Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 871 | 158 | 36 | 33 | 61 | 11 | 16 | 45 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0002 | 0/0 | 871 | 105 | 23 | 12 | 58 | 3 | 9 | 41 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0003 | 0/0 | 871 | 10 | 2 | 7 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0004 | 0/0 | 871 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0005 | 0/0 | 871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0006 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0007 | 0/0 | 871 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0008 | 0/0 | 871 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0009 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| a0010 | 0/0 | 871 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | MDGES others(866): Show |
chr3 | 154116390 | 154262825 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2613 | 151 | 32 | 31 | 61 | 11 | 15 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0001c0006 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0001c0008 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0001c0009 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0001c0015 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0002c0002 | 0/0 | 2613 | 64 | 5 | 9 | 40 | 3 | 7 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0002c0003 | 0/0 | 2613 | 38 | 16 | 3 | 18 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0002c0007 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0002c0014 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0003c0004 | 0/0 | 2613 | 10 | 2 | 7 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0004c0005 | 0/0 | 2613 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0005c0012 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0005c0013 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0006c0016 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0007c0018 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0008c0017 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0009c0011 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 | ||
| a0010c0010 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | ATGGA others(2608): Show |
chr3 | 154116390 | 154262825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5149 | 45 | 8 | 10 | 21 | 2 | 4 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0002 | 0/0 | 5149 | 43 | 3 | 12 | 20 | 4 | 4 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0004 | 0/0 | 5150 | 26 | 4 | 5 | 13 | 4 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0007 | 0/0 | 5150 | 9 | 1 | 2 | 4 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0009 | 0/0 | 5149 | 3 | 1 | 0 | 0 | 0 | 2 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0011 | 0/0 | 5151 | 4 | 0 | 1 | 2 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0012 | 0/0 | 5147 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5142): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0013 | 0/0 | 5146 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5141): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0014 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0015 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0018 | 0/0 | 5150 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0019 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5147): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0020 | 0/0 | 5149 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0021 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0023 | 0/1 | 5149 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0024 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0025 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5142): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0028 | 0/0 | 5149 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0029 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0030 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0031 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0001c0001t0032 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0001c0006t0014 | 0/0 | 5150 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0001c0008t0012 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5142): Show |
chr3 | 154116390 | 154262825 |
| a0001c0008t0019 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5147): Show |
chr3 | 154116390 | 154262825 |
| a0001c0009t0015 | 0/0 | 5149 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0001c0015t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0003 | 0/0 | 5150 | 34 | 0 | 6 | 23 | 1 | 4 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0005 | 0/0 | 5149 | 6 | 3 | 1 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0006 | 0/0 | 5150 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0008 | 0/0 | 5151 | 7 | 0 | 0 | 5 | 1 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0010 | 0/0 | 5149 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0017 | 0/0 | 5149 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0022 | 0/0 | 5150 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0037 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0040 | 0/0 | 5138 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5133): Show |
chr3 | 154116390 | 154262825 |
| a0002c0002t0041 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0003 | 0/0 | 5150 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0004 | 0/0 | 5150 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0005 | 0/0 | 5149 | 17 | 3 | 1 | 12 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0006 | 0/0 | 5150 | 7 | 1 | 1 | 5 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0010 | 0/0 | 5149 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0016 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0017 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0034 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5141): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0035 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5147): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0036 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0038 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0002c0003t0039 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0002c0007t0016 | 0/0 | 5151 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0002c0014t0010 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0002 | 0/0 | 5149 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0004 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0009 | 0/0 | 5149 | 4 | 0 | 3 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0021 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0026 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5149): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0027 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5148): Show |
chr3 | 154116390 | 154262825 |
| a0003c0004t0033 | 0/0 | 5149 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0004c0005t0001 | 0/0 | 5149 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0005c0012t0008 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5146): Show |
chr3 | 154116390 | 154262825 |
| a0005c0013t0010 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0006c0016t0001 | 0/0 | 5149 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0007c0018t0007 | 0/0 | 5150 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5145): Show |
chr3 | 154116390 | 154262825 |
| a0008c0017t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0009c0011t0005 | 0/0 | 5149 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| a0010c0010t0002 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | GGGCC others(5144): Show |
chr3 | 154116390 | 154262825 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0155 | 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0193 | 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 |
| a0001c0001t0001g0196 | 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 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0243 | 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 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0011g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0012g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0015g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0018g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0019g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0020g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0021g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0023g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0024g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0028g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0029g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0030g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0001t0032g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0006t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0006t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0008t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0008t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0009t0015g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0009t0015g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0001c0015t0002g0142 | 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 | 0 | 0 | 1 | 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 |
| a0002c0002t0003g0027 | 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 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0062 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0002c0002t0003g0072 | 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 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0005g0022 | 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 |
| a0002c0002t0005g0061 | 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 |
| a0002c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0057 | 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 |
| a0002c0002t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0021 | 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 |
| a0002c0002t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0008g0075 | 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 |
| a0002c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0010g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0017g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0022g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0022g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0037g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0040g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0002t0041g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0003t0004g0087 | 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 |
| a0002c0003t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0003t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0003t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0003t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0003t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0016g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0017g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0034g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0035g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0036g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0038g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0003t0039g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0007t0016g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0007t0016g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0002c0014t0010g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0009g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0009g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0009g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0021g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0026g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0027g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0003c0004t0033g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0004c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0005c0012t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0005c0013t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0006c0016t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0007c0018t0007g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0008c0017t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0009c0011t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| a0010c0010t0002g0239 | 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 | g0138 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0170 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0004 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0263 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00323 | hp1 | a0003 | c0004 | t0009 | g0015 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0248 | EUR | FIN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00408 | hp1 | a0002 | c0003 | t0005 | g0114 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00438 | hp1 | a0002 | c0003 | t0005 | g0109 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00544 | hp1 | a0002 | c0003 | t0005 | g0115 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00544 | hp2 | a0001 | c0001 | t0028 | g0201 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00558 | hp1 | a0006 | c0016 | t0001 | g0217 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0069 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00597 | hp1 | a0002 | c0002 | t0006 | g0060 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00609 | hp1 | a0002 | c0003 | t0005 | g0117 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00621 | hp1 | a0002 | c0003 | t0005 | g0111 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | CHS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00741 | hp1 | a0001 | c0001 | t0011 | g0195 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG00741 | hp2 | a0003 | c0004 | t0009 | g0014 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01069 | hp1 | a0002 | c0003 | t0003 | g0090 | 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 | t0002 | g0002 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01071 | hp2 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01081 | hp1 | a0002 | c0002 | t0041 | g0083 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01081 | hp2 | a0003 | c0004 | t0004 | g0012 | 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 | t0021 | g0013 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01106 | hp1 | a0003 | c0004 | t0009 | g0010 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0140 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01167 | hp2 | a0001 | c0009 | t0015 | g0163 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01169 | hp1 | a0001 | c0009 | t0015 | g0162 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01243 | hp1 | a0004 | c0005 | t0001 | g0159 | 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 | g0205 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01255 | hp2 | a0003 | c0004 | t0033 | g0017 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0068 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01258 | hp2 | a0003 | c0004 | t0009 | g0016 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01358 | hp1 | a0003 | c0004 | t0002 | g0008 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01361 | hp2 | a0002 | c0003 | t0005 | g0119 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01433 | hp1 | a0002 | c0003 | t0006 | g0097 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01496 | hp1 | a0007 | c0018 | t0007 | g0007 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0218 | EUR | IBS | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01516 | hp1 | a0008 | c0017 | t0002 | g0169 | 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 | g0224 | 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 | t0005 | g0104 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01884 | hp2 | a0001 | c0006 | t0014 | g0130 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0132 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0080 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0067 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01993 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02055 | hp1 | a0005 | c0012 | t0008 | g0019 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02055 | hp2 | a0001 | c0008 | t0019 | g0124 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02056 | hp1 | a0002 | c0003 | t0005 | g0121 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02071 | hp2 | a0002 | c0002 | t0010 | g0063 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02074 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02132 | hp2 | a0002 | c0003 | t0005 | g0110 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02135 | hp2 | a0002 | c0003 | t0006 | g0112 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02145 | hp1 | a0001 | c0001 | t0031 | g0254 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0128 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02155 | hp2 | a0002 | c0003 | t0005 | g0108 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0058 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02257 | hp2 | a0009 | c0011 | t0005 | g0018 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02258 | hp2 | a0002 | c0003 | t0010 | g0103 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0125 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02523 | hp1 | a0002 | c0002 | t0005 | g0022 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02572 | hp1 | a0001 | c0001 | t0025 | g0126 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0143 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02602 | hp2 | a0010 | c0010 | t0002 | g0239 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02622 | hp2 | a0002 | c0003 | t0004 | g0087 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02630 | hp1 | a0004 | c0005 | t0001 | g0137 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02630 | hp2 | a0002 | c0003 | t0039 | g0100 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0127 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02717 | hp2 | a0001 | c0001 | t0020 | g0134 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02735 | hp1 | a0002 | c0002 | t0017 | g0056 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0133 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02818 | hp1 | a0001 | c0006 | t0014 | g0129 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0275 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02886 | hp2 | a0001 | c0001 | t0029 | g0253 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02922 | hp2 | a0005 | c0013 | t0010 | g0020 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0024 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03041 | hp2 | a0002 | c0002 | t0040 | g0033 | AFR | GWD | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03098 | hp1 | a0001 | c0008 | t0012 | g0123 | 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 | t0016 | g0091 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03195 | hp2 | a0003 | c0004 | t0027 | g0009 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03209 | hp1 | a0002 | c0003 | t0003 | g0099 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03209 | hp2 | a0002 | c0003 | t0017 | g0105 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03225 | hp1 | a0002 | c0003 | t0004 | g0086 | 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 | t0009 | g0145 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03239 | hp2 | a0001 | c0001 | t0024 | g0152 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03453 | hp1 | a0002 | c0003 | t0034 | g0095 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0136 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0051 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0221 | 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 | g0161 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03516 | hp1 | a0002 | c0007 | t0016 | g0092 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03579 | hp1 | a0002 | c0003 | t0038 | g0098 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03579 | hp2 | a0001 | c0001 | t0032 | g0135 | AFR | MSL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03710 | hp2 | a0001 | c0001 | t0020 | g0209 | SAS | PJL | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0186 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03834 | hp2 | a0002 | c0014 | t0010 | g0040 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03927 | hp1 | a0002 | c0003 | t0005 | g0113 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0237 | SAS | BEB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG04115 | hp1 | a0002 | c0002 | t0008 | g0021 | SAS | STU | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG04115 | hp2 | a0001 | c0015 | t0002 | g0142 | SAS | STU | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18522 | hp1 | a0002 | c0003 | t0010 | g0106 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0048 | EAS | CHB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18906 | hp1 | a0002 | c0003 | t0006 | g0089 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0168 | 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 | g0258 | 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 | g0065 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0272 | 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 | g0107 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18948 | hp1 | a0002 | c0003 | t0006 | g0101 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0270 | 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 | g0277 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18954 | hp1 | a0002 | c0002 | t0006 | g0049 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18962 | hp1 | a0002 | c0002 | t0003 | g0055 | 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 | g0193 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18964 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18967 | hp2 | a0002 | c0002 | t0006 | g0057 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18969 | hp2 | a0002 | c0003 | t0005 | g0120 | 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 | g0074 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18978 | hp1 | a0002 | c0003 | t0006 | g0102 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18979 | hp1 | a0002 | c0002 | t0010 | g0046 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18983 | hp2 | a0002 | c0002 | t0006 | g0064 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18984 | hp2 | a0002 | c0002 | t0017 | g0047 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18985 | hp1 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0199 | 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 | g0250 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18989 | hp2 | a0002 | c0002 | t0005 | g0061 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0210 | 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 | g0188 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA18999 | hp2 | a0002 | c0002 | t0008 | g0075 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19001 | hp1 | a0002 | c0002 | t0008 | g0082 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19006 | hp2 | a0001 | c0001 | t0011 | g0165 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19007 | hp2 | a0002 | c0002 | t0006 | g0059 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0276 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19030 | hp2 | a0002 | c0003 | t0035 | g0096 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19043 | hp1 | a0003 | c0004 | t0026 | g0011 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19043 | hp2 | a0002 | c0003 | t0036 | g0094 | AFR | LWK | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19054 | hp2 | a0002 | c0003 | t0006 | g0118 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19056 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0261 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0178 | 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 | g0238 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19082 | hp2 | a0002 | c0002 | t0008 | g0081 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19084 | hp1 | a0002 | c0003 | t0006 | g0116 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19086 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19090 | hp1 | a0002 | c0003 | t0005 | g0122 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19240 | hp1 | a0001 | c0001 | t0021 | g0274 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | YRI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20129 | hp1 | a0002 | c0002 | t0037 | g0041 | AFR | ASW | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0160 | AFR | ASW | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20805 | hp1 | a0002 | c0002 | t0022 | g0079 | EUR | TSI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20905 | hp1 | a0002 | c0002 | t0010 | g0035 | SAS | GIH | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0053 | SAS | GIH | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG01123 | hp2 | a0002 | c0002 | t0022 | g0078 | AMR | CLM | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02109 | hp1 | a0001 | c0001 | t0030 | g0204 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG02109 | hp2 | a0002 | c0003 | t0005 | g0088 | AFR | ACB | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0164 | AFR | USA | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0139 | AFR | USA | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| NA21309 | hp1 | a0002 | c0003 | t0016 | g0093 | 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 | a0001 | c0001 | t0023 | g0265 | REF | REF | ARHGEF26_chr3_154116390_154262825 | ARHGEF26 | chr3 | 154116390 | 154262825 |
| view | 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 | a0010 | 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 | 8 | a0001 a0002 a0004 others(5): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001 | 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 | a0009 | 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 | a0001 a0004 a0006 others(2): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): 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 | 8 | a0001 a0002 a0004 others(5): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0005 a0009 |
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 | a0002 a0005 a0007 others(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 | a0006 | 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 |
| view | 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 | a0002c0002 a0002c0014 a0005c0012 others(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 | a0005c0012 | 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 |
| view | 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 | 26 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0006 others(23): 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 | a0002c0003t0016 a0002c0003t0034 a0002c0003t0035 others(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 | a0002c0002t0022 | 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 | a0002c0002t0041 | 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 | a0002c0002t0040 | 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 | 11 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0024 others(8): Show |
57 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(54): 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 | a0001c0001t0012 a0001c0008t0012 |
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 | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | a0001c0001t0001 a0001c0001t0019 a0001c0001t0029 others(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 | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(61): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0015 a0001c0009t0015 |
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 | a0001c0001t0029 | 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 | 24 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0019 others(21): 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 | a0001c0001t0014 a0001c0006t0014 a0002c0003t0039 |
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 | a0001c0001t0024 | 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 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(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 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0030 others(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 | a0001c0001t0028 | 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 | a0002c0002t0040 | 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 | a0001c0001t0001 | 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 | a0001c0001t0002 a0002c0003t0010 a0005c0013t0010 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(10): Show |
47 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(44): 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 | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(49): 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 | 24 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0019 others(21): 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 | a0001c0001t0025 | 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 | a0001c0001t0029 | 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 | a0001c0001t0019 a0001c0001t0032 a0001c0008t0019 |
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 | a0003c0004t0026 a0003c0004t0027 |
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 | a0002c0002t0037 | 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 | a0001c0001t0012 a0001c0008t0012 |
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 | a0001c0001t0013 a0001c0001t0025 a0002c0003t0034 |
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 | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0014 a0001c0001t0031 a0001c0006t0014 others(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 | a0001c0001t0015 a0001c0009t0015 |
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 |
| view | 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 | 145 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): 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 | a0002c0003t0005g0136 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0004c0005t0001g0137 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0003t0003g0099 a0002c0003t0003g0107 a0002c0003t0005g0001 others(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 | a0001c0001t0004g0277 | 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 | a0001c0001t0007g0273 a0001c0001t0012g0275 a0001c0001t0012g0276 others(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 | a0002c0003t0003g0099 a0002c0003t0006g0097 a0002c0003t0038g0098 others(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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0004g0277 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | 273 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0002c0003t0003g0090 a0002c0003t0003g0099 a0002c0003t0003g0107 others(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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0005c0012t0008g0019 a0005c0013t0010g0020 a0009c0011t0005g0018 |
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 | a0001c0001t0004g0138 a0001c0001t0004g0140 a0001c0001t0009g0139 |
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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0266 others(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 | a0002c0002t0003g0024 a0002c0002t0003g0025 a0002c0002t0003g0026 others(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 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0038 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0131 a0001c0001t0014g0133 a0001c0001t0019g0132 others(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 | a0002c0002t0003g0085 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1123+453A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 3/14 | chr3 | 154124902 | |||||||
| chr3:154124978 | CA | C | 246 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0154 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0008t0019g0124 | 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 | a0001c0001t0004g0264 | 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 | a0002c0002t0003g0023 | 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 | a0002c0003t0003g0099 a0002c0003t0039g0100 |
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 | a0001c0001t0032g0135 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0001g0147 a0001c0001t0004g0148 a0001c0001t0004g0149 |
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 | a0001c0001t0004g0150 | 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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | 148 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(145): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0002t0003g0084 | 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 | a0001c0001t0004g0150 | 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 | a0002c0002t0041g0083 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0002g0263 | 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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0001g0262 | 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 | a0001c0001t0004g0006 a0001c0001t0004g0260 a0001c0001t0011g0261 |
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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | 154 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(151): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): 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 | a0001c0001t0002g0266 a0002c0002t0003g0023 a0002c0002t0003g0024 others(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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0002c0002t0005g0022 | 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 | a0002c0003t0010g0103 | 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 | 152 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(149): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0259 |
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 | 143 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0002g0146 | 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 | 143 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): 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 | a0002c0003t0006g0102 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0002g0153 a0001c0001t0024g0152 |
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 | a0002c0002t0008g0021 | 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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0003t0005g0122 a0002c0003t0006g0101 |
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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 139 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): 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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0002t0003g0080 a0002c0002t0008g0081 a0002c0002t0008g0082 others(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 | a0002c0003t0005g0121 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0003t0003g0099 a0002c0003t0005g0104 a0002c0003t0005g0136 others(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 | a0001c0001t0007g0143 a0001c0015t0002g0142 |
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 | a0002c0003t0010g0106 | 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0004g0144 | 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 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
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 | a0002c0003t0005g0088 | 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 | a0002c0003t0003g0107 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0032g0135 | 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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0002c0002t0022g0078 a0002c0002t0022g0079 |
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 | a0002c0003t0006g0089 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0004g0246 | 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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0002g0245 | 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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0001c0001t0002g0266 a0001c0001t0002g0270 a0001c0001t0002g0271 others(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 | a0001c0001t0020g0134 | 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 | a0002c0003t0005g0119 | 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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | 156 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(153): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0001g0244 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0012g0276 | 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 | a0003c0004t0009g0015 | 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 | a0002c0002t0010g0035 | 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 | a0005c0013t0010g0020 | 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 | a0002c0003t0017g0105 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0020g0134 | 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 | a0001c0001t0004g0246 | 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 |
34 | a0001c0001t0001g0232 a0001c0001t0001g0244 a0001c0001t0002g0141 others(31): Show |
35 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(32): 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 | a0001c0001t0004g0144 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0002g0223 a0001c0001t0002g0243 a0003c0004t0009g0014 others(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 | a0001c0006t0014g0129 a0002c0002t0003g0023 a0002c0002t0003g0024 others(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 | 165 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1269+6551G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154136270 | |||||||
| chr3:154136279 | G | C | 44 | a0001c0001t0001g0232 a0001c0001t0001g0244 a0001c0001t0002g0002 others(41): Show |
46 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(43): 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 |
106 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(103): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 154 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(151): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): 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 | a0001c0001t0011g0165 | 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 | a0001c0001t0002g0242 a0001c0001t0002g0269 |
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 | a0002c0002t0003g0027 a0002c0002t0003g0069 a0002c0002t0003g0070 others(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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0001t0004g0006 a0001c0001t0004g0260 a0001c0001t0011g0261 |
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 | a0001c0001t0001g0166 | 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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0002g0224 | 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | a0001c0001t0002g0153 a0001c0001t0024g0152 |
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 | a0001c0001t0002g0225 | 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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0001t0002g0247 | 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 | a0002c0002t0003g0027 a0002c0002t0003g0066 a0002c0002t0003g0069 others(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 | 51 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0172 others(48): 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 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0002g0227 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | a0001c0001t0001g0203 a0001c0001t0002g0202 |
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 | a0001c0001t0002g0259 | 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 | 144 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(141): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 65 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0155 others(62): 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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | 153 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(150): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): 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 | a0001c0001t0001g0154 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0005c0012t0008g0019 | 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 | a0002c0003t0003g0090 a0002c0003t0003g0107 a0002c0003t0004g0086 others(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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0003g0026 a0002c0002t0003g0065 a0002c0002t0008g0032 |
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 | a0001c0001t0001g0203 a0001c0001t0002g0202 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0002t0003g0023 others(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 | a0001c0015t0002g0142 | 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 | 131 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(128): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0002t0003g0023 others(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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0004g0170 a0001c0001t0004g0218 a0001c0001t0004g0248 others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0011g0261 | 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 | a0002c0002t0003g0023 a0002c0002t0003g0037 a0002c0002t0003g0038 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0007g0171 | 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 | a0002c0002t0006g0064 | 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 | a0001c0001t0001g0172 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0028g0201 | 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 | a0001c0001t0002g0141 a0001c0001t0007g0143 a0001c0015t0002g0142 |
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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0002t0003g0023 others(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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0002c0002t0003g0069 | 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0002t0003g0023 others(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 | a0001c0001t0001g0244 a0001c0001t0002g0141 a0001c0001t0002g0153 others(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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0001g0197 | 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 | a0002c0002t0003g0077 a0002c0002t0008g0082 |
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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1270-3673A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 4/14 | chr3 | 154145716 | |||||||
| chr3:154145909 | A | T | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0002t0003g0023 others(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 | a0002c0002t0003g0067 | 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 | a0002c0003t0003g0107 a0002c0003t0005g0001 a0002c0003t0005g0108 others(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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0002c0014t0010g0040 | 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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0244 a0001c0001t0009g0237 |
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 | a0002c0002t0003g0023 a0002c0002t0003g0024 a0002c0002t0003g0025 others(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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0002c0003t0038g0098 | 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | 273 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0001c0001t0007g0161 | 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 | a0002c0003t0005g0088 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0015t0002g0142 | 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 | a0001c0001t0002g0245 | 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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0252 | 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 | a0002c0002t0040g0033 | 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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0030g0204 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0002c0002t0003g0037 a0002c0002t0005g0034 a0002c0002t0005g0042 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0002g0223 a0001c0001t0002g0225 a0001c0001t0002g0236 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0001c0001t0004g0277 | 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 | 251 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): 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 | a0001c0001t0004g0277 | 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 | 149 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0002c0002t0003g0039 a0002c0002t0003g0058 a0002c0002t0003g0062 others(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 | a0001c0001t0030g0204 | 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 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0002c0003t0006g0118 | 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 | a0001c0001t0002g0263 | 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 | a0001c0001t0004g0260 | 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 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0001c0001t0002g0202 | 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 | a0002c0002t0003g0066 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0001c0001t0001g0206 a0001c0001t0004g0207 |
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 | a0001c0001t0001g0203 a0001c0001t0002g0202 a0002c0003t0010g0106 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1327-154G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 5/14 | chr3 | 154152618 | |||||||
| chr3:154152722 | G | A | 149 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0001c0001t0001g0194 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0193 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0156 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0002g0269 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0004g0192 | 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 | a0002c0003t0005g0001 a0002c0003t0005g0108 a0002c0003t0005g0109 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 230 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1487+1624A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154154556 | |||||||
| chr3:154154573 | TATAG | T | 142 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(139): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): 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 | a0002c0003t0003g0090 a0002c0003t0003g0107 a0002c0003t0004g0086 others(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 | 230 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0004c0005t0001g0160 | 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 | a0001c0001t0001g0131 a0001c0001t0014g0133 a0001c0001t0019g0132 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0002c0003t0010g0103 | 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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0001t0014g0133 | 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 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
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 | 149 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0001c0001t0007g0219 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0002g0235 | 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 | a0002c0003t0010g0103 | 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 | a0001c0001t0002g0266 a0001c0001t0002g0270 a0001c0001t0002g0271 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0004g0167 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0001g0194 a0001c0001t0004g0192 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0003t0005g0117 | 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 | 63 | a0001c0001t0001g0147 a0001c0001t0001g0203 a0001c0001t0001g0206 others(60): Show |
65 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(62): 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0030g0204 | 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 | a0002c0003t0003g0090 a0002c0003t0003g0107 a0002c0003t0004g0086 others(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 | a0002c0003t0003g0090 a0002c0003t0003g0107 a0002c0003t0004g0086 others(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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0003t0003g0090 others(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 | 230 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0003t0003g0090 others(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 | a0002c0003t0005g0117 | 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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0001c0001t0001g0172 | 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 | 1 | a0001c0001t0002g0002 | 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 | a0007c0018t0007g0007 | 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 | a0002c0003t0003g0090 a0002c0003t0003g0107 a0002c0003t0004g0086 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0002c0003t0005g0121 a0002c0003t0006g0116 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0038g0098 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0002g0227 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0010g0106 | 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 | a0001c0001t0032g0135 | 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 | 149 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0001c0001t0002g0230 | 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0003t0003g0090 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0002g0234 | 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 | a0001c0001t0004g0277 | 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 | a0008c0017t0002g0169 | 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 | a0001c0001t0012g0276 | 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 | a0001c0001t0002g0258 | 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 | a0001c0001t0009g0139 | 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 | a0002c0003t0005g0115 a0002c0003t0005g0120 a0002c0003t0005g0122 others(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 | a0002c0003t0005g0001 a0002c0003t0005g0104 a0002c0003t0005g0108 others(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 | a0001c0006t0014g0129 a0001c0006t0014g0130 a0002c0003t0004g0086 others(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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0002g0247 a0001c0001t0004g0150 a0001c0001t0007g0205 others(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 | 39 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0206 others(36): 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 | 87 | a0001c0001t0001g0151 a0001c0001t0001g0172 a0001c0001t0001g0173 others(84): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): 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 | a0002c0002t0010g0035 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0002c0002t0010g0046 a0002c0003t0016g0093 a0002c0003t0034g0095 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0002c0003t0003g0107 a0002c0003t0005g0115 a0002c0003t0005g0117 others(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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0001t0002g0263 | 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 |
263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0002t0005g0061 | 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 | a0002c0002t0005g0061 | 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 | a0001c0001t0018g0004 | 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 | a0005c0012t0008g0019 | 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 | a0001c0001t0001g0131 a0001c0001t0014g0133 a0001c0001t0019g0132 |
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 | |||||||
| chr3:154162772 | C | T | 2 | a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0001c0001t0001g0175 a0001c0001t0002g0223 a0001c0001t0002g0236 |
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 | a0001c0001t0002g0189 | 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 147 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0002c0002t0003g0080 | 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 | a0001c0001t0013g0127 | 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 | a0002c0003t0005g0122 a0002c0003t0006g0101 |
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 | a0001c0001t0004g0170 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0012g0275 | 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 | a0002c0002t0005g0034 a0002c0002t0005g0042 a0002c0002t0005g0043 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0011g0165 | 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 | a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0011g0261 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0011g0261 others(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 | a0001c0001t0004g0208 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0004g0087 | 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 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0011g0261 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 a0001c0008t0019g0124 |
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 | a0001c0001t0007g0171 | 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 | a0001c0001t0007g0273 a0001c0001t0012g0275 a0001c0001t0012g0276 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0005g0136 | 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 | 176 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(173): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): 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 | a0002c0014t0010g0040 | 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 | a0002c0002t0003g0026 a0002c0002t0003g0065 a0002c0002t0008g0032 |
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 | a0002c0003t0005g0121 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0188 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0001c0001t0002g0225 a0001c0001t0002g0231 a0001c0001t0002g0245 others(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 | a0001c0008t0019g0124 | 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 | a0002c0002t0040g0033 a0002c0003t0010g0106 a0002c0007t0016g0091 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0007g0219 | 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 | 171 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): 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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | a0001c0001t0001g0252 | 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 | a0002c0002t0003g0026 | 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 | a0002c0003t0010g0106 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1487+14285A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154167217 | |||||||
| chr3:154167410 | G | C | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0002t0040g0033 | 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 | a0002c0002t0017g0056 | 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 | 132 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(129): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0009g0139 | 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 | a0002c0002t0010g0063 | 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 | 129 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(126): Show |
129 | HG00280.hp1 HG00558.hp2 HG00597.hp1 others(126): 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 | a0001c0001t0001g0175 a0001c0001t0001g0232 a0001c0001t0004g0144 |
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 | a0002c0003t0006g0116 | 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 | a0008c0017t0002g0169 | 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 | a0001c0001t0001g0203 | 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 | 132 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(129): 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 | a0002c0003t0039g0100 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 a0001c0001t0014g0133 others(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 | a0001c0001t0001g0131 a0001c0001t0019g0132 a0001c0001t0032g0135 others(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 | a0002c0003t0010g0106 | 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 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0002c0002t0003g0055 | 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 | a0001c0001t0002g0146 a0001c0001t0009g0145 a0003c0004t0009g0014 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0013g0125 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 131 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(128): 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 | 131 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(128): 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 | a0002c0002t0022g0078 a0002c0002t0022g0079 |
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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0004g0212 | 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 | a0002c0002t0006g0029 a0002c0002t0006g0057 a0002c0002t0006g0064 |
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 | 133 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(130): 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 | 131 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(128): 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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0002c0002t0003g0023 others(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 | a0001c0001t0002g0146 a0001c0001t0009g0145 a0003c0004t0002g0008 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0002t0006g0029 a0002c0002t0006g0057 a0002c0002t0006g0064 |
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 | 133 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(130): 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 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0002g0241 | 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 | a0002c0003t0010g0106 | 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 | a0001c0001t0004g0006 a0001c0001t0004g0260 a0001c0001t0011g0261 |
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 | a0001c0001t0004g0211 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0175 a0001c0001t0001g0187 others(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 | a0001c0001t0004g0149 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1488-14292A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154173393 | |||||||
| chr3:154173428 | A | G | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): 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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0007t0016g0091 others(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 | a0001c0001t0002g0223 | 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 | a0002c0003t0010g0106 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0002t0037g0041 | 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 | a0001c0001t0001g0203 | 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 | a0004c0005t0001g0137 a0004c0005t0001g0159 a0004c0005t0001g0160 |
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 | 129 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(126): 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 | 129 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(126): 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0002c0003t0005g0119 | 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 | a0001c0001t0001g0131 a0001c0001t0019g0132 a0001c0008t0019g0124 |
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 | a0001c0001t0007g0273 a0001c0001t0012g0275 a0001c0001t0012g0276 others(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 | a0001c0001t0007g0177 | 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 | a0001c0001t0029g0253 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0029g0253 | 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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | a0005c0012t0008g0019 | 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 | 66 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0155 others(63): 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0001c0001t0001g0196 | 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 | 204 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(201): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0002t0003g0026 a0002c0002t0005g0061 a0002c0003t0003g0090 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0194 a0001c0001t0004g0192 |
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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0007t0016g0091 others(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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0002c0002t0003g0026 a0002c0002t0005g0061 a0002c0003t0003g0090 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0003t0005g0114 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0002c0003t0005g0119 | 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 | a0003c0004t0002g0008 | 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 | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0002g0141 a0001c0015t0002g0142 a0002c0002t0010g0035 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 128 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(125): 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 | a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | 128 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(125): 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 | a0002c0002t0010g0035 a0002c0002t0010g0063 |
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 | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0003c0004t0026g0011 | 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 | a0002c0002t0003g0027 a0002c0002t0003g0069 a0002c0002t0003g0070 others(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 | a0001c0001t0007g0161 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0008t0012g0123 | 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 | a0001c0001t0020g0134 | 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 | a0001c0001t0002g0226 | 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 | a0001c0001t0002g0227 | 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 | a0001c0001t0002g0225 a0001c0001t0002g0231 a0001c0001t0002g0245 others(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 |
34 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(31): Show |
34 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(31): 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 | a0001c0001t0002g0241 a0002c0002t0010g0035 |
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 | a0001c0001t0001g0151 | 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 |
120 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0154 others(117): 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0018g0004 | 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 | a0001c0001t0004g0140 a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0001c0001t0011g0195 | 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 | a0002c0002t0040g0033 a0002c0003t0016g0093 a0002c0003t0034g0095 others(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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0030g0204 | 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 | a0001c0001t0001g0244 a0001c0001t0009g0237 |
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 | 202 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(199): 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 | 261 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0002c0002t0003g0026 a0002c0003t0005g0121 a0002c0003t0006g0116 |
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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0003t0005g0121 | 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 | a0002c0002t0003g0053 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0004g0277 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0249 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0012g0275 | 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 | 54 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0168 others(51): 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0002c0002t0022g0078 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0011g0186 | 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 | a0002c0003t0010g0103 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0037g0041 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0002c0002t0003g0023 | 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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | a0001c0001t0004g0256 a0001c0001t0011g0165 |
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 | 275 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 |
42 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): 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 | a0001c0001t0031g0254 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | a0002c0002t0003g0037 a0002c0002t0008g0036 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0002t0003g0052 | 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 | a0001c0001t0007g0205 a0002c0003t0003g0099 |
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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 others(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 | 1 | a0001c0001t0002g0002 | 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 | 60 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(57): Show |
61 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(58): 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 | a0001c0001t0015g0164 | 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 | 261 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0168 a0001c0001t0001g0188 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0168 | 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 | 96 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(93): 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 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
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 | 60 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(57): Show |
61 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(58): 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 | a0002c0002t0003g0080 | 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 | a0002c0002t0003g0039 a0002c0002t0003g0058 a0002c0002t0003g0085 |
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 | a0002c0002t0005g0042 a0002c0002t0005g0043 a0002c0003t0039g0100 |
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 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0012g0276 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0249 a0001c0001t0002g0202 others(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 |
89 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(86): 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 |
48 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0191 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(46): 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 | a0001c0001t0001g0157 a0001c0001t0001g0198 a0001c0001t0001g0244 others(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 | a0001c0001t0002g0141 a0001c0001t0002g0234 a0001c0001t0009g0237 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0002c0003t0035g0096 | 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 | a0001c0001t0001g0131 a0001c0001t0019g0132 a0001c0001t0032g0135 others(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 | a0001c0001t0004g0255 a0001c0001t0004g0264 a0002c0003t0003g0090 others(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 | 60 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(57): Show |
61 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1488-1412G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186273 | |||||||
| chr3:154186370 | TATA | T | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | 60 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(57): Show |
61 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1488-1126G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 6/14 | chr3 | 154186559 | |||||||
| chr3:154186886 | C | CT | 76 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(73): 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 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | 26 | a0001c0001t0002g0190 a0001c0001t0002g0202 a0001c0001t0002g0215 others(23): Show |
27 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(24): 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 | a0001c0001t0002g0214 a0001c0001t0002g0225 a0001c0001t0002g0235 others(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 | a0002c0003t0016g0093 a0002c0003t0036g0094 |
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 | a0002c0003t0034g0095 | 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 | a0002c0003t0035g0096 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0219 | 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 | a0002c0003t0010g0103 | 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 | 139 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0004g0006 a0001c0001t0004g0260 |
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 | a0001c0001t0015g0164 | 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 | a0001c0001t0001g0173 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1640+158A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154187995 | |||||||
| chr3:154188199 | T | A | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0007g0273 a0001c0001t0012g0275 a0001c0001t0012g0276 others(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 | a0002c0002t0010g0035 a0002c0002t0010g0063 |
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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | 49 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(46): Show |
50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0002t0040g0033 | 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 | a0002c0003t0038g0098 | 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 | 127 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(124): 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 | a0001c0001t0011g0261 | 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 | 132 | a0001c0001t0001g0244 a0001c0001t0001g0252 a0001c0001t0001g0267 others(129): Show |
133 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(130): 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 | a0001c0001t0001g0203 a0001c0001t0002g0214 a0001c0001t0002g0235 others(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 | 27 | a0001c0001t0001g0147 a0001c0001t0002g0210 a0001c0001t0004g0003 others(24): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 61 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0155 others(58): 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 | a0008c0017t0002g0169 | 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 | a0002c0002t0005g0034 a0002c0002t0005g0042 a0002c0002t0005g0043 others(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 | 101 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(98): 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 | a0001c0001t0002g0225 | 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 | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1641-1260T>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 7/14 | chr3 | 154190029 | |||||||
| chr3:154190030 | T | A | 48 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(45): Show |
48 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(45): 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 | a0001c0001t0004g0170 a0001c0001t0004g0218 a0001c0001t0004g0248 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0232 | 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 | a0002c0002t0022g0078 a0002c0002t0022g0079 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0181 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0008t0012g0123 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0268 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1770+739T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 8/14 | chr3 | 154192157 | |||||||
| chr3:154192199 | T | C | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0008c0017t0002g0169 | 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 | a0001c0001t0011g0195 | 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 | 105 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(102): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0003t0006g0101 | 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 | 43 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0168 others(40): 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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | a0001c0001t0004g0218 | 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 | a0001c0001t0004g0218 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0002g0190 a0001c0001t0002g0229 |
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 | 49 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(46): Show |
50 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(47): 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 | a0001c0001t0020g0134 | 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 | a0001c0008t0012g0123 | 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 | a0001c0001t0001g0181 | 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 | a0002c0002t0003g0025 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0029g0253 | 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 | a0002c0002t0005g0034 a0002c0002t0005g0042 a0002c0002t0005g0043 others(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 | a0002c0002t0003g0026 a0002c0002t0005g0061 a0002c0003t0004g0086 others(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 | a0001c0001t0011g0261 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0006c0016t0001g0217 | 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 | a0008c0017t0002g0169 | 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 | a0002c0002t0003g0024 a0002c0002t0003g0051 |
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 | a0001c0001t0020g0134 | 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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | 259 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0029g0253 | 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 | a0002c0002t0003g0066 | 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 | a0002c0002t0003g0027 | 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 | a0001c0001t0011g0195 | 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 | 205 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(202): 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 | a0001c0001t0029g0253 a0002c0002t0040g0033 a0002c0003t0016g0093 others(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 | a0001c0001t0013g0127 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0029g0253 | 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 | a0002c0002t0003g0026 | 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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0002c0002t0017g0056 | 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 | a0002c0002t0003g0026 a0002c0002t0005g0061 a0002c0003t0004g0086 others(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 | 1 | a0001c0001t0002g0002 | 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 | 103 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0154 others(100): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0040g0033 a0002c0003t0016g0093 a0002c0003t0034g0095 others(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 | a0001c0001t0029g0253 | 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 | a0001c0001t0029g0253 | 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 | 264 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0030g0204 a0005c0013t0010g0020 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0003g0062 a0007c0018t0007g0007 |
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 | 2 | a0001c0001t0002g0002 a0001c0001t0002g0189 |
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 | a0002c0002t0017g0056 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0001g0244 a0001c0001t0002g0141 others(44): Show |
47 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(44): 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 | a0002c0002t0017g0056 a0002c0014t0010g0040 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0003c0004t0002g0008 a0003c0004t0004g0012 a0003c0004t0009g0010 |
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 | a0002c0003t0006g0097 | 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 | a0001c0001t0002g0235 | 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 | a0001c0001t0002g0231 | 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 | a0001c0001t0004g0170 | 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 | 47 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(44): Show |
48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | 47 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(44): Show |
48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0012g0276 a0001c0001t0021g0274 |
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 | a0001c0001t0029g0253 | 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 | a0002c0014t0010g0040 | 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 | 29 | a0001c0001t0001g0147 a0001c0001t0002g0210 a0001c0001t0004g0003 others(26): 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 | a0002c0003t0005g0111 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0232 | 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 | a0002c0003t0035g0096 | 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 | a0002c0002t0005g0042 a0002c0002t0005g0043 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0002t0006g0029 a0002c0002t0006g0057 a0002c0002t0006g0064 |
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 | a0001c0001t0028g0201 | 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 | a0001c0001t0014g0133 a0001c0001t0031g0254 a0001c0006t0014g0129 others(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 | a0001c0001t0029g0253 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0002g0263 | 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 | a0002c0003t0005g0117 | 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 | a0002c0003t0035g0096 | 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 | a0001c0001t0002g0153 a0001c0001t0004g0277 a0001c0001t0024g0152 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0021g0274 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0205 | 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 | a0002c0003t0005g0104 a0002c0003t0005g0136 a0002c0003t0006g0097 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0002c0002t0003g0026 a0002c0002t0005g0061 a0002c0003t0004g0086 others(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 | a0002c0003t0005g0109 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0002c0002t0040g0033 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0004g0255 | 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 | a0001c0001t0007g0171 a0001c0001t0007g0174 a0002c0002t0003g0025 others(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 | a0002c0002t0010g0035 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0002g0190 a0001c0001t0002g0270 a0001c0001t0020g0134 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 47 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(44): Show |
48 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(45): 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 | a0002c0002t0017g0056 a0002c0014t0010g0040 |
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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0013g0125 | 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 | 48 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0166 others(45): 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | a0001c0001t0002g0241 | 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 | 206 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(203): 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 | 50 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(47): Show |
50 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(47): 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 | 260 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0002t0003g0053 a0002c0002t0008g0021 |
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 | a0001c0001t0013g0128 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0005c0012t0008g0019 | 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 | 46 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(43): Show |
46 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(43): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0002g0245 | 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 | a0002c0002t0010g0035 | 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 | 207 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(204): 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 | a0002c0002t0003g0080 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0176 | 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 | a0002c0002t0003g0053 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0003t0005g0104 a0002c0003t0005g0136 a0002c0003t0006g0097 others(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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0021g0274 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0002c0002t0003g0050 | 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 | 42 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(39): Show |
42 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(39): 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 | a0002c0002t0003g0066 | 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 | a0002c0003t0038g0098 | 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 | a0001c0001t0001g0179 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0001c0001t0001g0185 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0151 | 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 | a0002c0003t0016g0093 a0002c0003t0034g0095 a0002c0003t0035g0096 others(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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0029g0253 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0244 a0001c0001t0002g0226 others(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 | a0001c0008t0012g0123 a0002c0002t0003g0085 a0002c0002t0005g0028 others(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 | 23 | a0001c0001t0001g0131 a0001c0001t0001g0158 a0001c0001t0001g0267 others(20): 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 | 130 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(127): 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0232 | 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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0185 a0001c0001t0001g0197 others(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 | a0002c0002t0005g0042 a0002c0002t0005g0043 |
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 | a0001c0006t0014g0129 | 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 | 191 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(188): 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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0002c0003t0005g0114 | 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 | a0001c0001t0007g0205 a0002c0003t0003g0099 a0005c0012t0008g0019 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0168 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0259 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0004g0192 | 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 | a0001c0001t0015g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1846-7092A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154210777 | |||||||
| chr3:154210921 | C | A | 1 | a0001c0001t0001g0252 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0001g0200 a0002c0002t0005g0061 a0002c0003t0005g0001 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0205 a0001c0001t0014g0133 a0001c0001t0031g0254 others(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 | a0001c0001t0001g0200 a0001c0001t0001g0252 a0001c0001t0007g0143 others(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 | 100 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(97): 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 | 47 | a0001c0001t0001g0203 a0001c0001t0002g0005 a0001c0001t0002g0153 others(44): Show |
49 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0028g0201 | 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 | 262 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): 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 | a0001c0001t0007g0171 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0004c0005t0001g0160 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0002g0236 | 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 | 253 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): 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 | a0001c0001t0002g0224 a0001c0001t0002g0226 a0001c0001t0002g0227 others(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 | a0001c0001t0001g0194 a0001c0001t0004g0192 |
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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0030g0204 | 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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 210 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(207): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 a0002c0003t0010g0106 |
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 | 183 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(180): 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0020g0134 | 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 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0019g0132 others(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 | a0001c0001t0002g0223 a0001c0001t0013g0125 a0001c0001t0013g0127 others(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 | 99 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0166 others(96): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): 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 | a0001c0001t0002g0153 a0001c0001t0002g0247 a0001c0001t0024g0152 others(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 | a0002c0003t0003g0107 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0002g0223 a0001c0001t0002g0236 a0002c0003t0016g0093 others(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 |
33 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(30): Show |
33 | HG00609.hp2 HG00738.hp2 HG01109.hp1 others(30): 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 | a0001c0001t0002g0263 a0001c0001t0018g0004 |
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 | a0001c0001t0002g0214 a0001c0001t0002g0231 a0001c0001t0002g0233 |
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 | a0001c0015t0002g0142 | 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 | 204 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(201): 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 | a0001c0001t0015g0164 a0001c0001t0020g0134 a0001c0001t0029g0253 others(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 | a0001c0001t0020g0209 | 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 | a0001c0001t0020g0209 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1846-4516A>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154213353 | |||||||
| chr3:154213455 | G | GA | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0004g0148 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0151 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0002t0003g0039 a0002c0002t0003g0058 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0002c0002t0003g0027 a0002c0002t0003g0066 a0002c0002t0003g0069 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0004g0167 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 37 | a0001c0001t0001g0147 a0001c0001t0002g0210 a0001c0001t0004g0003 others(34): 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 | a0002c0002t0003g0068 | 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 | a0001c0001t0029g0253 | 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 | a0002c0003t0005g0136 | 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 | a0001c0001t0002g0234 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0262 | 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 | a0001c0001t0007g0273 a0002c0002t0005g0028 |
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 | a0001c0001t0029g0253 | 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 | a0001c0001t0001g0176 a0002c0003t0010g0106 |
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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0001g0166 a0001c0001t0004g0003 a0001c0015t0002g0142 others(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 | 257 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1846-1377A>T | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216492 | |||||||
| chr3:154216494 | T | A | 249 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): 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 | a0001c0001t0029g0253 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0177 others(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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0001t0001g0267 a0001c0001t0002g0005 a0001c0001t0002g0234 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0220 a0001c0001t0001g0221 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0270 a0001c0001t0002g0271 others(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 | 121 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(118): 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 | 68 | a0001c0001t0001g0203 a0001c0001t0001g0252 a0001c0001t0001g0267 others(65): Show |
69 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1846-1360delA | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216508 | |||||||
| chr3:154216509 | A | T | 6 | a0001c0001t0020g0134 a0001c0001t0029g0253 a0001c0008t0012g0123 others(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 | a0002c0003t0035g0096 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0262 a0001c0001t0004g0150 a0001c0001t0012g0275 others(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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | a0002c0002t0022g0079 | 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 | a0001c0001t0001g0252 a0001c0001t0015g0164 a0001c0009t0015g0162 others(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 | a0002c0002t0022g0079 | 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 | a0001c0001t0002g0245 a0002c0003t0005g0113 |
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 | 263 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1846-1183T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 9/14 | chr3 | 154216686 | |||||||
| chr3:154216778 | C | T | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0002g0257 | 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 | 273 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0002c0003t0006g0089 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0173 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 a0002c0003t0035g0096 |
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 | a0002c0003t0035g0096 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0258 | 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 | a0001c0001t0004g0256 | 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 | a0001c0001t0019g0132 a0001c0008t0019g0124 |
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 | 211 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(208): 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 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0020g0134 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0250 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0009g0139 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0188 |
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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0021g0274 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | 7 | a0001c0001t0004g0003 a0001c0001t0004g0208 a0001c0001t0004g0246 others(4): 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 | a0001c0001t0001g0175 a0001c0001t0001g0232 a0001c0001t0004g0138 others(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 | a0002c0003t0035g0096 | 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0030g0204 | 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 | 28 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0002g0210 others(25): 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 | a0002c0002t0006g0030 a0002c0002t0006g0059 |
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 | a0002c0002t0003g0052 a0010c0010t0002g0239 |
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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0004g0277 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 |
259 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0004g0277 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | 46 | a0001c0001t0001g0203 a0001c0001t0001g0267 a0001c0001t0002g0141 others(43): Show |
46 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(43): 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 | a0002c0002t0003g0068 | 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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0003t0010g0106 | 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 | a0002c0002t0003g0044 a0002c0002t0017g0047 |
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 | a0002c0003t0034g0095 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0008t0012g0123 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0031g0254 a0002c0007t0016g0091 a0002c0007t0016g0092 |
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 | 45 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(42): Show |
46 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1936-2485T>C | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223371 | |||||||
| chr3:154223394 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0032g0135 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1936-2437G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223419 | |||||||
| chr3:154223594 | A | T | 208 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(205): 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | 46 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1936-1974T>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 10/14 | chr3 | 154223882 | |||||||
| chr3:154223975 | GA | G | 205 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(202): 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0002g0141 a0001c0015t0002g0142 a0002c0002t0010g0035 others(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 | 43 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(40): Show |
43 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(40): 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0029g0253 | 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 | a0002c0002t0005g0042 a0002c0002t0005g0043 |
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 | 113 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(110): 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 | a0002c0003t0016g0093 a0002c0003t0036g0094 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0002t0003g0048 a0002c0002t0003g0050 a0002c0002t0003g0055 |
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 | a0001c0001t0030g0204 | 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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): 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 | a0001c0001t0019g0132 a0001c0008t0019g0124 |
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 | a0001c0001t0029g0253 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0225 a0001c0001t0013g0125 a0001c0001t0015g0164 others(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 | a0001c0001t0002g0146 a0001c0001t0009g0139 a0001c0001t0009g0145 others(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 | a0001c0001t0001g0203 a0001c0001t0002g0224 a0001c0001t0002g0228 others(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 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0230 others(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 |
9 | a0001c0001t0002g0153 a0001c0001t0002g0190 a0001c0001t0002g0202 others(6): Show |
9 | HG00609.hp2 HG01168.hp2 HG01169.hp2 others(6): 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 | a0001c0001t0002g0141 a0001c0001t0002g0216 a0001c0001t0024g0152 others(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 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
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 | a0001c0001t0002g0257 a0002c0003t0016g0093 |
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 | 21 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(18): 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 | 177 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(174): 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 | a0001c0001t0001g0244 a0001c0001t0009g0237 a0004c0005t0001g0137 others(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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | 42 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(39): Show |
43 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(40): 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0007g0205 a0001c0001t0014g0133 a0001c0001t0031g0254 others(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 | a0001c0008t0012g0123 | 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 | 243 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0154 others(240): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): 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 | a0001c0001t0001g0147 a0001c0001t0001g0181 a0001c0001t0001g0193 others(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 | a0002c0003t0003g0090 a0002c0003t0005g0088 a0002c0003t0006g0089 |
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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0001g0147 | 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 | a0001c0001t0031g0254 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0007g0273 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2090+1696G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154227706 | |||||||
| chr3:154228136 | A | AT | 116 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(113): 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 | a0001c0001t0002g0234 a0001c0001t0007g0205 a0001c0001t0014g0133 others(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 | a0002c0003t0006g0101 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0041g0083 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0004g0138 | 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 | a0002c0002t0006g0029 a0002c0002t0006g0057 a0002c0002t0006g0064 |
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 | a0002c0002t0003g0071 | 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 | a0001c0001t0002g0231 | 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 | a0001c0001t0001g0244 a0001c0001t0009g0237 a0002c0003t0006g0102 others(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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
44 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(41): 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 | a0001c0001t0020g0134 | 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 | 211 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(208): 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0002c0002t0003g0067 | 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 | 265 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0002g0225 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0213 | 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 | a0002c0003t0017g0105 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0200 a0001c0001t0007g0143 a0001c0001t0007g0161 others(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 | a0001c0001t0001g0200 a0002c0002t0005g0061 a0002c0003t0005g0001 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0011g0261 | 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 | a0001c0001t0002g0230 | 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 | a0001c0001t0002g0238 a0001c0001t0002g0240 |
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 | a0002c0003t0003g0090 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0029g0253 | 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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2090+5499A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154231509 | |||||||
| chr3:154231654 | G | GT | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | 50 | a0001c0001t0001g0183 a0001c0001t0001g0203 a0001c0001t0002g0141 others(47): Show |
51 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(48): 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 | 254 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0004g0208 a0001c0001t0007g0177 a0001c0001t0013g0125 others(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 | a0002c0002t0040g0033 | 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 | a0001c0001t0002g0146 a0001c0001t0009g0145 a0003c0004t0009g0014 others(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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0002t0003g0080 | 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 | 44 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(41): Show |
45 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2090+6672A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154232682 | |||||||
| chr3:154232915 | A | C | 46 | a0001c0001t0001g0203 a0001c0001t0002g0141 a0001c0001t0002g0153 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(44): 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0020g0134 a0001c0008t0012g0123 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0004g0211 a0001c0001t0004g0212 |
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 | a0001c0001t0007g0205 a0001c0001t0014g0133 a0001c0001t0031g0254 others(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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0040g0033 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0003t0016g0093 a0002c0003t0036g0094 |
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 | a0001c0001t0002g0259 | 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 | a0001c0001t0002g0210 | 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 | a0001c0001t0021g0274 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0002c0003t0005g0117 | 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 | a0001c0001t0001g0244 a0001c0001t0009g0237 a0004c0005t0001g0137 others(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 | a0001c0001t0007g0213 | 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 | a0001c0001t0020g0134 | 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 | a0001c0001t0014g0133 a0001c0001t0031g0254 a0001c0006t0014g0129 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0032g0135 | 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 | a0001c0006t0014g0130 | 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 | a0001c0001t0028g0201 | 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 | a0001c0001t0001g0172 a0001c0001t0007g0219 a0001c0001t0011g0186 others(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 | a0001c0001t0007g0219 a0002c0002t0022g0078 a0002c0002t0022g0079 |
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 | a0001c0001t0007g0219 a0001c0001t0011g0186 a0001c0001t0015g0164 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0172 a0001c0001t0007g0219 a0001c0001t0011g0186 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0007g0205 a0001c0001t0030g0204 a0002c0003t0003g0099 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0011g0186 others(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 | a0001c0001t0002g0263 | 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 | a0001c0001t0032g0135 a0002c0003t0016g0093 a0002c0003t0036g0094 |
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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0001g0203 a0001c0001t0014g0133 a0001c0001t0031g0254 others(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 | a0001c0001t0014g0133 a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | 157 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(154): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): 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 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0183 |
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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0014g0133 a0001c0001t0031g0254 a0001c0006t0014g0129 others(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 | 111 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(108): 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 | a0001c0001t0007g0205 a0001c0001t0007g0273 a0001c0001t0030g0204 others(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 | a0002c0003t0034g0095 | 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 | a0006c0016t0001g0217 | 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 | a0001c0001t0001g0166 a0001c0001t0001g0180 a0001c0001t0001g0183 others(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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0151 | 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 | 1 | a0001c0001t0004g0003 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0187 |
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 | a0001c0001t0002g0240 a0001c0001t0002g0242 a0001c0001t0002g0247 others(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 | a0001c0001t0002g0238 a0001c0001t0004g0140 a0001c0001t0004g0218 others(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 | 34 | a0001c0001t0001g0180 a0001c0001t0001g0184 a0001c0001t0001g0200 others(31): Show |
35 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(32): 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 |
78 | a0001c0001t0001g0176 a0001c0001t0001g0203 a0001c0001t0001g0222 others(75): 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 |
57 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0173 others(54): 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 | a0001c0001t0001g0131 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0183 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0185 a0001c0001t0002g0153 a0001c0001t0012g0275 others(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 | a0001c0001t0012g0276 a0001c0008t0012g0123 a0002c0003t0006g0116 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | 180 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(177): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0001c0001t0001g0151 | 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 | a0002c0002t0040g0033 | 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 | 51 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0141 others(48): Show |
54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.2091-1422A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154238948 | |||||||
| chr3:154239023 | A | G | 181 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2091-1347A>G | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | chr3 | 154239023 | |||||||
| chr3:154239068 | T | G | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0002c0003t0005g0088 a0002c0003t0006g0089 a0002c0003t0006g0097 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0174 a0001c0001t0007g0177 others(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 | 137 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0154 others(134): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): 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 | a0005c0012t0008g0019 | 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 | a0001c0001t0029g0253 a0002c0003t0017g0105 |
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 | a0001c0001t0007g0273 a0001c0001t0015g0164 a0001c0009t0015g0162 others(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 | a0001c0001t0001g0157 a0002c0003t0005g0114 a0002c0003t0006g0089 |
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 | a0001c0001t0020g0134 a0002c0002t0003g0038 a0002c0002t0003g0065 others(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 | 50 | a0001c0001t0001g0172 a0001c0001t0001g0181 a0001c0001t0001g0191 others(47): 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 | a0001c0001t0007g0205 a0001c0001t0007g0213 a0001c0001t0007g0219 others(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 | 72 | a0001c0001t0001g0172 a0001c0001t0001g0181 a0001c0001t0001g0191 others(69): 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 | a0001c0001t0009g0237 a0003c0004t0009g0010 a0003c0004t0009g0014 others(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 | a0001c0008t0012g0123 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0171 a0001c0001t0019g0132 others(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 | a0001c0001t0007g0205 a0001c0001t0007g0213 a0001c0001t0007g0219 others(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 | a0001c0001t0020g0134 a0002c0002t0003g0038 a0002c0002t0003g0065 others(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 | a0001c0001t0007g0273 a0001c0001t0015g0164 a0001c0009t0015g0162 others(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 | a0001c0001t0015g0164 a0001c0001t0030g0204 a0001c0009t0015g0162 others(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 | a0001c0001t0015g0164 a0001c0001t0029g0253 a0001c0009t0015g0162 others(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 | a0005c0012t0008g0019 | 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 | a0001c0001t0002g0214 | 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 | a0002c0002t0017g0056 | 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 | a0002c0003t0036g0094 | 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 | a0002c0003t0016g0093 | 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 | a0002c0003t0035g0096 | 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 | a0001c0001t0018g0004 | 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 | a0001c0001t0001g0166 a0001c0001t0002g0216 |
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 | a0001c0001t0007g0171 a0002c0002t0003g0045 a0002c0002t0003g0084 others(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 | a0001c0001t0007g0174 a0001c0001t0007g0219 a0001c0001t0020g0209 others(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 | a0002c0007t0016g0091 | 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 | a0002c0003t0039g0100 | 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 | a0001c0001t0031g0254 a0002c0007t0016g0092 |
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 | a0001c0001t0002g0223 a0003c0004t0002g0008 |
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 | 40 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0141 others(37): Show |
42 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(39): 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 | a0001c0001t0002g0234 | 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 | a0002c0002t0003g0050 a0002c0002t0003g0072 a0002c0002t0003g0076 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0171 a0001c0001t0007g0174 others(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 | a0001c0001t0014g0133 | 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 | a0001c0006t0014g0129 a0001c0006t0014g0130 |
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 | a0001c0001t0004g0212 | 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 | a0001c0001t0001g0182 a0001c0001t0002g0266 a0001c0001t0002g0272 |
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 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
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 | a0002c0002t0003g0077 a0002c0002t0008g0082 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0171 a0001c0001t0007g0174 others(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 | a0001c0001t0007g0161 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 a0002c0003t0038g0098 |
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 | a0001c0001t0004g0277 a0001c0001t0028g0201 a0002c0003t0006g0116 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0171 a0001c0001t0007g0174 others(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 | a0002c0003t0034g0095 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0268 a0001c0001t0004g0156 others(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 | a0002c0003t0010g0103 | 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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0171 a0001c0001t0007g0174 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0183 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0250 a0001c0001t0004g0138 a0002c0002t0005g0028 others(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 | a0001c0001t0007g0143 a0001c0001t0007g0171 a0001c0001t0007g0174 others(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 | a0001c0001t0001g0147 a0001c0001t0004g0140 a0001c0001t0004g0208 others(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 | 23 | a0001c0001t0001g0157 a0001c0001t0001g0176 a0001c0001t0001g0185 others(20): 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 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0009g0139 a0002c0003t0006g0089 a0003c0004t0009g0010 others(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 | a0001c0008t0012g0123 | 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 | a0001c0001t0009g0145 a0002c0003t0006g0089 |
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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 |
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 | a0002c0003t0006g0089 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 |
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 | a0002c0003t0006g0089 | 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 | a0001c0001t0001g0147 a0001c0001t0004g0140 a0001c0001t0011g0186 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0199 a0001c0001t0001g0220 others(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 | a0002c0003t0005g0122 a0002c0003t0006g0101 |
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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0003t0003g0107 | 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
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 | a0001c0001t0004g0246 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0259 a0002c0003t0010g0106 |
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 | a0002c0003t0005g0104 a0002c0003t0005g0136 |
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 | a0002c0002t0005g0034 a0002c0002t0005g0042 a0002c0002t0005g0043 others(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 | a0008c0017t0002g0169 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0003g0062 a0007c0018t0007g0007 |
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 | a0002c0003t0006g0112 | 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 | a0001c0001t0020g0134 a0001c0001t0029g0253 |
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 | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2300+508C>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241087 | |||||||
| chr3:154241239 | G | T | 182 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(179): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0001c0001t0009g0139 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0014g0133 a0001c0001t0031g0254 a0001c0006t0014g0129 others(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 | a0001c0001t0012g0275 | 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 | a0001c0001t0009g0139 | 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 | a0001c0001t0004g0140 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2300+1212G>A | ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 12/14 | chr3 | 154241791 | |||||||
| chr3:154242300 | C | T | 1 | a0001c0001t0002g0189 | 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 | a0002c0003t0035g0096 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0259 a0002c0003t0010g0106 |
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 | 182 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(179): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0259 a0002c0003t0010g0106 |
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 | a0001c0001t0007g0171 a0002c0002t0003g0065 a0002c0002t0003g0085 |
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 | a0002c0002t0040g0033 | 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0020g0134 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0007g0205 a0001c0001t0007g0273 a0002c0003t0003g0090 others(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 | a0001c0001t0004g0148 | 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 | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0002g0189 | 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 | a0002c0002t0040g0033 | 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 | a0001c0001t0004g0246 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0020g0134 others(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 | a0002c0002t0040g0033 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0004g0149 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0002c0002t0003g0027 a0002c0002t0003g0072 a0002c0002t0003g0073 others(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 | a0002c0003t0005g0119 | 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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0002c0002t0006g0059 | 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 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
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 | 129 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(126): 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 | a0001c0001t0002g0235 | 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 | a0001c0001t0002g0189 | 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 | a0002c0002t0003g0067 | 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 | a0001c0001t0029g0253 | 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 | a0002c0003t0005g0088 a0002c0003t0006g0089 a0002c0003t0006g0097 others(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 | a0001c0001t0029g0253 | 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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | 51 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0141 others(48): Show |
54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0007g0174 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0029g0253 others(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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | 51 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0141 others(48): Show |
54 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(51): 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0002c0002t0040g0033 | 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 | a0002c0002t0003g0071 | 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 | a0001c0001t0007g0143 a0002c0002t0003g0037 a0002c0002t0003g0038 others(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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 |
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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0029g0253 | 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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0001g0252 | 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 | a0002c0003t0004g0086 a0002c0003t0004g0087 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0021g0274 | 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 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 |
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 | a0001c0001t0002g0238 a0001c0001t0002g0240 |
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 | a0002c0002t0040g0033 | 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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 others(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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 others(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 | a0001c0001t0002g0247 | 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 | a0002c0002t0003g0023 | 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 | a0001c0001t0001g0200 a0002c0002t0005g0061 a0002c0003t0005g0001 others(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 | a0001c0001t0009g0145 a0001c0001t0009g0237 a0003c0004t0009g0010 others(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 | a0001c0001t0001g0206 a0001c0001t0004g0207 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0002c0002t0040g0033 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 |
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 | a0002c0002t0008g0075 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0002c0003t0016g0093 a0002c0003t0035g0096 a0002c0003t0036g0094 others(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 | a0009c0011t0005g0018 | 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 | 203 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(200): 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 | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0019g0132 a0001c0008t0019g0124 |
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 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0200 a0002c0002t0005g0061 a0002c0003t0005g0001 others(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 | a0001c0001t0004g0140 a0001c0001t0004g0170 a0001c0001t0004g0218 others(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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0001t0029g0253 others(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 | a0001c0001t0030g0204 | 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 | a0001c0001t0021g0274 | 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0029g0253 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0029g0253 | 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 | a0002c0002t0040g0033 | 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 | a0002c0002t0006g0030 a0002c0002t0006g0049 a0002c0002t0006g0059 others(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 | a0002c0003t0005g0108 | 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 | a0001c0001t0012g0275 a0001c0001t0012g0276 a0001c0008t0012g0123 |
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 | a0001c0001t0001g0199 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0002g0223 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0032g0135 | 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 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
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 | a0001c0001t0029g0253 | 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 | 102 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(99): 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0007g0143 a0001c0001t0007g0161 a0001c0001t0007g0171 others(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 | a0001c0001t0021g0274 | 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 | a0002c0002t0003g0085 | 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 | 191 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): 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 | a0001c0001t0007g0205 a0001c0001t0007g0273 a0002c0003t0003g0090 others(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 | 184 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(181): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0002c0002t0041g0083 | 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 | a0001c0001t0015g0164 a0001c0009t0015g0162 a0001c0009t0015g0163 |
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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 | a0001c0001t0021g0274 | 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 | a0002c0002t0006g0029 a0002c0002t0006g0057 a0002c0002t0006g0064 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0259 a0002c0003t0010g0106 |
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 | a0002c0003t0005g0119 | 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 | 267 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0151 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0002g0263 | 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 | a0002c0002t0003g0025 a0002c0002t0003g0084 |
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 | a0002c0002t0003g0077 | 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 | a0001c0001t0029g0253 | 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 | a0001c0001t0013g0125 a0001c0001t0013g0127 a0001c0001t0013g0128 others(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 | a0001c0001t0019g0132 a0001c0001t0032g0135 a0001c0008t0019g0124 |
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 |