | 2 | a0007c0006t0017g0128a0007c0006t0017g0129 | 2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2091-1077_2091-106 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239291
|
AGAGAGAG others(11): Show |
A | 1 | a0001c0001t0004g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2091-1077_2091-106 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239291
|
AGAGAGAG others(13): Show |
A | 3 | a0001c0001t0002g0273a0001c0001t0009g0267a0001c0001t0016g0186 | 3 | HG01975.hp1 NA18946.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2091-1077_2091-105 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239291
|
AGAGAGAG others(15): Show |
A | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | NA18948.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2091-1077_2091-105 others(26): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239291 | |||||
| chr3:154239293
|
A | AGTGTGTG others(3): Show |
2 | a0002c0002t0003g0076a0002c0002t0008g0081 | 2 | NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2091-1076_2091-107 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239293 | |||||
| chr3:154239293
|
A | T | 46 | a0001c0001t0007g0144a0001c0001t0007g0172a0001c0001t0007g0175others(43): Show | 46 | HG00558.hp2 HG01081.hp1 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.2091-1077A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239293 | ||||||
| chr3:154239293
|
AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0007g0160 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2091-1075_2091-106 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239293 | |||||
| chr3:154239293
|
AGAGAGAG others(9): Show |
A | 3 | a0001c0001t0004g0257a0001c0001t0004g0266a0002c0003t0048g0097 | 3 | HG02622.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2091-1075_2091-106 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239293 | |||||
| chr3:154239293
|
AGAGAGAG others(11): Show |
A | 3 | a0001c0001t0004g0278a0001c0001t0034g0202a0002c0003t0006g0115 | 3 | HG00544.hp2 NA18950.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2091-1075_2091-105 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239293 | |||||
| chr3:154239295
|
A | T | 60 | a0001c0001t0007g0144a0001c0001t0007g0172a0001c0001t0007g0175others(57): Show | 60 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.2091-1075A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239295 | ||||||
| chr3:154239295
|
AGAGAGTG others(5): Show |
A | 1 | a0002c0003t0044g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2091-1073_2091-106 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239295 | |||||
| chr3:154239295
|
AGAGAGTG others(9): Show |
A | 5 | a0001c0001t0001g0130a0001c0001t0001g0269a0001c0001t0004g0155others(2): Show | 5 | HG00544.hp1 HG01891.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-1073_2091-105 others(20): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239295 | |||||
| chr3:154239295
|
AGAGAGTG others(11): Show |
A | 1 | a0002c0003t0019g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2091-1073_2091-105 others(22): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239295 | |||||
| chr3:154239295
|
AGAGAGTG others(13): Show |
A | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2091-1073_2091-105 others(24): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239295 | |||||
| chr3:154239297
|
A | T | 65 | a0001c0001t0007g0144a0001c0001t0007g0172a0001c0001t0007g0175others(62): Show | 65 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.2091-1073A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239297 | ||||||
| chr3:154239297
|
AGAGTGTG others(5): Show |
A | 16 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0179others(13): Show | 17 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.2091-1071_2091-106 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239297 | |||||
| chr3:154239297
|
AGAGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0252a0001c0001t0004g0137a0002c0002t0005g0028others(1): Show | 4 | HG00099.hp1 HG01884.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-1071_2091-105 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239297 | |||||
| chr3:154239299
|
A | T | 69 | a0001c0001t0007g0144a0001c0001t0007g0172a0001c0001t0007g0175others(66): Show | 69 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(66): Show |
intron_variant | MODIFIER | c.2091-1071A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239299 | ||||||
| chr3:154239299
|
AGTGTGTG others(1): Show |
A | 13 | a0001c0001t0001g0146a0001c0001t0004g0139a0001c0001t0004g0209others(10): Show | 13 | HG00323.hp1 HG00408.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.2091-1036_2091-102 others(12): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239299 | |||||
| chr3:154239299
|
AGTGTGTG others(3): Show |
A | 24 | a0001c0001t0001g0156a0001c0001t0001g0181a0001c0001t0001g0188others(21): Show | 24 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2091-1038_2091-102 others(14): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239299 | |||||
| chr3:154239299
|
AGTGTGTG others(5): Show |
A | 57 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0157others(54): Show | 58 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2091-1040_2091-102 others(16): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239299 | |||||
| chr3:154239299
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2091-1042_2091-102 others(18): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | 154239299 | |||||
| chr3:154239301
|
T | A | 4 | a0001c0001t0010g0138a0002c0003t0006g0088a0003c0004t0010g0009others(1): Show | 4 | HG01099.hp2 HG01106.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091-1069T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239301 | ||||||
| chr3:154239302
|
G | A | 1 | a0005c0008t0014g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2091-1068G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239302 | ||||||
| chr3:154239303
|
T | A | 2 | a0001c0001t0010g0140a0002c0003t0006g0088 | 2 | HG03239.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2091-1067T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239303 | ||||||
| chr3:154239304
|
G | A | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2091-1066G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239304 | ||||||
| chr3:154239305
|
T | A | 1 | a0002c0003t0006g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2091-1065T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239305 | ||||||
| chr3:154239306
|
G | A | 2 | a0001c0001t0014g0276a0001c0001t0014g0277 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2091-1064G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239306 | ||||||
| chr3:154239307
|
T | A | 1 | a0002c0003t0006g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2091-1063T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239307 | ||||||
| chr3:154239309
|
T | A | 4 | a0001c0001t0001g0146a0001c0001t0004g0139a0001c0001t0012g0178others(1): Show | 4 | HG00408.hp2 HG01109.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-1061T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239309 | ||||||
| chr3:154239311
|
T | A | 9 | a0001c0001t0001g0156a0001c0001t0001g0200a0001c0001t0033g0221others(6): Show | 9 | HG00408.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2091-1059T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239311 | ||||||
| chr3:154239313
|
T | A | 2 | a0002c0003t0005g0121a0002c0003t0006g0100 | 2 | NA18948.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2091-1057T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239313 | ||||||
| chr3:154239330
|
G | T | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2091-1040G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239330 | ||||||
| chr3:154239401
|
C | T | 64 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.2091-969C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239401 | ||||||
| chr3:154239471
|
T | C | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2091-899T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239471 | ||||||
| chr3:154239551
|
C | T | 67 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(64): Show | 67 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.2091-819C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239551 | ||||||
| chr3:154239812
|
G | A | 1 | a0002c0003t0003g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2091-558G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239812 | ||||||
| chr3:154239953
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2091-417G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239953 | ||||||
| chr3:154239997
|
T | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG02132.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2091-373T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239997 | ||||||
| chr3:154240062
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2091-308A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240062 | ||||||
| chr3:154240179
|
T | C | 3 | a0001c0001t0009g0004a0001c0001t0009g0261a0002c0003t0025g0105 | 4 | HG02280.hp1 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2091-191T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240179 | ||||||
| chr3:154240272
|
C | G | 2 | a0002c0003t0005g0135a0002c0003t0026g0103 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2091-98C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240272 | ||||||
| chr3:154240288
|
C | G | 6 | a0002c0002t0005g0034a0002c0002t0005g0042a0002c0002t0005g0043others(3): Show | 6 | HG01243.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2091-82C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240288 | ||||||
| chr3:154240304
|
C | T | 1 | a0008c0017t0002g0170 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2091-66C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240304 | ||||||
| chr3:154240316
|
A | G | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2091-54A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240316 | ||||||
| chr3:154240356
|
C | G | 2 | a0002c0002t0003g0061a0011c0018t0007g0006 | 2 | HG01496.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2091-14C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154240356 | ||||||
| chr3:154240665
|
G | T | 1 | a0002c0003t0006g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2300+86G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154240665 | ||||||
| chr3:154241053
|
T | A | 2 | a0001c0001t0021g0133a0001c0001t0035g0255 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2300+474T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241053 | ||||||
| chr3:154241087
|
C | A | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2300+508C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241087 | ||||||
| chr3:154241239
|
G | T | 185 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(182): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2300+660G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241239 | ||||||
| chr3:154241433
|
C | G | 1 | a0001c0001t0010g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2300+854C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241433 | ||||||
| chr3:154241495
|
G | A | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2300+916G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241495 | ||||||
| chr3:154241565
|
C | T | 11 | a0001c0001t0017g0132a0001c0001t0037g0256a0002c0003t0018g0092others(8): Show | 11 | HG01884.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2300+986C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241565 | ||||||
| chr3:154241566
|
G | A | 1 | a0001c0001t0014g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2300+987G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241566 | ||||||
| chr3:154241628
|
C | T | 1 | a0001c0001t0010g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2300+1049C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241628 | ||||||
| chr3:154241791
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2300+1212G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241791 | ||||||
| chr3:154241832
|
G | A | 1 | a0001c0001t0002g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2300+1253G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241832 | ||||||
| chr3:154242300
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2300+1721C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154242300 | ||||||
| chr3:154242680
|
C | G | 1 | a0002c0003t0045g0095 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2300+2101C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154242680 | ||||||
| chr3:154242819
|
CA | C | 6 | a0001c0001t0014g0276a0001c0001t0014g0277a0002c0003t0018g0092others(3): Show | 6 | HG02886.hp1 HG03098.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.2300+2250delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154242819 | |||||
| chr3:154243782
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2300+3203T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154243782 | ||||||
| chr3:154243824
|
AAT | A | 3 | a0001c0001t0009g0004a0001c0001t0009g0261a0002c0003t0025g0105 | 4 | HG02280.hp1 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2300+3250_2300+325 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154243824 | |||||
| chr3:154243838
|
C | G | 185 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(182): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2300+3259C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154243838 | ||||||
| chr3:154243870
|
A | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2300+3291A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154243870 | ||||||
| chr3:154244133
|
A | G | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2300+3554A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244133 | ||||||
| chr3:154244241
|
A | G | 3 | a0001c0001t0009g0004a0001c0001t0009g0261a0002c0003t0025g0105 | 4 | HG02280.hp1 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2300+3662A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244241 | ||||||
| chr3:154244339
|
C | T | 3 | a0001c0001t0007g0172a0002c0002t0003g0064a0002c0002t0003g0084 | 3 | HG02155.hp1 NA18945.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2300+3760C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244339 | ||||||
| chr3:154244561
|
G | A | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2300+3982G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244561 | ||||||
| chr3:154244684
|
C | T | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2300+4105C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244684 | ||||||
| chr3:154244736
|
ACT | A | 70 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(67): Show | 70 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.2300+4163_2300+416 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154244736 | |||||
| chr3:154244873
|
C | T | 1 | a0001c0001t0021g0133 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2300+4294C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154244873 | ||||||
| chr3:154244912
|
T | TTGC | 70 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(67): Show | 70 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.2300+4338_2300+434 others(7): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154244912 | |||||
| chr3:154245022
|
T | C | 4 | a0001c0001t0007g0206a0001c0001t0007g0274a0002c0003t0003g0089others(1): Show | 4 | HG01069.hp1 HG01255.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2300+4443T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245022 | ||||||
| chr3:154245070
|
G | A | 1 | a0001c0001t0004g0147 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2300+4491G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245070 | ||||||
| chr3:154245184
|
T | C | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2300+4605T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245184 | ||||||
| chr3:154245185
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2300+4606G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245185 | ||||||
| chr3:154245229
|
T | C | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2300+4650T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245229 | ||||||
| chr3:154245331
|
A | T | 1 | a0001c0001t0004g0248 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2300+4752A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245331 | ||||||
| chr3:154245336
|
G | A | 5 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0021g0133others(2): Show | 5 | HG02717.hp2 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2300+4757G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245336 | ||||||
| chr3:154245459
|
G | C | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2300+4880G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245459 | ||||||
| chr3:154245527
|
C | T | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2300+4948C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245527 | ||||||
| chr3:154245635
|
G | A | 1 | a0001c0001t0004g0148 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2300+5056G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245635 | ||||||
| chr3:154245683
|
T | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2300+5104T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245683 | ||||||
| chr3:154245773
|
A | G | 7 | a0002c0002t0003g0026a0002c0002t0003g0071a0002c0002t0003g0073others(4): Show | 7 | HG02015.hp1 NA18944.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2300+5194A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245773 | ||||||
| chr3:154245936
|
A | C | 1 | a0002c0003t0005g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2300+5357A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154245936 | ||||||
| chr3:154246119
|
G | A | 1 | a0002c0002t0005g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2300+5540G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246119 | ||||||
| chr3:154246184
|
T | C | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2300+5605T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246184 | ||||||
| chr3:154246214
|
C | T | 1 | a0002c0002t0006g0058 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2300+5635C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246214 | ||||||
| chr3:154246612
|
A | G | 2 | a0001c0001t0004g0257a0001c0001t0004g0266 | 2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2300+6033A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246612 | ||||||
| chr3:154246707
|
G | T | 130 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2300+6128G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246707 | ||||||
| chr3:154246740
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2300+6161A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246740 | ||||||
| chr3:154246785
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2300+6206A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246785 | ||||||
| chr3:154246856
|
T | C | 1 | a0002c0002t0003g0066 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2301-6260T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246856 | ||||||
| chr3:154246975
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-6141G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246975 | ||||||
| chr3:154246996
|
C | T | 4 | a0002c0003t0005g0087a0002c0003t0006g0088a0002c0003t0006g0096others(1): Show | 4 | HG01433.hp1 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-6120C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154246996 | ||||||
| chr3:154247003
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-6113G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247003 | ||||||
| chr3:154247158
|
C | T | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2301-5958C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247158 | ||||||
| chr3:154247279
|
A | G | 53 | a0001c0001t0002g0002a0001c0001t0002g0142a0001c0001t0002g0152others(50): Show | 55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.2301-5837A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247279 | ||||||
| chr3:154247518
|
C | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-5598C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247518 | ||||||
| chr3:154247518
|
C | T | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2301-5598C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247518 | ||||||
| chr3:154247623
|
CTCTA | C | 64 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.2301-5489_2301-548 others(8): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154247623 | |||||
| chr3:154247743
|
A | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2301-5373A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247743 | ||||||
| chr3:154247801
|
A | G | 1 | a0001c0001t0007g0175 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2301-5315A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247801 | ||||||
| chr3:154247881
|
G | A | 4 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0035g0255others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-5235G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154247881 | ||||||
| chr3:154248065
|
TC | T | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2301-5049delC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154248065 | |||||
| chr3:154248255
|
G | C | 53 | a0001c0001t0002g0002a0001c0001t0002g0142a0001c0001t0002g0152others(50): Show | 55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.2301-4861G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248255 | ||||||
| chr3:154248265
|
G | C | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2301-4851G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248265 | ||||||
| chr3:154248383
|
A | G | 1 | a0001c0001t0016g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2301-4733A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248383 | ||||||
| chr3:154248610
|
T | C | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2301-4506T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248610 | ||||||
| chr3:154248844
|
A | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2301-4272A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248844 | ||||||
| chr3:154248890
|
G | T | 1 | a0002c0002t0003g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2301-4226G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154248890 | ||||||
| chr3:154248989
|
C | CT | 4 | a0001c0001t0007g0144a0002c0002t0003g0037a0002c0002t0003g0038others(1): Show | 4 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-4124dupT | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154248989 | |||||
| chr3:154249224
|
T | A | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2301-3892T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249224 | ||||||
| chr3:154249294
|
A | G | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2301-3822A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249294 | ||||||
| chr3:154249358
|
A | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2301-3758A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249358 | ||||||
| chr3:154249509
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-3607G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249509 | ||||||
| chr3:154249514
|
T | C | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2301-3602T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249514 | ||||||
| chr3:154249519
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2301-3597A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249519 | ||||||
| chr3:154249661
|
C | G | 2 | a0002c0003t0004g0085a0002c0003t0004g0086 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2301-3455C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249661 | ||||||
| chr3:154249701
|
G | A | 64 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.2301-3415G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249701 | ||||||
| chr3:154249787
|
G | A | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2301-3329G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249787 | ||||||
| chr3:154249946
|
C | G | 2 | a0001c0001t0004g0147a0001c0001t0004g0148 | 2 | NA18979.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2301-3170C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249946 | ||||||
| chr3:154249974
|
T | C | 3 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093 | 3 | NA19030.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2301-3142T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154249974 | ||||||
| chr3:154250059
|
T | C | 2 | a0001c0001t0002g0240a0001c0001t0002g0242 | 2 | NA19006.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2301-3057T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250059 | ||||||
| chr3:154250087
|
A | G | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2301-3029A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250087 | ||||||
| chr3:154250097
|
C | G | 4 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093others(1): Show | 4 | HG03579.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-3019C>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250097 | ||||||
| chr3:154250117
|
G | A | 4 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093others(1): Show | 4 | HG03579.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-2999G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250117 | ||||||
| chr3:154250229
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2301-2887A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250229 | ||||||
| chr3:154250248
|
C | T | 1 | a0002c0002t0003g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2301-2868C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250248 | ||||||
| chr3:154250313
|
C | T | 19 | a0001c0001t0001g0201a0002c0002t0005g0060a0002c0003t0005g0001others(16): Show | 20 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.2301-2803C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250313 | ||||||
| chr3:154250384
|
A | G | 5 | a0001c0001t0010g0140a0001c0001t0010g0239a0003c0004t0010g0009others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2301-2732A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250384 | ||||||
| chr3:154250385
|
G | C | 2 | a0001c0001t0001g0207a0001c0001t0004g0208 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2301-2731G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250385 | ||||||
| chr3:154250387
|
G | A | 71 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(68): Show | 71 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.2301-2729G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250387 | ||||||
| chr3:154250550
|
T | C | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2301-2566T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250550 | ||||||
| chr3:154250616
|
C | T | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2301-2500C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250616 | ||||||
| chr3:154250752
|
C | T | 1 | a0002c0002t0008g0074 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2301-2364C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250752 | ||||||
| chr3:154250793
|
G | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2301-2323G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250793 | ||||||
| chr3:154250823
|
G | A | 4 | a0002c0003t0018g0092a0002c0003t0045g0095a0002c0003t0046g0093others(1): Show | 4 | HG03579.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-2293G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250823 | ||||||
| chr3:154250942
|
T | C | 1 | a0010c0011t0005g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2301-2174T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154250942 | ||||||
| chr3:154250962
|
TAG | T | 204 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.2301-2133_2301-213 others(6): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154250962 | |||||
| chr3:154251057
|
T | C | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2301-2059T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251057 | ||||||
| chr3:154251085
|
A | G | 2 | a0001c0001t0023g0131a0005c0008t0023g0123 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2301-2031A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251085 | ||||||
| chr3:154251213
|
G | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0176others(4): Show | 7 | NA18942.hp1 NA18947.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.2301-1903G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251213 | ||||||
| chr3:154251257
|
ATTTTC | A | 19 | a0001c0001t0001g0201a0002c0002t0005g0060a0002c0003t0005g0001others(16): Show | 20 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.2301-1853_2301-184 others(9): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154251257 | |||||
| chr3:154251290
|
T | C | 6 | a0001c0001t0004g0139a0001c0001t0004g0171a0001c0001t0004g0219others(3): Show | 6 | HG00099.hp2 HG00323.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2301-1826T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251290 | ||||||
| chr3:154251332
|
G | C | 4 | a0001c0001t0014g0276a0001c0001t0014g0277a0001c0001t0035g0255others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301-1784G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251332 | ||||||
| chr3:154251428
|
C | T | 1 | a0001c0001t0036g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2301-1688C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251428 | ||||||
| chr3:154251456
|
T | C | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2301-1660T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251456 | ||||||
| chr3:154251488
|
C | T | 86 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(83): Show | 86 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(83): Show |
intron_variant | MODIFIER | c.2301-1628C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251488 | ||||||
| chr3:154251647
|
T | C | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-1469T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251647 | ||||||
| chr3:154251672
|
G | C | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-1444G>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251672 | ||||||
| chr3:154251741
|
A | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-1375A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251741 | ||||||
| chr3:154251756
|
T | C | 1 | a0002c0002t0051g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2301-1360T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251756 | ||||||
| chr3:154251965
|
A | G | 4 | a0002c0002t0006g0030a0002c0002t0006g0048a0002c0002t0006g0058others(1): Show | 4 | HG00597.hp1 NA18954.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2301-1151A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251965 | ||||||
| chr3:154251985
|
C | T | 1 | a0002c0003t0005g0107 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2301-1131C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251985 | ||||||
| chr3:154251987
|
C | T | 3 | a0001c0001t0014g0276a0001c0001t0014g0277a0005c0008t0014g0122 | 3 | HG02886.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2301-1129C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154251987 | ||||||
| chr3:154252030
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2301-1086T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252030 | ||||||
| chr3:154252350
|
A | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2301-766A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252350 | ||||||
| chr3:154252373
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2301-743G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252373 | ||||||
| chr3:154252451
|
A | G | 1 | a0001c0001t0016g0264 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2301-665A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252451 | ||||||
| chr3:154252531
|
G | T | 1 | a0001c0001t0043g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2301-585G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252531 | ||||||
| chr3:154252688
|
G | A | 2 | a0001c0001t0002g0231a0001c0001t0002g0235 | 2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2301-428G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252688 | ||||||
| chr3:154252893
|
A | G | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2301-223A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252893 | ||||||
| chr3:154252915
|
CTT | C | 103 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(100): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2301-198_2301-197d others(4): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr3 | 154252915 | |||||
| chr3:154252997
|
A | G | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2301-119A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154252997 | ||||||
| chr3:154253007
|
A | G | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2301-109A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154253007 | ||||||
| chr3:154253013
|
T | A | 64 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.2301-103T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154253013 | ||||||
| chr3:154253483
|
G | A | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2368+300G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253483 | ||||||
| chr3:154253573
|
G | A | 64 | a0001c0001t0007g0144a0001c0001t0007g0160a0001c0001t0007g0172others(61): Show | 64 | HG00558.hp2 HG01069.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.2368+390G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253573 | ||||||
| chr3:154253579
|
A | T | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2368+396A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253579 | ||||||
| chr3:154253638
|
A | G | 1 | a0002c0002t0003g0084 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2368+455A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253638 | ||||||
| chr3:154253813
|
T | C | 194 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2368+630T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253813 | ||||||
| chr3:154253951
|
G | A | 4 | a0001c0001t0007g0206a0001c0001t0007g0274a0002c0003t0003g0089others(1): Show | 4 | HG01069.hp1 HG01255.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2368+768G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253951 | ||||||
| chr3:154253976
|
T | C | 187 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2369-744T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253976 | ||||||
| chr3:154253980
|
A | T | 1 | a0002c0002t0052g0082 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2369-740A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154253980 | ||||||
| chr3:154254011
|
G | T | 3 | a0001c0001t0041g0165a0001c0009t0022g0163a0001c0009t0022g0164 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2369-709G>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154254011 | ||||||
| chr3:154254073
|
GC | G | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2369-644delC | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 154254073 | |||||
| chr3:154254210
|
C | T | 1 | a0001c0001t0039g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2369-510C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154254210 | ||||||
| chr3:154254260
|
TG | T | 3 | a0002c0002t0006g0027a0002c0002t0006g0029a0002c0002t0006g0063 | 3 | NA18946.hp2 NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2369-458delG | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 154254260 | |||||
| chr3:154254322
|
T | TG | 3 | a0001c0001t0009g0004a0001c0001t0009g0261a0002c0003t0025g0105 | 4 | HG02280.hp1 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2369-394dupG | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr3 | 154254322 | |||||
| chr3:154254332
|
C | T | 1 | a0002c0003t0005g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2369-388C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154254332 | ||||||
| chr3:154254711
|
T | C | 270 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0150others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2369-9T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154254711 | ||||||
| chr3:154254716
|
T | G | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.2369-4T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 13/14 | chr3 | 154254716 | ||||||
| chr3:154254952
|
T | C | 2 | a0002c0002t0003g0024a0002c0002t0003g0083 | 2 | NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.2473+128T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/14 | chr3 | 154254952 | ||||||
| chr3:154255164
|
C | T | 1 | a0002c0002t0003g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2474-167C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/14 | chr3 | 154255164 | ||||||
| chr3:154255188
|
G | A | 1 | a0001c0001t0035g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2474-143G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/14 | chr3 | 154255188 | ||||||
| chr3:154255204
|
C | A | 5 | a0001c0001t0015g0124a0001c0001t0015g0126a0001c0001t0015g0127others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2474-127C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/14 | chr3 | 154255204 | ||||||
| chr3:154255320
|
C | T | 3 | a0001c0001t0023g0131a0001c0001t0043g0134a0005c0008t0023g0123 | 3 | HG01891.hp2 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2474-11C>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 14/14 | chr3 | 154255320 |