Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9181 |
| ensemblid | ENSG00000116584.22 |
| hgncid | 682 |
| symbol | ARHGEF2 |
| name | Rho/Rac guanine nucleotide exchange factor 2 |
| refseq_nuc | NM_001162383.2 |
| refseq_prot | NP_001155855.1 |
| ensembl_nuc | ENST00000361247.9 |
| ensembl_prot | ENSP00000354837.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 155946854 |
| end | 155978547 |
| strand | - |
| ver | v1.2 |
| region | chr1:155946854-155978547 |
| region5000 | chr1:155941854-155983547 |
| regionname0 | ARHGEF2_chr1_155946854_155978547 |
| regionname5000 | ARHGEF2_chr1_155941854_155983547 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 986 | 275 | 82 | 50 | 95 | 12 | 34 | 65 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | MSRIE others(981): Show |
chr1 | 155941854 | 155983547 |
| a0002 | 0/0 | 986 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | MSRIE others(981): Show |
chr1 | 155941854 | 155983547 |
| a0003 | 0/0 | 986 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | MSRIE others(981): Show |
chr1 | 155941854 | 155983547 |
| a0004 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | MSRIE others(981): Show |
chr1 | 155941854 | 155983547 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2958 | 269 | 78 | 49 | 94 | 12 | 34 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0001c0003 | 0/0 | 2958 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0001c0006 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0001c0007 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0002c0002 | 0/0 | 2958 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0003c0004 | 0/0 | 2958 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 | ||
| a0004c0005 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | ATGTC others(2953): Show |
chr1 | 155941854 | 155983547 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4169 | 257 | 77 | 47 | 92 | 9 | 30 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0002 | 0/0 | 4169 | 7 | 1 | 2 | 0 | 2 | 2 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0003 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0004 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0005 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0006 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0001t0007 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0003t0001 | 0/0 | 4169 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0006t0001 | 0/0 | 4169 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0001c0007t0001 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0002c0002t0001 | 0/0 | 4169 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0003c0004t0001 | 0/0 | 4169 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| a0004c0005t0001 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | GAGTC others(4164): Show |
chr1 | 155941854 | 155983547 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 9 | 4 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0002 | 1/0 | 11 | 9 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0003 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0010 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0001c0007t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0003c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| a0004c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0063 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | FIN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02809 | hp2 | a0004 | c0005 | t0001 | g0152 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0201 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18963 | hp1 | a0001 | c0006 | t0001 | g0095 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18985 | hp2 | a0003 | c0004 | t0001 | g0058 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19067 | hp1 | a0003 | c0004 | t0001 | g0066 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19077 | hp2 | a0003 | c0004 | t0001 | g0060 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ASW | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0140 | SAS | GIH | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0112 | AFR | MSL | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0105 | REF | REF | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | ARHGEF2_chr1_155941854_155983547 | ARHGEF2 | chr1 | 155941854 | 155983547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155947968 | C | A | 1 | a0003 | 3 | NA18985.hp2 NA19067.hp1 NA19077.hp2 |
missense_variant | MODERATE | c.2935G>T | p.Gly979Trp | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 3055/4169 | 2935/2961 | 979/986 | chr1 | 155947968 | |||
| chr1:155950335 | C | A | 1 | a0002 | 5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.2851G>T | p.Gly951Cys | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/22 | 2971/4169 | 2851/2961 | 951/986 | chr1 | 155950335 | |||
| chr1:155957716 | C | T | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1712G>A | p.Arg571His | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/22 | 1832/4169 | 1712/2961 | 571/986 | chr1 | 155957716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155950455 | G | A | 1 | a0001c0006 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.2731C>T | p.Leu911Leu | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/22 | 2851/4169 | 2731/2961 | 911/986 | chr1 | 155950455 | |||
| chr1:155951747 | C | A | 1 | a0001c0003 | 4 | HG01109.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.2202G>T | p.Pro734Pro | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 18/22 | 2322/4169 | 2202/2961 | 734/986 | chr1 | 155951747 | |||
| chr1:155961839 | G | A | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1290C>T | p.Asp430Asp | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/22 | 1410/4169 | 1290/2961 | 430/986 | chr1 | 155961839 | |||
| chr1:155965367 | T | C | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.516A>G | p.Ser172Ser | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/22 | 636/4169 | 516/2961 | 172/986 | chr1 | 155965367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155947129 | G | T | 1 | a0001c0001t0003 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 813 | chr1 | 155947129 | ||||||
| chr1:155947531 | G | A | 1 | a0001c0001t0004 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 411 | chr1 | 155947531 | ||||||
| chr1:155947598 | G | C | 2 | a0001c0001t0002 a0001c0001t0005 |
8 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 344 | chr1 | 155947598 | ||||||
| chr1:155947801 | T | A | 1 | a0001c0001t0005 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 141 | chr1 | 155947801 | ||||||
| chr1:155947920 | G | A | 1 | a0001c0001t0006 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 22 | chr1 | 155947920 | ||||||
| chr1:155947927 | G | C | 1 | a0001c0001t0007 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 22/22 | 15 | chr1 | 155947927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:155948089 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2888-74A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948089 | |||||||
| chr1:155948222 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2888-207G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948222 | |||||||
| chr1:155948365 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2888-350G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948365 | |||||||
| chr1:155948465 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2888-450T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948465 | |||||||
| chr1:155948563 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2888-548C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948563 | |||||||
| chr1:155948666 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2888-651A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948666 | |||||||
| chr1:155948793 | G | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2888-778C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948793 | |||||||
| chr1:155948828 | G | A | 11 | a0001c0001t0001g0026 a0001c0001t0001g0180 a0001c0001t0001g0187 others(8): Show |
12 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2888-813C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948828 | |||||||
| chr1:155948908 | C | T | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2888-893G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155948908 | |||||||
| chr1:155949264 | T | TAAATA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0062 others(5): Show |
10 | HG01243.hp1 HG01515.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.2887+1030_2887+103 others(9): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949264 | |||||||
| chr1:155949264 | T | TAAATAAA others(3): Show |
1 | a0001c0001t0001g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2887+1025_2887+103 others(14): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949264 | |||||||
| chr1:155949443 | G | A | 1 | a0001c0003t0001g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2887+856C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949443 | |||||||
| chr1:155949557 | C | T | 2 | a0001c0003t0001g0028 a0001c0003t0001g0197 |
3 | HG01109.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2887+742G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949557 | |||||||
| chr1:155949742 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2887+557G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949742 | |||||||
| chr1:155949743 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2887+556C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949743 | |||||||
| chr1:155949862 | G | A | 1 | a0001c0003t0001g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2887+437C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949862 | |||||||
| chr1:155949998 | G | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0069 others(1): Show |
5 | HG00544.hp1 HG02132.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2887+301C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155949998 | |||||||
| chr1:155950048 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2887+251G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 21/21 | chr1 | 155950048 | |||||||
| chr1:155950489 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0123 |
3 | HG01069.hp2 HG01071.hp2 HG01496.hp1 |
splice_region_variant&intron_variant | LOW | c.2704-7T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 20/21 | chr1 | 155950489 | |||||||
| chr1:155950574 | C | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2704-92G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 20/21 | chr1 | 155950574 | |||||||
| chr1:155952377 | G | A | 3 | a0001c0003t0001g0028 a0001c0003t0001g0197 a0001c0003t0001g0201 |
4 | HG01109.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1985-142C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 15/21 | chr1 | 155952377 | |||||||
| chr1:155952404 | C | T | 11 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0073 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1985-169G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 15/21 | chr1 | 155952404 | |||||||
| chr1:155953179 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1784-351G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953179 | |||||||
| chr1:155953265 | C | CA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1784-438dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953265 | |||||||
| chr1:155953265 | C | CAA | 6 | a0001c0001t0001g0082 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG00609.hp2 HG03195.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-439_1784-438d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953265 | |||||||
| chr1:155953692 | A | C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-864T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953692 | |||||||
| chr1:155953716 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1784-888G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953716 | |||||||
| chr1:155953746 | C | CA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0040 others(4): Show |
12 | HG01192.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784-919dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953746 | |||||||
| chr1:155953746 | CA | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0094 others(3): Show |
6 | HG02135.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1784-919delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953746 | |||||||
| chr1:155953763 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0147 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1784-935T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953763 | |||||||
| chr1:155953980 | G | T | 21 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0180 others(18): Show |
25 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1783+922C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155953980 | |||||||
| chr1:155954016 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1783+886G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954016 | |||||||
| chr1:155954085 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1783+817G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954085 | |||||||
| chr1:155954127 | A | AT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(2): Show |
9 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1783+774dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954127 | |||||||
| chr1:155954127 | A | ATT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(150): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1783+773_1783+774d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954127 | |||||||
| chr1:155954282 | C | CT | 26 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0045 others(23): Show |
26 | HG01496.hp2 HG01934.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1783+619dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954282 | |||||||
| chr1:155954282 | C | CTT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(60): Show |
80 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1783+618_1783+619d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954282 | |||||||
| chr1:155954285 | T | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1783+617A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954285 | |||||||
| chr1:155954323 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0210 |
3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1783+579C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954323 | |||||||
| chr1:155954328 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1783+574C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954328 | |||||||
| chr1:155954446 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+456T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954446 | |||||||
| chr1:155954478 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+424G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954478 | |||||||
| chr1:155954489 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+413G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954489 | |||||||
| chr1:155954519 | A | G | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1783+383T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954519 | |||||||
| chr1:155954521 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+381G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954521 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0001t0002g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0001t0002g0102 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0132 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(313): Show |
1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(322): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(314): Show |
15 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0053 others(12): Show |
15 | HG01168.hp1 HG01192.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783+312_1783+313i others(323): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954589 | A | ATCTACTT others(315): Show |
1 | a0001c0001t0001g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1783+312_1783+313i others(324): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954589 | |||||||
| chr1:155954613 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG02071.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1783+289T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954613 | |||||||
| chr1:155954631 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1783+271T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954631 | |||||||
| chr1:155954714 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1783+188T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954714 | |||||||
| chr1:155954755 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1783+147A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954755 | |||||||
| chr1:155954852 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1783+50A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 14/21 | chr1 | 155954852 | |||||||
| chr1:155955039 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1716-70A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955039 | |||||||
| chr1:155955074 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1716-105T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955074 | |||||||
| chr1:155955150 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0210 |
3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1716-181G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955150 | |||||||
| chr1:155955188 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0146 a0001c0001t0001g0151 others(1): Show |
4 | NA18985.hp1 NA19012.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716-219G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955188 | |||||||
| chr1:155955465 | T | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1716-496A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955465 | |||||||
| chr1:155955693 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1716-724G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955693 | |||||||
| chr1:155955779 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1716-810C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955779 | |||||||
| chr1:155955908 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1716-939C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155955908 | |||||||
| chr1:155956260 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0037 others(6): Show |
13 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1716-1291C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956260 | |||||||
| chr1:155956366 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0145 |
3 | HG02129.hp2 HG02132.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1715+1347G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956366 | |||||||
| chr1:155956426 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1715+1287G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956426 | |||||||
| chr1:155956609 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1715+1104T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956609 | |||||||
| chr1:155956887 | C | CA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1715+825dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956887 | |||||||
| chr1:155956887 | C | CAA | 35 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
42 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1715+824_1715+825d others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155956887 | |||||||
| chr1:155957038 | TA | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0198 |
6 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1715+674delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957038 | |||||||
| chr1:155957402 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1715+311G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957402 | |||||||
| chr1:155957421 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0182 others(4): Show |
8 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715+292A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957421 | |||||||
| chr1:155957459 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0215 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1715+254G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 13/21 | chr1 | 155957459 | |||||||
| chr1:155957899 | A | G | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-17T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957899 | |||||||
| chr1:155957950 | T | A | 1 | a0001c0003t0001g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1546-68A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957950 | |||||||
| chr1:155957961 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1546-79C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155957961 | |||||||
| chr1:155958053 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1546-171G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958053 | |||||||
| chr1:155958096 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1546-214G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958096 | |||||||
| chr1:155958170 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1545+150G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958170 | |||||||
| chr1:155958172 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1545+148C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958172 | |||||||
| chr1:155958194 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0092 others(11): Show |
18 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1545+126C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958194 | |||||||
| chr1:155958243 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0136 |
2 | NA18992.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1545+77G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958243 | |||||||
| chr1:155958282 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1545+38A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 12/21 | chr1 | 155958282 | |||||||
| chr1:155958441 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1469-45A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958441 | |||||||
| chr1:155958451 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1469-55G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958451 | |||||||
| chr1:155958574 | A | AT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(78): Show |
99 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1469-179dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958574 | |||||||
| chr1:155958679 | G | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1469-283C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155958679 | |||||||
| chr1:155959041 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0198 |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469-645A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959041 | |||||||
| chr1:155959664 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1469-1268G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959664 | |||||||
| chr1:155959701 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1469-1305A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959701 | |||||||
| chr1:155959705 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1469-1309A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959705 | |||||||
| chr1:155959771 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1469-1375G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959771 | |||||||
| chr1:155959853 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1469-1457G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959853 | |||||||
| chr1:155959882 | C | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.1469-1486G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959882 | |||||||
| chr1:155959910 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.1469-1514C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155959910 | |||||||
| chr1:155960068 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1468+1593A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960068 | |||||||
| chr1:155960468 | TA | T | 12 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0069 others(9): Show |
12 | HG01884.hp2 HG02132.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468+1192delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960468 | |||||||
| chr1:155960482 | A | AG | 75 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(72): Show |
92 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1468+1178_1468+117 others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960482 | |||||||
| chr1:155960482 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0109 a0001c0001t0001g0115 others(2): Show |
5 | HG01515.hp2 HG01981.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+1179T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960482 | |||||||
| chr1:155960766 | C | T | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+895G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960766 | |||||||
| chr1:155960987 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1468+674G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155960987 | |||||||
| chr1:155961059 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1468+602G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961059 | |||||||
| chr1:155961162 | T | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468+499A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961162 | |||||||
| chr1:155961194 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+467C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961194 | |||||||
| chr1:155961274 | C | CT | 7 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0136 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+386dupA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961274 | |||||||
| chr1:155961475 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1468+186A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961475 | |||||||
| chr1:155961577 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(71): Show |
91 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1468+84C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 11/21 | chr1 | 155961577 | |||||||
| chr1:155961999 | G | T | 1 | a0001c0003t0001g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1220-90C>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 10/21 | chr1 | 155961999 | |||||||
| chr1:155963211 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0182 others(3): Show |
7 | HG00140.hp2 HG01258.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-28A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963211 | |||||||
| chr1:155963261 | A | G | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.725-78T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963261 | |||||||
| chr1:155963344 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.725-162delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963344 | |||||||
| chr1:155963506 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0210 |
3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.725-323G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963506 | |||||||
| chr1:155963595 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.725-412G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963595 | |||||||
| chr1:155963675 | AT | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.725-493delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963675 | |||||||
| chr1:155963679 | T | A | 1 | a0001c0001t0002g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.725-496A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155963679 | |||||||
| chr1:155964018 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0119 |
2 | HG00099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.725-835C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964018 | |||||||
| chr1:155964032 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.725-849G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964032 | |||||||
| chr1:155964144 | CAA | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(58): Show |
77 | HG00280.hp2 HG00609.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.724+842_724+843del others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964144 | |||||||
| chr1:155964154 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+834T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964154 | |||||||
| chr1:155964155 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.724+833T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964155 | |||||||
| chr1:155964156 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+832T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964156 | |||||||
| chr1:155964157 | A | AATATATA others(27): Show |
1 | a0001c0001t0001g0130 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.724+830_724+831ins others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | |||||||
| chr1:155964157 | A | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0076 others(2): Show |
5 | HG00735.hp1 HG01516.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+831T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | |||||||
| chr1:155964157 | AAAAAAAA others(27): Show |
A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0006g0104 |
3 | NA18993.hp2 NA19054.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.724+797_724+830del others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964157 | |||||||
| chr1:155964158 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+830T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964158 | |||||||
| chr1:155964159 | A | AT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0092 others(6): Show |
13 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+828_724+829ins others(1): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | |||||||
| chr1:155964159 | A | ATATAT | 2 | a0001c0001t0001g0016 a0001c0001t0001g0064 |
3 | HG01070.hp2 HG01071.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.724+828_724+829ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | |||||||
| chr1:155964159 | A | T | 25 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(22): Show |
25 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.724+829T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | |||||||
| chr1:155964159 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0074 |
4 | HG00621.hp2 HG02083.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+811_724+828del others(18): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964159 | |||||||
| chr1:155964160 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.724+828T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964160 | |||||||
| chr1:155964160 | AAAAAAAA others(6): Show |
A | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+815_724+827del others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964160 | |||||||
| chr1:155964161 | A | ATATAT | 3 | a0001c0001t0001g0065 a0001c0001t0002g0102 a0003c0004t0001g0066 |
3 | HG01168.hp1 HG01168.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.724+826_724+827ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | |||||||
| chr1:155964161 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
164 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.724+827T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | |||||||
| chr1:155964161 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.724+815_724+826del others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964161 | |||||||
| chr1:155964162 | AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+815_724+825del others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964162 | |||||||
| chr1:155964163 | A | ATATAT | 3 | a0001c0001t0001g0089 a0001c0003t0001g0028 a0001c0003t0001g0197 |
4 | HG01109.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+824_724+825ins others(5): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | |||||||
| chr1:155964163 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.724+825T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | |||||||
| chr1:155964163 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.724+825T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964163 | |||||||
| chr1:155964164 | AAAAATAT others(4): Show |
A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0180 a0001c0001t0001g0187 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.724+813_724+823del others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964164 | |||||||
| chr1:155964164 | AAAAATAT others(6): Show |
A | 1 | a0001c0001t0001g0191 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.724+811_724+823del others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964164 | |||||||
| chr1:155964165 | A | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.724+823T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | |||||||
| chr1:155964165 | AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.724+803_724+822del others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | |||||||
| chr1:155964165 | AAAATATA others(15): Show |
A | 1 | a0001c0001t0001g0002 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.724+801_724+822del others(22): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964165 | |||||||
| chr1:155964167 | A | AAAAATAT others(36): Show |
1 | a0001c0001t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.724+820_724+821ins others(43): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AAAATATA others(11): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0210 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.724+820_724+821ins others(18): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.724+820_724+821ins others(20): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AAAATATA others(35): Show |
2 | a0002c0002t0001g0213 a0002c0002t0001g0214 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.724+820_724+821ins others(42): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AAAATATA others(39): Show |
1 | a0001c0001t0001g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.724+820_724+821ins others(46): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AAATATAT others(38): Show |
2 | a0002c0002t0001g0030 a0002c0002t0001g0209 |
3 | HG02896.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.724+820_724+821ins others(45): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AATAT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0027 others(3): Show |
7 | HG02055.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+817_724+820dup others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | AATATATA others(39): Show |
1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.724+820_724+821ins others(46): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964167 | A | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.724+821T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964167 | |||||||
| chr1:155964168 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.724+819_724+820ins others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964168 | |||||||
| chr1:155964169 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0198 |
7 | HG01891.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+819A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964169 | |||||||
| chr1:155964170 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724+818T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964170 | |||||||
| chr1:155964171 | T | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0198 |
4 | HG02922.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+817A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964171 | |||||||
| chr1:155964172 | A | ATATATG | 18 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
22 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.724+815_724+816ins others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964172 | |||||||
| chr1:155964174 | A | ATATATG | 4 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0049 others(1): Show |
5 | HG02630.hp2 HG03834.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+813_724+814ins others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | |||||||
| chr1:155964174 | A | ATATG | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(29): Show |
46 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.724+813_724+814ins others(4): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | |||||||
| chr1:155964174 | A | ATATGTAT others(27): Show |
1 | a0001c0001t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.724+813_724+814ins others(34): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | |||||||
| chr1:155964174 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
10 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+814T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964174 | |||||||
| chr1:155964175 | T | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+813A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964175 | |||||||
| chr1:155964176 | A | ATG | 17 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0038 others(14): Show |
20 | HG00099.hp1 HG00099.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.724+811_724+812ins others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964176 | |||||||
| chr1:155964176 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0092 others(11): Show |
18 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.724+812T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964176 | |||||||
| chr1:155964178 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.724+810T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964178 | |||||||
| chr1:155964180 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(64): Show |
83 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.724+808T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964180 | |||||||
| chr1:155964189 | T | C | 2 | a0001c0003t0001g0028 a0001c0003t0001g0197 |
3 | HG01109.hp1 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.724+799A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964189 | |||||||
| chr1:155964193 | TATATAC | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0183 |
3 | HG00140.hp2 HG01978.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.724+789_724+794del others(6): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964193 | |||||||
| chr1:155964195 | T | C | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+793A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964195 | |||||||
| chr1:155964196 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.724+792T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964196 | |||||||
| chr1:155964197 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.724+791A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964197 | |||||||
| chr1:155964199 | C | CAT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0119 |
3 | HG00099.hp2 HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.724+787_724+788dup others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | |||||||
| chr1:155964199 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0157 others(5): Show |
10 | HG00621.hp2 HG01975.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.724+789G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | |||||||
| chr1:155964199 | CAT | C | 3 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0191 |
3 | HG01258.hp1 HG02451.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.724+787_724+788del others(2): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964199 | |||||||
| chr1:155964201 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0183 others(1): Show |
5 | HG00140.hp2 HG01433.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.724+787A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964201 | |||||||
| chr1:155964202 | A | G | 1 | a0001c0001t0001g0007 | 3 | HG00621.hp2 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.724+786T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964202 | |||||||
| chr1:155964215 | TA | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0093 others(6): Show |
13 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.724+772delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964215 | |||||||
| chr1:155964216 | A | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0096 others(1): Show |
7 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.724+772T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964216 | |||||||
| chr1:155964227 | A | T | 1 | a0001c0001t0001g0007 | 3 | HG00621.hp2 HG02083.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.724+761T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964227 | |||||||
| chr1:155964641 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.724+347G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964641 | |||||||
| chr1:155964748 | C | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.724+240G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964748 | |||||||
| chr1:155964892 | CA | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.724+95delT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964892 | |||||||
| chr1:155964908 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0198 |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.724+80T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 7/21 | chr1 | 155964908 | |||||||
| chr1:155965141 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.581-10T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/21 | chr1 | 155965141 | |||||||
| chr1:155965141 | A | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.581-10T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 6/21 | chr1 | 155965141 | |||||||
| chr1:155965450 | G | A | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.471-38C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965450 | |||||||
| chr1:155965453 | C | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(73): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.471-41G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965453 | |||||||
| chr1:155965501 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471-89C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 5/21 | chr1 | 155965501 | |||||||
| chr1:155965893 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.341-133A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155965893 | |||||||
| chr1:155966009 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.341-249T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966009 | |||||||
| chr1:155966058 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.341-298A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966058 | |||||||
| chr1:155966236 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340+180G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966236 | |||||||
| chr1:155966359 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.340+57A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 4/21 | chr1 | 155966359 | |||||||
| chr1:155966910 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-23C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155966910 | |||||||
| chr1:155967002 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.209-115G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967002 | |||||||
| chr1:155967301 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-414C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967301 | |||||||
| chr1:155967371 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0036 others(14): Show |
21 | HG00438.hp1 HG00621.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.209-484T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967371 | |||||||
| chr1:155967599 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-712G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967599 | |||||||
| chr1:155967734 | A | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.209-847T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967734 | |||||||
| chr1:155967833 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.209-946G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155967833 | |||||||
| chr1:155968111 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.208+1045T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968111 | |||||||
| chr1:155968153 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.208+1003T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968153 | |||||||
| chr1:155968202 | CT | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.208+953delA | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968202 | |||||||
| chr1:155968284 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+872G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968284 | |||||||
| chr1:155968361 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.208+795A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968361 | |||||||
| chr1:155968740 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.208+416T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155968740 | |||||||
| chr1:155969084 | G | GA | 4 | a0002c0002t0001g0030 a0002c0002t0001g0209 a0002c0002t0001g0213 others(1): Show |
5 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+71dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 2/21 | chr1 | 155969084 | |||||||
| chr1:155969445 | G | A | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-145C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969445 | |||||||
| chr1:155969458 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-158T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969458 | |||||||
| chr1:155969585 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-285T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969585 | |||||||
| chr1:155969825 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-525G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969825 | |||||||
| chr1:155969886 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0111 |
3 | HG00280.hp2 HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.64-586C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155969886 | |||||||
| chr1:155970064 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.64-764C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970064 | |||||||
| chr1:155970373 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-1073G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970373 | |||||||
| chr1:155970472 | C | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-1172G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970472 | |||||||
| chr1:155970486 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-1186C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970486 | |||||||
| chr1:155970942 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-1642G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970942 | |||||||
| chr1:155970972 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-1672T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155970972 | |||||||
| chr1:155971157 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(96): Show |
122 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.64-1857A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971157 | |||||||
| chr1:155971300 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-2000C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971300 | |||||||
| chr1:155971387 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.64-2087C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971387 | |||||||
| chr1:155971579 | C | CA | 9 | a0001c0001t0001g0082 a0001c0001t0001g0196 a0001c0001t0001g0212 others(6): Show |
10 | HG00280.hp1 HG01192.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2280dupT | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | |||||||
| chr1:155971579 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0120 others(3): Show |
6 | HG00280.hp2 HG01496.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-2290_64-2280dup others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | |||||||
| chr1:155971579 | C | CAAAAAAA others(5): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(79): Show |
104 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.64-2291_64-2280dup others(12): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | |||||||
| chr1:155971579 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0163 others(4): Show |
7 | HG02622.hp1 HG03669.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2292_64-2280dup others(13): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971579 | |||||||
| chr1:155971706 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64-2406C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971706 | |||||||
| chr1:155971789 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.64-2489A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971789 | |||||||
| chr1:155971842 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.64-2542C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971842 | |||||||
| chr1:155971883 | T | TAAAAAAA others(4): Show |
1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2594_64-2584dup others(11): Show |
ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971883 | |||||||
| chr1:155971894 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(84): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.64-2594T>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971894 | |||||||
| chr1:155971902 | C | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2602G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971902 | |||||||
| chr1:155971904 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.64-2604A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971904 | |||||||
| chr1:155971912 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2612A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971912 | |||||||
| chr1:155971914 | T | C | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-2614A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155971914 | |||||||
| chr1:155972080 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.64-2780A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972080 | |||||||
| chr1:155972184 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64-2884A>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972184 | |||||||
| chr1:155972904 | A | G | 11 | a0001c0001t0001g0026 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-3604T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155972904 | |||||||
| chr1:155973003 | A | C | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-3703T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973003 | |||||||
| chr1:155973488 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-4188T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973488 | |||||||
| chr1:155973517 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02015.hp1 HG02083.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4217C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973517 | |||||||
| chr1:155973659 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.64-4359A>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973659 | |||||||
| chr1:155973732 | C | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-4432G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155973732 | |||||||
| chr1:155974398 | T | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(94): Show |
119 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.63+3967A>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974398 | |||||||
| chr1:155974524 | C | T | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+3841G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974524 | |||||||
| chr1:155974552 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+3813C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974552 | |||||||
| chr1:155974587 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.63+3778C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974587 | |||||||
| chr1:155974835 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0025 others(18): Show |
26 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+3530C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974835 | |||||||
| chr1:155974852 | A | AG | 72 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(69): Show |
89 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.63+3512dupC | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974852 | |||||||
| chr1:155974979 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.63+3386G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155974979 | |||||||
| chr1:155975073 | A | G | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+3292T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975073 | |||||||
| chr1:155975210 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
5 | HG01891.hp1 HG02145.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3155G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975210 | |||||||
| chr1:155975567 | C | G | 1 | a0001c0007t0001g0112 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+2798G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975567 | |||||||
| chr1:155975618 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+2747G>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155975618 | |||||||
| chr1:155976224 | C | G | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG00280.hp2 HG01074.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2141G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976224 | |||||||
| chr1:155976382 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.63+1983G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976382 | |||||||
| chr1:155976608 | A | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(95): Show |
120 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+1757T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976608 | |||||||
| chr1:155976750 | A | C | 1 | a0001c0001t0006g0104 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.63+1615T>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155976750 | |||||||
| chr1:155977635 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+730T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977635 | |||||||
| chr1:155977742 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+623C>G | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977742 | |||||||
| chr1:155977844 | G | A | 4 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG00099.hp1 HG01168.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+521C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977844 | |||||||
| chr1:155977884 | C | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
10 | HG00741.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+481G>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977884 | |||||||
| chr1:155977907 | C | T | 1 | a0001c0001t0001g0015 | 2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.63+458G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155977907 | |||||||
| chr1:155978009 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.63+356C>T | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978009 | |||||||
| chr1:155978084 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0023 others(83): Show |
104 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.63+281T>C | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978084 | |||||||
| chr1:155978139 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.63+226G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978139 | |||||||
| chr1:155978187 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+178G>A | ARHGEF2 | ENSG00000116584.22 | transcript | ENST00000361247.9 | protein_coding | 1/21 | chr1 | 155978187 |