Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9459 |
| ensemblid | ENSG00000129675.16 |
| hgncid | 685 |
| symbol | ARHGEF6 |
| name | Rac/Cdc42 guanine nucleotide exchange factor 6 |
| refseq_nuc | NM_004840.3 |
| refseq_prot | NP_004831.1 |
| ensembl_nuc | ENST00000250617.7 |
| ensembl_prot | ENSP00000250617.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 136665550 |
| end | 136780932 |
| strand | - |
| ver | v1.2 |
| region | chrX:136665550-136780932 |
| region5000 | chrX:136660550-136785932 |
| regionname0 | ARHGEF6_chrX_136665550_136780932 |
| regionname5000 | ARHGEF6_chrX_136660550_136785932 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 776 | 240 | 64 | 45 | 99 | 7 | 23 | 76 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| a0002 | 0/0 | 776 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| a0003 | 0/0 | 776 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| a0004 | 0/0 | 776 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| a0005 | 0/0 | 776 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| a0006 | 0/0 | 776 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | MNPEE others(771): Show |
chrX | 136660550 | 136785932 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2328 | 235 | 60 | 45 | 99 | 7 | 22 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0001c0002 | 0/0 | 2328 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0001c0006 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0002c0004 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0003c0003 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0004c0008 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0005c0005 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 | ||
| a0006c0007 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | ATGAA others(2323): Show |
chrX | 136660550 | 136785932 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4860 | 204 | 54 | 39 | 85 | 6 | 18 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0002 | 0/0 | 4860 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0003 | 0/0 | 4860 | 6 | 0 | 2 | 4 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0004 | 0/0 | 4860 | 5 | 2 | 1 | 1 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0005 | 0/0 | 4860 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0006 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0007 | 0/0 | 4860 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0008 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0010 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0011 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0012 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0013 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0014 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0015 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0001t0016 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0002t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0002t0002 | 0/0 | 4860 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0001c0006t0001 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0002c0004t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0002c0004t0009 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0003c0003t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0003c0003t0002 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0004c0008t0006 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0005c0005t0001 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| a0006c0007t0001 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | AGTCC others(4855): Show |
chrX | 136660550 | 136785932 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0010g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0001t0016g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0001c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0002c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0002c0004t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0003c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0003c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0004c0008t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0005c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| a0006c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0031 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0117 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0194 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02451 | hp1 | a0002 | c0004 | t0009 | g0174 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0002 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0130 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0182 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03239 | hp1 | a0004 | c0008 | t0006 | g0084 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03688 | hp1 | a0001 | c0006 | t0001 | g0038 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0066 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03942 | hp1 | a0001 | c0001 | t0016 | g0097 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0191 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18949 | hp2 | a0001 | c0001 | t0015 | g0135 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18980 | hp1 | a0005 | c0005 | t0001 | g0092 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19058 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19076 | hp1 | a0006 | c0007 | t0001 | g0125 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0229 | AFR | ASW | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0039 | EUR | TSI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | USA | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0111 | AFR | USA | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0030 | REF | REF | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0126 | REF | REF | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136681946 | G | A | 1 | a0003 | 2 | HG02976.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.1502C>T | p.Thr501Met | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/22 | 1552/4860 | 1502/2331 | 501/776 | chrX | 136681946 | |||
| chrX:136682832 | G | C | 1 | a0006 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.1405C>G | p.Arg469Gly | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/22 | 1455/4860 | 1405/2331 | 469/776 | chrX | 136682832 | |||
| chrX:136687987 | G | C | 1 | a0004 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1190C>G | p.Thr397Ser | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/22 | 1240/4860 | 1190/2331 | 397/776 | chrX | 136687987 | |||
| chrX:136708707 | C | A | 1 | a0002 | 2 | HG02451.hp1 HG02809.hp2 |
missense_variant | MODERATE | c.891G>T | p.Gln297His | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/22 | 941/4860 | 891/2331 | 297/776 | chrX | 136708707 | |||
| chrX:136732149 | C | T | 1 | a0005 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.685G>A | p.Val229Ile | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/22 | 735/4860 | 685/2331 | 229/776 | chrX | 136732149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136675035 | G | A | 1 | a0001c0002 | 4 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.2007C>T | p.Ser669Ser | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/22 | 2057/4860 | 2007/2331 | 669/776 | chrX | 136675035 | |||
| chrX:136679627 | A | G | 1 | a0001c0006 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1738T>C | p.Leu580Leu | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/22 | 1788/4860 | 1738/2331 | 580/776 | chrX | 136679627 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136665560 | G | A | 1 | a0001c0001t0013 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2469 | chrX | 136665560 | ||||||
| chrX:136665627 | A | T | 1 | a0001c0001t0012 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2402T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2402 | chrX | 136665627 | ||||||
| chrX:136665634 | G | C | 2 | a0001c0001t0006 a0004c0008t0006 |
2 | HG03239.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2395C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2395 | chrX | 136665634 | ||||||
| chrX:136665683 | G | A | 1 | a0001c0001t0003 | 6 | HG00423.hp1 HG00741.hp2 HG01952.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2346C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2346 | chrX | 136665683 | ||||||
| chrX:136665881 | C | T | 1 | a0001c0001t0011 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2148G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2148 | chrX | 136665881 | ||||||
| chrX:136665947 | A | C | 1 | a0001c0001t0010 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2082 | chrX | 136665947 | ||||||
| chrX:136665975 | T | C | 1 | a0001c0001t0014 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2054 | chrX | 136665975 | ||||||
| chrX:136666008 | T | C | 1 | a0001c0001t0004 | 5 | HG02148.hp1 NA18971.hp1 NA19030.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2021A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2021 | chrX | 136666008 | ||||||
| chrX:136666352 | A | T | 1 | a0002c0004t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1677 | chrX | 136666352 | ||||||
| chrX:136666888 | C | A | 3 | a0001c0001t0002 a0001c0002t0002 a0003c0003t0002 |
8 | HG01243.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1141G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1141 | chrX | 136666888 | ||||||
| chrX:136667389 | T | C | 1 | a0001c0001t0015 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 640 | chrX | 136667389 | ||||||
| chrX:136667484 | G | A | 1 | a0001c0001t0007 | 2 | HG02071.hp1 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 545 | chrX | 136667484 | ||||||
| chrX:136667779 | T | C | 1 | a0001c0001t0016 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 250 | chrX | 136667779 | ||||||
| chrX:136667850 | G | A | 1 | a0001c0001t0005 | 5 | HG02129.hp1 NA18953.hp1 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*179C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 179 | chrX | 136667850 | ||||||
| chrX:136780898 | A | C | 1 | a0001c0001t0008 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/22 | 16 | chrX | 136780898 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:136668204 | G | T | 1 | a0001c0001t0015g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2191-35C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668204 | |||||||
| chrX:136668467 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(64): Show |
68 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.2191-298A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668467 | |||||||
| chrX:136668512 | T | TTTC | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0019 others(41): Show |
45 | HG00323.hp2 HG01243.hp1 HG02056.hp1 others(42): Show |
intron_variant | MODIFIER | c.2191-346_2191-344d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668512 | |||||||
| chrX:136668512 | T | TTTCTTC | 22 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0050 others(19): Show |
22 | HG00639.hp2 HG01168.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.2191-349_2191-344d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668512 | |||||||
| chrX:136668512 | T | TTTCTTCT others(2): Show |
5 | a0001c0001t0001g0077 a0001c0001t0001g0086 a0001c0001t0001g0113 others(2): Show |
5 | HG00438.hp1 HG02559.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-352_2191-344d others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668512 | |||||||
| chrX:136668512 | T | TTTCTTCT others(5): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0224 a0001c0001t0003g0143 others(1): Show |
4 | HG00423.hp1 HG01167.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2191-355_2191-344d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668512 | |||||||
| chrX:136668512 | T | TTTCTTCT others(11): Show |
1 | a0001c0001t0003g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2191-361_2191-344d others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668512 | |||||||
| chrX:136668524 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0020 |
2 | NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2191-355G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668524 | |||||||
| chrX:136668527 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0020 |
2 | NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2191-358G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668527 | |||||||
| chrX:136668530 | C | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(8): Show |
11 | HG00673.hp1 HG02896.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.2191-361G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668530 | |||||||
| chrX:136668533 | C | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(39): Show |
42 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.2191-364G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668533 | C | CTTA | 8 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0070 others(5): Show |
8 | HG02055.hp1 HG03225.hp1 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.2191-367_2191-365d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668533 | C | CTTATTA | 8 | a0001c0001t0001g0053 a0001c0001t0001g0218 a0001c0001t0001g0235 others(5): Show |
8 | HG01261.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2191-370_2191-365d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668533 | C | CTTCTTA | 5 | a0001c0001t0001g0022 a0001c0001t0001g0056 a0001c0001t0001g0063 others(2): Show |
5 | HG02615.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-365_2191-364i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668533 | CTTA | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0088 others(22): Show |
25 | HG00323.hp2 HG01891.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.2191-367_2191-365d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668533 | CTTATTA | C | 9 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0106 others(6): Show |
9 | HG00423.hp1 HG01167.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2191-370_2191-365d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | |||||||
| chrX:136668536 | A | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0023 others(46): Show |
49 | HG00438.hp2 HG00639.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.2191-367T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668536 | |||||||
| chrX:136668539 | A | C | 20 | a0001c0001t0001g0034 a0001c0001t0001g0062 a0001c0001t0001g0068 others(17): Show |
20 | HG00639.hp1 HG01952.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.2191-370T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668539 | |||||||
| chrX:136668542 | A | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG01952.hp1 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2191-373T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668542 | |||||||
| chrX:136668675 | T | C | 2 | a0001c0002t0002g0128 a0003c0003t0002g0111 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2191-506A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668675 | |||||||
| chrX:136669004 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2190+478A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136669004 | |||||||
| chrX:136669005 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0204 |
2 | HG00438.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2190+477C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136669005 | |||||||
| chrX:136669263 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2190+219A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136669263 | |||||||
| chrX:136669793 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2136-257G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136669793 | |||||||
| chrX:136669927 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2136-391G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136669927 | |||||||
| chrX:136670076 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2136-540G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136670076 | |||||||
| chrX:136670357 | A | C | 1 | a0001c0001t0014g0191 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2136-821T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136670357 | |||||||
| chrX:136670649 | G | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2136-1113C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136670649 | |||||||
| chrX:136671573 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2135+447A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136671573 | |||||||
| chrX:136671658 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2135+362T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136671658 | |||||||
| chrX:136671775 | T | C | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2135+245A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136671775 | |||||||
| chrX:136671955 | C | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2135+65G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136671955 | |||||||
| chrX:136672225 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2036-106A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136672225 | |||||||
| chrX:136672226 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2036-107G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136672226 | |||||||
| chrX:136672333 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2036-214G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136672333 | |||||||
| chrX:136672910 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2036-791G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136672910 | |||||||
| chrX:136672942 | A | G | 22 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2036-823T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136672942 | |||||||
| chrX:136673000 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2036-881G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136673000 | |||||||
| chrX:136673235 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2036-1116C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136673235 | |||||||
| chrX:136673871 | G | T | 22 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2035+1136C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136673871 | |||||||
| chrX:136673959 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0010g0117 |
2 | HG01496.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2035+1048G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136673959 | |||||||
| chrX:136674733 | A | G | 1 | a0001c0001t0010g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2035+274T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136674733 | |||||||
| chrX:136674787 | A | G | 22 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2035+220T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136674787 | |||||||
| chrX:136674920 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2035+87G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136674920 | |||||||
| chrX:136675134 | A | G | 1 | a0001c0002t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1946-38T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675134 | |||||||
| chrX:136675226 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1946-130G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675226 | |||||||
| chrX:136675356 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1946-260C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675356 | |||||||
| chrX:136675496 | C | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): Show |
47 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1946-400G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675496 | |||||||
| chrX:136675552 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1946-456G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675552 | |||||||
| chrX:136675602 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1946-506C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675602 | |||||||
| chrX:136675616 | C | T | 1 | a0001c0001t0013g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1946-520G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675616 | |||||||
| chrX:136675669 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1946-573G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675669 | |||||||
| chrX:136675742 | G | A | 1 | a0001c0001t0010g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1946-646C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675742 | |||||||
| chrX:136676376 | G | A | 4 | a0001c0002t0001g0118 a0001c0002t0002g0114 a0001c0002t0002g0128 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1945+248C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136676376 | |||||||
| chrX:136677353 | T | C | 1 | a0006c0007t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1851+583A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677353 | |||||||
| chrX:136677481 | A | G | 1 | a0001c0001t0004g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1851+455T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677481 | |||||||
| chrX:136677860 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18949.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1851+76C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677860 | |||||||
| chrX:136677880 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0005 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1851+56C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677880 | |||||||
| chrX:136678149 | C | T | 3 | a0001c0001t0004g0039 a0001c0001t0004g0096 a0001c0001t0004g0112 |
3 | HG02148.hp1 NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1831-193G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678149 | |||||||
| chrX:136678241 | A | G | 22 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1831-285T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678241 | |||||||
| chrX:136678395 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1831-439G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678395 | |||||||
| chrX:136678443 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1831-487G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678443 | |||||||
| chrX:136678795 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1830+740A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678795 | |||||||
| chrX:136679395 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+140T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136679395 | |||||||
| chrX:136679869 | A | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1705-209T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 15/21 | chrX | 136679869 | |||||||
| chrX:136680114 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1705-454A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 15/21 | chrX | 136680114 | |||||||
| chrX:136680621 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1704+110A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 15/21 | chrX | 136680621 | |||||||
| chrX:136681128 | T | G | 1 | a0001c0001t0015g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1559-252A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681128 | |||||||
| chrX:136681178 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1559-302C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681178 | |||||||
| chrX:136681229 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1559-353G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681229 | |||||||
| chrX:136681563 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1558+327C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681563 | |||||||
| chrX:136681666 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1558+224C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681666 | |||||||
| chrX:136681971 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0005 |
2 | HG02630.hp1 HG02818.hp2 |
splice_region_variant&intron_variant | LOW | c.1480-3T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136681971 | |||||||
| chrX:136682133 | A | T | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1480-165T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682133 | |||||||
| chrX:136682267 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1480-299A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682267 | |||||||
| chrX:136682329 | G | C | 20 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(17): Show |
20 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1480-361C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682329 | |||||||
| chrX:136682504 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1479+254A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682504 | |||||||
| chrX:136682716 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1479+42G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682716 | |||||||
| chrX:136682928 | A | T | 1 | a0001c0001t0014g0191 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1393-84T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682928 | |||||||
| chrX:136682974 | T | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0127 a0001c0001t0001g0181 |
3 | HG02572.hp1 NA18962.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1393-130A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682974 | |||||||
| chrX:136682975 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1393-131T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682975 | |||||||
| chrX:136683208 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1393-364A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683208 | |||||||
| chrX:136683362 | C | CT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0079 others(27): Show |
31 | HG02055.hp1 HG02080.hp1 HG02148.hp1 others(28): Show |
intron_variant | MODIFIER | c.1393-519dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683362 | |||||||
| chrX:136683427 | C | T | 1 | a0001c0001t0004g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1393-583G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683427 | |||||||
| chrX:136683502 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
102 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1393-658T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683502 | |||||||
| chrX:136683911 | G | A | 1 | a0001c0001t0003g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1393-1067C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683911 | |||||||
| chrX:136684097 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1393-1253T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136684097 | |||||||
| chrX:136684195 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1393-1351G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136684195 | |||||||
| chrX:136684430 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1392+1247C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136684430 | |||||||
| chrX:136684564 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1392+1113G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136684564 | |||||||
| chrX:136684760 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1392+917C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136684760 | |||||||
| chrX:136685006 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1392+671G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685006 | |||||||
| chrX:136685103 | G | T | 1 | a0001c0001t0010g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1392+574C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685103 | |||||||
| chrX:136685157 | T | C | 16 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
16 | HG00323.hp2 HG00438.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1392+520A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685157 | |||||||
| chrX:136685177 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1392+500G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685177 | |||||||
| chrX:136685206 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1392+471G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685206 | |||||||
| chrX:136685533 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1392+144C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685533 | |||||||
| chrX:136685579 | C | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+98G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685579 | |||||||
| chrX:136685604 | C | CA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0099 a0001c0001t0001g0100 others(19): Show |
22 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1392+72dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685604 | |||||||
| chrX:136685604 | CA | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0042 others(9): Show |
12 | HG01168.hp1 HG01261.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1392+72delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685604 | |||||||
| chrX:136686421 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1246-598A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686421 | |||||||
| chrX:136686517 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-694G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686517 | |||||||
| chrX:136686518 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-695G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686518 | |||||||
| chrX:136686519 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-696T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686519 | |||||||
| chrX:136686521 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-698C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686521 | |||||||
| chrX:136686523 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-700T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686523 | |||||||
| chrX:136686525 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-702T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686525 | |||||||
| chrX:136686527 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-704T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686527 | |||||||
| chrX:136686528 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-705A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686528 | |||||||
| chrX:136686531 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-708G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686531 | |||||||
| chrX:136686533 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-710C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686533 | |||||||
| chrX:136686534 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-711A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686534 | |||||||
| chrX:136686541 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-718T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686541 | |||||||
| chrX:136686542 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-719G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686542 | |||||||
| chrX:136686543 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-720T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686543 | |||||||
| chrX:136686544 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-721G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686544 | |||||||
| chrX:136686548 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-725C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686548 | |||||||
| chrX:136686552 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0010g0117 |
2 | HG01496.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1246-729C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686552 | |||||||
| chrX:136686553 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-730C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686553 | |||||||
| chrX:136686557 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-734C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686557 | |||||||
| chrX:136686558 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-735T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686558 | |||||||
| chrX:136686564 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-741G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686564 | |||||||
| chrX:136686566 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-743A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686566 | |||||||
| chrX:136686568 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-745G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686568 | |||||||
| chrX:136686582 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-759C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686582 | |||||||
| chrX:136686584 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-761C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686584 | |||||||
| chrX:136686586 | ATG | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0205 a0001c0001t0002g0003 |
3 | HG01496.hp1 HG01981.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1246-765_1246-764d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686586 | |||||||
| chrX:136686586 | ATGTGTG | A | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1246-769_1246-764d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686586 | |||||||
| chrX:136686588 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-765C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686588 | |||||||
| chrX:136686588 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1246-789_1246-766d others(26): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686588 | |||||||
| chrX:136686588 | GTGTGTGT others(19): Show |
G | 3 | a0001c0001t0001g0105 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1246-791_1246-766d others(28): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686588 | |||||||
| chrX:136686589 | TGTGTGTA others(27): Show |
T | 1 | a0001c0001t0010g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1246-800_1246-767d others(36): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686589 | |||||||
| chrX:136686590 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-767C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686590 | |||||||
| chrX:136686592 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-769C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686592 | G | GTA | 4 | a0001c0001t0001g0109 a0001c0001t0001g0237 a0001c0001t0004g0039 others(1): Show |
4 | HG02976.hp1 HG03225.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-770_1246-769i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686592 | G | GTATA | 3 | a0001c0001t0001g0236 a0001c0001t0001g0242 a0001c0001t0014g0191 |
3 | HG03098.hp1 HG03195.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1246-770_1246-769i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686592 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1246-770_1246-769i others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686592 | GTGTATA | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0225 others(5): Show |
9 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1246-775_1246-770d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686592 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0001g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1246-779_1246-770d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686592 | |||||||
| chrX:136686594 | G | A | 24 | a0001c0001t0001g0079 a0001c0001t0001g0093 a0001c0001t0001g0104 others(21): Show |
24 | HG02055.hp1 HG02080.hp1 HG02148.hp1 others(21): Show |
intron_variant | MODIFIER | c.1246-771C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686594 | G | GTA | 23 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0052 others(20): Show |
23 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1246-773_1246-772d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686594 | G | GTATA | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1246-775_1246-772d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686594 | G | GTATATA | 5 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0149 others(2): Show |
5 | HG00140.hp1 HG00673.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-777_1246-772d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686594 | G | GTGTATAT others(29): Show |
1 | a0001c0001t0001g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1246-772_1246-771i others(38): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686594 | GTA | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0053 others(8): Show |
11 | HG01071.hp2 HG01109.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1246-773_1246-772d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | |||||||
| chrX:136686595 | T | TATATATA others(23): Show |
2 | a0001c0001t0003g0243 a0001c0001t0003g0246 |
2 | HG00741.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1246-802_1246-773d others(32): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686595 | |||||||
| chrX:136686596 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0216 |
2 | HG01106.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1246-773T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686596 | |||||||
| chrX:136686597 | T | TATATATA others(21): Show |
4 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0060 others(1): Show |
4 | HG01175.hp1 HG03669.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-802_1246-775d others(30): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686597 | |||||||
| chrX:136686598 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1246-775T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686598 | |||||||
| chrX:136686599 | T | TATATATA others(17): Show |
1 | a0001c0001t0003g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1246-777_1246-776i others(26): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686599 | |||||||
| chrX:136686607 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-784A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686607 | |||||||
| chrX:136686609 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-786A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686609 | |||||||
| chrX:136686611 | TATATATA others(5): Show |
T | 1 | a0001c0001t0008g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1246-800_1246-789d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686611 | |||||||
| chrX:136686612 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-789T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686612 | |||||||
| chrX:136686614 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-791T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686614 | |||||||
| chrX:136686615 | TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1246-802_1246-793d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686615 | |||||||
| chrX:136686619 | TATAC | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0083 a0001c0001t0001g0235 |
3 | HG02738.hp1 HG03041.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1246-800_1246-797d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686619 | |||||||
| chrX:136686619 | TATACACA others(17): Show |
T | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1246-820_1246-797d others(26): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686619 | |||||||
| chrX:136686621 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0217 a0001c0001t0002g0005 |
3 | HG02559.hp1 HG02818.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1246-798A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686621 | |||||||
| chrX:136686621 | TACACATA others(15): Show |
T | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG02809.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-820_1246-799d others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686621 | |||||||
| chrX:136686623 | C | T | 54 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0063 others(51): Show |
54 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1246-800G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686623 | |||||||
| chrX:136686625 | C | T | 14 | a0001c0001t0001g0105 a0001c0001t0001g0216 a0001c0001t0001g0219 others(11): Show |
14 | HG01496.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1246-802G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686625 | |||||||
| chrX:136686625 | CAT | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0098 a0001c0001t0001g0129 others(4): Show |
7 | HG00642.hp1 HG01496.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1246-804_1246-803d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686625 | |||||||
| chrX:136686627 | T | C | 49 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(46): Show |
49 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1246-804A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686627 | |||||||
| chrX:136686627 | T | TATATATA others(15): Show |
1 | a0001c0001t0002g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1246-805_1246-804i others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686627 | |||||||
| chrX:136686627 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0241 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1246-805_1246-804i others(28): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686627 | |||||||
| chrX:136686627 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1246-805_1246-804i others(30): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686627 | |||||||
| chrX:136686629 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0233 a0001c0001t0004g0234 |
3 | HG02055.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1246-806A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | |||||||
| chrX:136686629 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1246-807_1246-806i others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | |||||||
| chrX:136686630 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1246-843_1246-808d others(38): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686630 | |||||||
| chrX:136686631 | T | C | 2 | a0001c0002t0002g0114 a0001c0002t0002g0128 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1246-808A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686631 | |||||||
| chrX:136686641 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0235 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1246-818A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686641 | |||||||
| chrX:136686641 | TAC | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0220 a0001c0001t0001g0222 others(8): Show |
12 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1246-820_1246-819d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686641 | |||||||
| chrX:136686643 | C | T | 25 | a0001c0001t0001g0079 a0001c0001t0001g0093 a0001c0001t0001g0104 others(22): Show |
25 | HG01496.hp2 HG02055.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.1246-820G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686643 | |||||||
| chrX:136686647 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0004g0039 a0001c0001t0004g0096 others(1): Show |
4 | HG02148.hp1 NA19240.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-824G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686647 | |||||||
| chrX:136686681 | CAT | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0098 others(2): Show |
5 | HG00642.hp1 HG01168.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-860_1246-859d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686681 | |||||||
| chrX:136686682 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1246-860_1246-859i others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686682 | |||||||
| chrX:136686693 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02074.hp1 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-870A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686693 | |||||||
| chrX:136686697 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02074.hp1 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-874G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686697 | |||||||
| chrX:136686697 | CATATATA others(21): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1246-902_1246-875d others(30): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686697 | |||||||
| chrX:136686705 | T | TAC | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 |
3 | HG02080.hp2 NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1246-883_1246-882i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686705 | |||||||
| chrX:136686707 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0222 a0001c0002t0002g0114 |
3 | HG02074.hp1 HG02818.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1246-884A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686707 | |||||||
| chrX:136686709 | C | CAT | 34 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0063 others(31): Show |
34 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1246-888_1246-887d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686709 | C | CATAT | 5 | a0001c0001t0001g0067 a0001c0001t0001g0173 a0001c0001t0001g0176 others(2): Show |
5 | HG02683.hp1 HG03669.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-890_1246-887d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686709 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02074.hp1 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-886G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686709 | CAT | C | 119 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0019 others(116): Show |
119 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1246-888_1246-887d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686709 | CATAT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0085 others(9): Show |
12 | HG00423.hp1 HG01168.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1246-890_1246-887d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686709 | CATATATA others(1): Show |
C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0079 others(23): Show |
27 | HG02055.hp1 HG02080.hp1 HG02148.hp1 others(24): Show |
intron_variant | MODIFIER | c.1246-894_1246-887d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686709 | |||||||
| chrX:136686711 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1246-888A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686711 | |||||||
| chrX:136686717 | T | TATATACA others(13): Show |
1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1246-895_1246-894i others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686717 | |||||||
| chrX:136687297 | C | T | 46 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1245+635G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136687297 | |||||||
| chrX:136687376 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1245+556C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136687376 | |||||||
| chrX:136687448 | T | C | 20 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0121 others(17): Show |
20 | HG02015.hp1 HG02071.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1245+484A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136687448 | |||||||
| chrX:136687613 | A | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0079 others(27): Show |
31 | HG02055.hp1 HG02080.hp1 HG02148.hp1 others(28): Show |
intron_variant | MODIFIER | c.1245+319T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136687613 | |||||||
| chrX:136688104 | G | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0085 others(1): Show |
4 | HG01168.hp1 HG01168.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186-113C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688104 | |||||||
| chrX:136688444 | G | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1186-453C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688444 | |||||||
| chrX:136688539 | G | A | 1 | a0001c0001t0007g0194 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1186-548C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688539 | |||||||
| chrX:136688549 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1186-558G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688549 | |||||||
| chrX:136688558 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1186-567G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688558 | |||||||
| chrX:136688736 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1186-745G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688736 | |||||||
| chrX:136688975 | T | A | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1186-984A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136688975 | |||||||
| chrX:136689099 | A | C | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1186-1108T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136689099 | |||||||
| chrX:136689229 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1186-1238G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136689229 | |||||||
| chrX:136690279 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1185+331A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136690279 | |||||||
| chrX:136690549 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1185+61C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136690549 | |||||||
| chrX:136691200 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-452G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691200 | |||||||
| chrX:136691201 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-453T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691201 | |||||||
| chrX:136691203 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-455C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691203 | |||||||
| chrX:136691205 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-457C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691205 | |||||||
| chrX:136691206 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-458G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691206 | |||||||
| chrX:136691209 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-461T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691209 | |||||||
| chrX:136691210 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-462T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691210 | |||||||
| chrX:136691213 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-465T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691213 | |||||||
| chrX:136691215 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-467T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691215 | |||||||
| chrX:136691218 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-470T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691218 | |||||||
| chrX:136691220 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-472A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691220 | |||||||
| chrX:136691225 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-477T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691225 | |||||||
| chrX:136691229 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-481A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691229 | |||||||
| chrX:136691230 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-482A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691230 | |||||||
| chrX:136691233 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-485T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691233 | |||||||
| chrX:136691235 | C | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-487G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691235 | |||||||
| chrX:136691236 | A | AAGTGATT others(24): Show |
1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-489_1047-488i others(33): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691236 | |||||||
| chrX:136691248 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-500A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691248 | |||||||
| chrX:136691256 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-508T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691256 | |||||||
| chrX:136691301 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-553T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691301 | |||||||
| chrX:136691327 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-579T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691327 | |||||||
| chrX:136691330 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-582G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691330 | |||||||
| chrX:136691331 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-583T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691331 | |||||||
| chrX:136691349 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-601T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691349 | |||||||
| chrX:136691358 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-610T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691358 | |||||||
| chrX:136691371 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-623A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691371 | |||||||
| chrX:136691389 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-641T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691389 | |||||||
| chrX:136691396 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-648A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691396 | |||||||
| chrX:136691943 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1047-1195G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691943 | |||||||
| chrX:136692032 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1047-1284T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136692032 | |||||||
| chrX:136692297 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0079 others(25): Show |
29 | HG02055.hp1 HG02080.hp1 HG02148.hp1 others(26): Show |
intron_variant | MODIFIER | c.1047-1549C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136692297 | |||||||
| chrX:136692381 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1047-1633G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136692381 | |||||||
| chrX:136693336 | C | A | 4 | a0001c0001t0001g0222 a0001c0001t0004g0039 a0001c0001t0004g0112 others(1): Show |
4 | NA18971.hp1 NA18991.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047-2588G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693336 | |||||||
| chrX:136693566 | G | A | 46 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1047-2818C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693566 | |||||||
| chrX:136693654 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0145 |
2 | HG02735.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1047-2906A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693654 | |||||||
| chrX:136693797 | C | T | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-3049G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693797 | |||||||
| chrX:136694056 | C | CT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(30): Show |
34 | HG00738.hp1 HG01109.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.1047-3309dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694056 | |||||||
| chrX:136694056 | C | CTT | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1047-3310_1047-330 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694056 | |||||||
| chrX:136694198 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1047-3450C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694198 | |||||||
| chrX:136694361 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0088 |
2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1047-3613T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694361 | |||||||
| chrX:136694716 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1047-3968C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694716 | |||||||
| chrX:136695353 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1047-4605G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136695353 | |||||||
| chrX:136695659 | C | T | 1 | a0001c0001t0016g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1047-4911G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136695659 | |||||||
| chrX:136695758 | C | G | 1 | a0001c0001t0011g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047-5010G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136695758 | |||||||
| chrX:136695942 | C | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1047-5194G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136695942 | |||||||
| chrX:136696097 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1047-5349C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696097 | |||||||
| chrX:136696166 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1047-5418T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696166 | |||||||
| chrX:136696445 | C | A | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1047-5697G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696445 | |||||||
| chrX:136696683 | G | A | 4 | a0001c0002t0001g0118 a0001c0002t0002g0114 a0001c0002t0002g0128 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-5935C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696683 | |||||||
| chrX:136696846 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0013g0031 |
2 | HG01099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1047-6098G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696846 | |||||||
| chrX:136697150 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047-6402G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136697150 | |||||||
| chrX:136697281 | A | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1047-6533T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136697281 | |||||||
| chrX:136697311 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1047-6563T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136697311 | |||||||
| chrX:136697374 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1047-6626C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136697374 | |||||||
| chrX:136697425 | A | G | 3 | a0001c0002t0001g0118 a0001c0002t0002g0114 a0001c0002t0002g0132 |
3 | HG02818.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1047-6677T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136697425 | |||||||
| chrX:136698050 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
99 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1047-7302G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698050 | |||||||
| chrX:136698250 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1047-7502A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698250 | |||||||
| chrX:136698419 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1047-7671C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698419 | |||||||
| chrX:136698437 | A | G | 3 | a0001c0002t0001g0118 a0001c0002t0002g0114 a0001c0002t0002g0132 |
3 | HG02818.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1047-7689T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698437 | |||||||
| chrX:136698841 | T | C | 1 | a0001c0002t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1046+8067A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698841 | |||||||
| chrX:136698858 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1046+8050C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698858 | |||||||
| chrX:136699437 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1046+7471G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699437 | |||||||
| chrX:136699542 | T | C | 2 | a0001c0001t0002g0211 a0001c0001t0002g0212 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1046+7366A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699542 | |||||||
| chrX:136699599 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1046+7309C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699599 | |||||||
| chrX:136699995 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0079 others(24): Show |
28 | HG02055.hp1 HG02080.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1046+6913A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699995 | |||||||
| chrX:136700107 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0012g0177 |
2 | NA18968.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1046+6801A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700107 | |||||||
| chrX:136700181 | G | T | 1 | a0001c0001t0001g0017 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6727C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700181 | |||||||
| chrX:136700248 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1046+6660C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700248 | |||||||
| chrX:136700387 | C | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+6521G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700387 | |||||||
| chrX:136700707 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0235 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1046+6201A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700707 | |||||||
| chrX:136700777 | C | A | 2 | a0001c0001t0007g0119 a0001c0001t0007g0194 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1046+6131G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700777 | |||||||
| chrX:136700887 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1046+6021T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700887 | |||||||
| chrX:136700901 | G | A | 1 | a0003c0003t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1046+6007C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700901 | |||||||
| chrX:136700976 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0010g0117 |
2 | HG01496.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1046+5932C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700976 | |||||||
| chrX:136701108 | A | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+5800T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701108 | |||||||
| chrX:136701336 | G | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+5572C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701336 | |||||||
| chrX:136701375 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1046+5533G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701375 | |||||||
| chrX:136701401 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1046+5507T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701401 | |||||||
| chrX:136701621 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1046+5287T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701621 | |||||||
| chrX:136701702 | C | CT | 12 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0061 others(9): Show |
12 | HG00438.hp1 HG01175.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+5205dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | |||||||
| chrX:136701702 | CT | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02818.hp1 HG02922.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1046+5205delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | |||||||
| chrX:136701702 | CTT | C | 14 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(11): Show |
14 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1046+5204_1046+520 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | |||||||
| chrX:136701702 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1046+5190_1046+520 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | |||||||
| chrX:136701768 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1046+5140G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701768 | |||||||
| chrX:136701776 | T | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+5132A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701776 | |||||||
| chrX:136701793 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+5115G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701793 | |||||||
| chrX:136701804 | T | G | 1 | a0001c0001t0001g0017 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5104A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701804 | |||||||
| chrX:136701809 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5099C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701809 | |||||||
| chrX:136701810 | C | G | 1 | a0001c0001t0001g0017 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5098G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701810 | |||||||
| chrX:136701853 | G | A | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+5055C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701853 | |||||||
| chrX:136701857 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1046+5051T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701857 | |||||||
| chrX:136701860 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1046+5048T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701860 | |||||||
| chrX:136701869 | G | A | 1 | a0001c0001t0010g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1046+5039C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701869 | |||||||
| chrX:136701936 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1046+4972A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701936 | |||||||
| chrX:136701989 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00323.hp1 HG01081.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046+4919C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701989 | |||||||
| chrX:136702102 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | NA18982.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1046+4806A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702102 | |||||||
| chrX:136702258 | G | A | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+4650C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702258 | |||||||
| chrX:136702451 | T | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+4457A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702451 | |||||||
| chrX:136702941 | A | C | 1 | a0001c0001t0001g0032 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1046+3967T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702941 | |||||||
| chrX:136702960 | C | T | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+3948G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702960 | |||||||
| chrX:136702996 | A | G | 1 | a0001c0001t0016g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1046+3912T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702996 | |||||||
| chrX:136703009 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1046+3899T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703009 | |||||||
| chrX:136703102 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1046+3806A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703102 | |||||||
| chrX:136703165 | T | C | 1 | a0001c0001t0014g0191 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1046+3743A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703165 | |||||||
| chrX:136703186 | C | T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+3722G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703186 | |||||||
| chrX:136703276 | A | G | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+3632T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703276 | |||||||
| chrX:136703292 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1046+3616G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703292 | |||||||
| chrX:136703525 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1046+3383A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703525 | |||||||
| chrX:136703583 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0088 |
2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1046+3325G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703583 | |||||||
| chrX:136703654 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1046+3254G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703654 | |||||||
| chrX:136703710 | T | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+3198A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703710 | |||||||
| chrX:136703765 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1046+3143C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703765 | |||||||
| chrX:136703902 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1046+3006C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703902 | |||||||
| chrX:136704083 | T | C | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1046+2825A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704083 | |||||||
| chrX:136704176 | C | T | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0005g0148 others(4): Show |
7 | HG02129.hp1 NA18612.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046+2732G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704176 | |||||||
| chrX:136704313 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1046+2595G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704313 | |||||||
| chrX:136704507 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1046+2401C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704507 | |||||||
| chrX:136704683 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1046+2225C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704683 | |||||||
| chrX:136704807 | A | G | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1046+2101T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704807 | |||||||
| chrX:136704991 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1046+1917C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704991 | |||||||
| chrX:136705096 | G | A | 1 | a0004c0008t0006g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1046+1812C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705096 | |||||||
| chrX:136705268 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0145 |
2 | HG02735.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1046+1640G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705268 | |||||||
| chrX:136705355 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1046+1553G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705355 | |||||||
| chrX:136705426 | T | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0006g0066 |
3 | HG03492.hp1 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1046+1482A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705426 | |||||||
| chrX:136705440 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1046+1468A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705440 | |||||||
| chrX:136705793 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1046+1115C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705793 | |||||||
| chrX:136705809 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1046+1099C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705809 | |||||||
| chrX:136706227 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1046+681G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136706227 | |||||||
| chrX:136706425 | T | C | 1 | a0001c0001t0004g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1046+483A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136706425 | |||||||
| chrX:136707423 | C | T | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.924-393G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136707423 | |||||||
| chrX:136708182 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0244 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+493C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708182 | |||||||
| chrX:136708201 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.923+474A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708201 | |||||||
| chrX:136708322 | T | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+353A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708322 | |||||||
| chrX:136708357 | T | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+318A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708357 | |||||||
| chrX:136708381 | TA | T | 12 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
12 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+293delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708381 | |||||||
| chrX:136708804 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.828-34A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136708804 | |||||||
| chrX:136708829 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0244 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.828-59C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136708829 | |||||||
| chrX:136708838 | T | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-68A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136708838 | |||||||
| chrX:136709034 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.828-264A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136709034 | |||||||
| chrX:136709129 | C | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-359G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136709129 | |||||||
| chrX:136709269 | A | ATTTG | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.828-503_828-500dup others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136709269 | |||||||
| chrX:136709738 | G | T | 1 | a0001c0002t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.828-968C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136709738 | |||||||
| chrX:136710041 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.828-1271G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710041 | |||||||
| chrX:136710330 | C | CAT | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(16): Show |
19 | HG01167.hp1 HG01261.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.828-1562_828-1561d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATAT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0063 a0001c0001t0001g0159 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.828-1564_828-1561d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATATAT | 53 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0032 others(50): Show |
53 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.828-1566_828-1561d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATATATA others(1): Show |
23 | a0001c0001t0001g0061 a0001c0001t0001g0120 a0001c0001t0001g0121 others(20): Show |
23 | HG00280.hp1 HG00621.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.828-1568_828-1561d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATATATA others(3): Show |
16 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0160 others(13): Show |
16 | HG00423.hp2 HG01496.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.828-1570_828-1561d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATATATA others(5): Show |
1 | a0001c0001t0005g0171 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.828-1572_828-1561d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18612.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.828-1574_828-1561d others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710330 | CAT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(38): Show |
42 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.828-1562_828-1561d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | |||||||
| chrX:136710448 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-1678C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710448 | |||||||
| chrX:136710537 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0014g0191 |
2 | HG02080.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.828-1767G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710537 | |||||||
| chrX:136710631 | C | G | 1 | a0001c0002t0002g0132 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.828-1861G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710631 | |||||||
| chrX:136710828 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.828-2058T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710828 | |||||||
| chrX:136711008 | G | A | 1 | a0001c0002t0002g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.828-2238C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711008 | |||||||
| chrX:136711138 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.827+2138G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711138 | |||||||
| chrX:136711466 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.827+1810T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711466 | |||||||
| chrX:136711619 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.827+1657C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711619 | |||||||
| chrX:136711875 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0173 |
2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.827+1401C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711875 | |||||||
| chrX:136711945 | T | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.827+1331A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711945 | |||||||
| chrX:136711984 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.827+1292C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136711984 | |||||||
| chrX:136712255 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+1021A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136712255 | |||||||
| chrX:136712478 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.827+798T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136712478 | |||||||
| chrX:136713782 | A | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-412T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136713782 | |||||||
| chrX:136713815 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733-445A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136713815 | |||||||
| chrX:136714373 | T | C | 1 | a0003c0003t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733-1003A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714373 | |||||||
| chrX:136714533 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-1163C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714533 | |||||||
| chrX:136714577 | A | G | 1 | a0001c0001t0004g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.733-1207T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714577 | |||||||
| chrX:136714864 | A | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0228 a0001c0001t0001g0236 others(2): Show |
5 | HG02976.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1494T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714864 | |||||||
| chrX:136714922 | A | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0228 a0001c0001t0001g0236 others(2): Show |
5 | HG02976.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1552T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714922 | |||||||
| chrX:136715044 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.733-1674C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136715044 | |||||||
| chrX:136715074 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.733-1704C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136715074 | |||||||
| chrX:136715376 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-2006G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136715376 | |||||||
| chrX:136716015 | A | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-2645T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136716015 | |||||||
| chrX:136716576 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-3206T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136716576 | |||||||
| chrX:136716725 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.733-3355C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136716725 | |||||||
| chrX:136717022 | G | A | 1 | a0006c0007t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.733-3652C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717022 | |||||||
| chrX:136717107 | A | C | 2 | a0001c0001t0001g0222 a0001c0001t0004g0223 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.733-3737T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717107 | |||||||
| chrX:136717489 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-4119T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717489 | |||||||
| chrX:136717882 | A | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0067 others(94): Show |
97 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.733-4512T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717882 | |||||||
| chrX:136717950 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.733-4580G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717950 | |||||||
| chrX:136717958 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.733-4588C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717958 | |||||||
| chrX:136717975 | G | C | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.733-4605C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717975 | |||||||
| chrX:136718323 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0149 |
2 | HG00673.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.733-4953G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136718323 | |||||||
| chrX:136718330 | T | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0067 others(94): Show |
97 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.733-4960A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136718330 | |||||||
| chrX:136718418 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.733-5048C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136718418 | |||||||
| chrX:136718504 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(201): Show |
205 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.733-5134A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136718504 | |||||||
| chrX:136718730 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.733-5360T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136718730 | |||||||
| chrX:136719004 | T | TA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(50): Show |
54 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.733-5635dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719004 | |||||||
| chrX:136719004 | TA | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0050 others(16): Show |
19 | HG00609.hp1 HG01168.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.733-5635delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719004 | |||||||
| chrX:136719626 | A | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0087 others(1): Show |
4 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-6256T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719626 | |||||||
| chrX:136720093 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.733-6723G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720093 | |||||||
| chrX:136720199 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG01167.hp1 HG01261.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-6829G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720199 | |||||||
| chrX:136720356 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733-6986T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720356 | |||||||
| chrX:136720483 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.733-7113G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720483 | |||||||
| chrX:136720505 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.733-7135C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720505 | |||||||
| chrX:136720507 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733-7137T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720507 | |||||||
| chrX:136720541 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.733-7171G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720541 | |||||||
| chrX:136720652 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.733-7282A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720652 | |||||||
| chrX:136720683 | G | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0225 others(5): Show |
9 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-7313C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720683 | |||||||
| chrX:136720852 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.733-7482A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720852 | |||||||
| chrX:136720944 | A | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0067 others(93): Show |
96 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.733-7574T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720944 | |||||||
| chrX:136721022 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.733-7652A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136721022 | |||||||
| chrX:136721106 | C | A | 13 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0137 others(10): Show |
13 | HG00423.hp2 HG01934.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.733-7736G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136721106 | |||||||
| chrX:136721565 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-8195T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136721565 | |||||||
| chrX:136722067 | A | T | 2 | a0001c0001t0001g0232 a0001c0001t0003g0241 |
2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.733-8697T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136722067 | |||||||
| chrX:136722402 | A | AATATTTG others(17): Show |
1 | a0001c0001t0001g0161 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.733-9056_733-9033d others(26): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136722402 | |||||||
| chrX:136723007 | C | T | 12 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0137 others(9): Show |
12 | HG00423.hp2 HG01934.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+9095G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723007 | |||||||
| chrX:136723262 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.732+8840A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723262 | |||||||
| chrX:136723314 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0005 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.732+8788T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723314 | |||||||
| chrX:136723320 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+8782C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723320 | |||||||
| chrX:136723558 | G | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0005 others(4): Show |
7 | HG01496.hp2 HG02818.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+8544C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723558 | |||||||
| chrX:136723690 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+8412C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723690 | |||||||
| chrX:136723737 | A | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+8365T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723737 | |||||||
| chrX:136723928 | C | CA | 7 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG01167.hp1 HG01261.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+8173dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136723928 | |||||||
| chrX:136724078 | C | CT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0033 others(5): Show |
8 | HG01346.hp2 HG02148.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+8023dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724078 | |||||||
| chrX:136724161 | C | T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
5 | NA18991.hp1 NA19007.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+7941G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724161 | |||||||
| chrX:136724455 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.732+7647T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724455 | |||||||
| chrX:136724798 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+7304G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724798 | |||||||
| chrX:136724844 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+7258C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724844 | |||||||
| chrX:136725101 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732+7001A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725101 | |||||||
| chrX:136725216 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732+6886T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725216 | |||||||
| chrX:136725299 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+6803C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725299 | |||||||
| chrX:136725363 | G | GC | 13 | a0001c0001t0001g0073 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
13 | HG01891.hp1 HG01993.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+6738dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725363 | |||||||
| chrX:136725371 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.732+6731G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725371 | |||||||
| chrX:136725373 | C | CA | 10 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0053 others(7): Show |
10 | HG01261.hp1 HG01934.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+6728dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725373 | |||||||
| chrX:136725781 | G | A | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.732+6321C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725781 | |||||||
| chrX:136726060 | A | G | 5 | a0001c0001t0005g0148 a0001c0001t0005g0152 a0001c0001t0005g0153 others(2): Show |
5 | HG02129.hp1 NA18953.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+6042T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726060 | |||||||
| chrX:136726264 | G | GTCCTTAG others(6): Show |
1 | a0001c0001t0006g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.732+5825_732+5837d others(15): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726264 | |||||||
| chrX:136726299 | CCATTATC others(23): Show |
C | 1 | a0001c0001t0001g0020 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.732+5773_732+5802d others(32): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726299 | |||||||
| chrX:136726424 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.732+5678T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726424 | |||||||
| chrX:136726660 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.732+5442C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726660 | |||||||
| chrX:136726688 | T | C | 1 | a0001c0001t0015g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.732+5414A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726688 | |||||||
| chrX:136727305 | G | GTCTT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
33 | HG00438.hp2 HG01109.hp1 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.732+4793_732+4796d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727305 | |||||||
| chrX:136727305 | GTCTTTCT others(15): Show |
G | 18 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0064 others(15): Show |
18 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.732+4775_732+4796d others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727305 | |||||||
| chrX:136727305 | GTCTTTCT others(19): Show |
G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0080 others(1): Show |
4 | HG01952.hp1 HG02155.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4771_732+4796d others(28): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727305 | |||||||
| chrX:136727307 | CTTTCTTT others(11): Show |
C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0027 others(5): Show |
8 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+4777_732+4794d others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727307 | |||||||
| chrX:136727311 | CTTTCTTT others(7): Show |
C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0065 others(3): Show |
6 | HG00323.hp2 HG01261.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+4777_732+4790d others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727311 | |||||||
| chrX:136727315 | CTTTCTTT others(3): Show |
C | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0198 others(2): Show |
5 | HG00639.hp1 HG01346.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+4777_732+4786d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727315 | |||||||
| chrX:136727319 | CTTTCTT | C | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0076 others(7): Show |
10 | HG01433.hp1 HG02451.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+4777_732+4782d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727319 | |||||||
| chrX:136727323 | CTT | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0091 others(6): Show |
9 | HG01167.hp1 HG01496.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+4777_732+4778d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727323 | |||||||
| chrX:136727323 | CTTTTTCT others(13): Show |
C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+4759_732+4778d others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727323 | |||||||
| chrX:136727325 | T | TTCTC | 4 | a0001c0001t0001g0137 a0001c0001t0001g0156 a0001c0001t0001g0160 others(1): Show |
4 | HG01934.hp1 NA18968.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4776_732+4777i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | T | TTCTTTTT others(1): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0099 others(14): Show |
17 | HG00323.hp1 HG00621.hp1 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.732+4776_732+4777i others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | T | TTCTTTTT others(5): Show |
18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0059 others(15): Show |
18 | HG00140.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.732+4776_732+4777i others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | T | TTCTTTTT others(9): Show |
6 | a0001c0001t0001g0057 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02647.hp1 HG03834.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4776_732+4777i others(18): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | TTTTC | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0028 others(3): Show |
6 | HG00639.hp2 HG01346.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4773_732+4776d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | TTTTCTTT others(1): Show |
T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(10): Show |
13 | HG00642.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+4769_732+4776d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | TTTTCTTT others(5): Show |
T | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.732+4765_732+4776d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727325 | TTTTCTTT others(9): Show |
T | 1 | a0001c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.732+4761_732+4776d others(18): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | |||||||
| chrX:136727327 | T | C | 70 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0050 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.732+4775A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727327 | |||||||
| chrX:136727329 | C | T | 62 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0052 others(59): Show |
62 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.732+4773G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727329 | |||||||
| chrX:136727331 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0179 a0001c0001t0002g0212 |
3 | HG01243.hp1 HG01981.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.732+4771A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727331 | |||||||
| chrX:136727331 | TTC | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0091 others(5): Show |
8 | HG01167.hp1 HG01496.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+4769_732+4770d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727331 | |||||||
| chrX:136727335 | T | C | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.732+4767A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727335 | |||||||
| chrX:136727335 | TTC | T | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0076 others(7): Show |
10 | HG01433.hp1 HG02451.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+4765_732+4766d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727335 | |||||||
| chrX:136727339 | T | C | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.732+4763A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727339 | |||||||
| chrX:136727339 | TTC | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0198 others(2): Show |
5 | HG00639.hp1 HG01346.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+4761_732+4762d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727339 | |||||||
| chrX:136727343 | TTC | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0065 others(3): Show |
6 | HG00323.hp2 HG01261.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+4757_732+4758d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727343 | |||||||
| chrX:136727347 | TTC | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0027 others(5): Show |
8 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+4753_732+4754d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727347 | |||||||
| chrX:136727351 | TTC | T | 18 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0064 others(15): Show |
18 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.732+4749_732+4750d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727351 | |||||||
| chrX:136727355 | T | TTCTTTCT others(45): Show |
1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.732+4695_732+4746d others(54): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727355 | |||||||
| chrX:136727355 | TTC | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0080 others(1): Show |
4 | HG01952.hp1 HG02155.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4745_732+4746d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727355 | |||||||
| chrX:136727369 | CTTTCTTT others(19): Show |
C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0081 |
2 | HG01258.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.732+4707_732+4732d others(28): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727369 | |||||||
| chrX:136727373 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.732+4712_732+4728d others(19): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727373 | |||||||
| chrX:136727373 | CTTTCTTT others(11): Show |
C | 2 | a0001c0001t0001g0089 a0001c0001t0016g0097 |
2 | HG02965.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.732+4711_732+4728d others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727373 | |||||||
| chrX:136727373 | CTTTCTTT others(15): Show |
C | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.732+4707_732+4728d others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727373 | |||||||
| chrX:136727381 | CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.732+4711_732+4720d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727381 | |||||||
| chrX:136727381 | CTTTCTTT others(7): Show |
C | 1 | a0001c0001t0001g0017 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+4707_732+4720d others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727381 | |||||||
| chrX:136727385 | CTTTCTTT others(3): Show |
C | 6 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0162 others(3): Show |
6 | HG00741.hp1 HG01256.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4707_732+4716d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727385 | |||||||
| chrX:136727387 | TTCTTTCT others(3): Show |
T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0161 |
3 | HG01175.hp2 NA18939.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.732+4705_732+4714d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727387 | |||||||
| chrX:136727389 | CTTTCTT | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0192 a0001c0001t0001g0199 others(3): Show |
6 | HG01928.hp1 HG02015.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4707_732+4712d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727389 | |||||||
| chrX:136727391 | T | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG01167.hp1 HG01261.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+4711A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727391 | |||||||
| chrX:136727393 | CTT | C | 7 | a0001c0001t0001g0131 a0001c0001t0001g0138 a0001c0001t0001g0142 others(4): Show |
7 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+4707_732+4708d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727393 | |||||||
| chrX:136727395 | T | C | 73 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(70): Show |
73 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.732+4707A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | |||||||
| chrX:136727395 | T | TC | 3 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0204 |
3 | NA18977.hp1 NA18988.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.732+4706_732+4707i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | |||||||
| chrX:136727395 | T | TTC | 27 | a0001c0001t0001g0036 a0001c0001t0001g0067 a0001c0001t0001g0070 others(24): Show |
27 | HG01175.hp1 HG02071.hp1 HG02683.hp1 others(24): Show |
intron_variant | MODIFIER | c.732+4705_732+4706d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | |||||||
| chrX:136727395 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.732+4695_732+4706d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | |||||||
| chrX:136727395 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0012g0177 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.732+4706_732+4707i others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | |||||||
| chrX:136727397 | C | CTT | 13 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0144 others(10): Show |
13 | HG01981.hp1 HG02129.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.732+4704_732+4705i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727397 | |||||||
| chrX:136727399 | C | T | 7 | a0001c0001t0001g0164 a0001c0001t0001g0201 a0001c0001t0001g0216 others(4): Show |
7 | HG02970.hp2 NA18949.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+4703G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727399 | |||||||
| chrX:136727401 | C | T | 1 | a0006c0007t0001g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.732+4701G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727401 | |||||||
| chrX:136727411 | C | CTCTT | 6 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG00323.hp1 HG01081.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4687_732+4690d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | |||||||
| chrX:136727411 | C | CTT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(9): Show |
13 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.732+4690_732+4691i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | |||||||
| chrX:136727411 | C | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
69 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.732+4691G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | |||||||
| chrX:136727413 | CTT | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0219 a0001c0001t0003g0208 others(1): Show |
4 | HG01496.hp1 HG02970.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+4687_732+4688d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727413 | |||||||
| chrX:136727415 | T | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0036 others(98): Show |
101 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.732+4687A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727415 | |||||||
| chrX:136727418 | T | TC | 3 | a0001c0001t0001g0124 a0001c0001t0001g0175 a0001c0001t0003g0143 |
3 | NA18961.hp1 NA18980.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.732+4683_732+4684i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727418 | |||||||
| chrX:136727419 | T | C | 1 | a0001c0001t0005g0171 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.732+4683A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727419 | |||||||
| chrX:136727458 | CTTCT | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0087 others(1): Show |
4 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4640_732+4643d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727458 | |||||||
| chrX:136727466 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.732+4636A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727466 | |||||||
| chrX:136727503 | TCCTC | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | NA18986.hp1 NA19012.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4595_732+4598d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727503 | |||||||
| chrX:136727629 | G | C | 37 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
37 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.732+4473C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727629 | |||||||
| chrX:136727723 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0068 others(30): Show |
34 | HG00639.hp1 HG02055.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.732+4379C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727723 | |||||||
| chrX:136728759 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.732+3343C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136728759 | |||||||
| chrX:136728814 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0162 a0001c0001t0001g0188 others(1): Show |
4 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+3288C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136728814 | |||||||
| chrX:136728903 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.732+3199C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136728903 | |||||||
| chrX:136729000 | T | TTC | 10 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01175.hp2 HG03486.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+3100_732+3101d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | T | TTCTC | 5 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0045 others(2): Show |
5 | HG00639.hp2 HG00738.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+3098_732+3101d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | T | TTCTCTC | 6 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0069 others(3): Show |
6 | HG01192.hp1 HG01993.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+3096_732+3101d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | T | TTCTCTCT others(1): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0043 |
2 | HG03669.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.732+3094_732+3101d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTC | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0049 others(25): Show |
28 | HG00642.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.732+3100_732+3101d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTC | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0016 others(32): Show |
35 | HG01346.hp1 HG01928.hp1 HG02015.hp1 others(32): Show |
intron_variant | MODIFIER | c.732+3098_732+3101d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTC | T | 36 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(33): Show |
36 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.732+3096_732+3101d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(1): Show |
T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(50): Show |
53 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.732+3094_732+3101d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(3): Show |
T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
36 | HG00639.hp1 HG01515.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.732+3092_732+3101d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(5): Show |
T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0113 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG04199.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.732+3090_732+3101d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(7): Show |
T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0134 others(2): Show |
5 | HG00423.hp2 HG00621.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+3088_732+3101d others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(13): Show |
T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.732+3082_732+3101d others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729000 | TTCTCTCT others(19): Show |
T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+3076_732+3101d others(28): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729000 | |||||||
| chrX:136729051 | TCTC | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0197 a0001c0001t0003g0208 |
3 | HG01255.hp1 HG02004.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.732+3048_732+3050d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729051 | |||||||
| chrX:136729060 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.732+3042G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729060 | |||||||
| chrX:136729069 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.732+3033G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729069 | |||||||
| chrX:136729072 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.732+3030T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729072 | |||||||
| chrX:136729144 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.732+2958G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729144 | |||||||
| chrX:136729236 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(238): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.732+2866T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729236 | |||||||
| chrX:136729265 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.732+2837G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729265 | |||||||
| chrX:136729467 | C | CA | 15 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0040 others(12): Show |
15 | HG00438.hp2 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.732+2634dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729467 | |||||||
| chrX:136729467 | CA | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(39): Show |
43 | HG00423.hp1 HG00639.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.732+2634delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729467 | |||||||
| chrX:136729479 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.732+2623T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729479 | |||||||
| chrX:136729537 | G | T | 11 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0154 others(8): Show |
11 | HG00423.hp2 HG01934.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+2565C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729537 | |||||||
| chrX:136729541 | A | G | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.732+2561T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729541 | |||||||
| chrX:136729627 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.732+2475G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729627 | |||||||
| chrX:136729628 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0068 others(29): Show |
33 | HG00639.hp1 HG02055.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.732+2474C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729628 | |||||||
| chrX:136729699 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0087 others(1): Show |
4 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+2403C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729699 | |||||||
| chrX:136729723 | G | A | 2 | a0001c0001t0003g0243 a0001c0001t0003g0246 |
2 | HG00741.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.732+2379C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729723 | |||||||
| chrX:136729754 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+2348G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729754 | |||||||
| chrX:136729992 | A | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.732+2110T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729992 | |||||||
| chrX:136730023 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG00639.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+2079C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136730023 | |||||||
| chrX:136730081 | T | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.732+2021A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136730081 | |||||||
| chrX:136730806 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0113 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+1296A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136730806 | |||||||
| chrX:136730945 | A | G | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.732+1157T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136730945 | |||||||
| chrX:136731444 | A | T | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.732+658T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136731444 | |||||||
| chrX:136731606 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0068 others(30): Show |
34 | HG00639.hp1 HG02055.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.732+496T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136731606 | |||||||
| chrX:136732464 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.662-292G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136732464 | |||||||
| chrX:136732583 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.662-411C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136732583 | |||||||
| chrX:136732616 | G | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-444C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136732616 | |||||||
| chrX:136733129 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.662-957A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733129 | |||||||
| chrX:136733130 | T | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0121 a0001c0002t0002g0114 others(1): Show |
4 | HG00438.hp1 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-958A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733130 | |||||||
| chrX:136733254 | C | T | 2 | a0001c0001t0010g0117 a0001c0002t0001g0118 |
2 | HG01496.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.662-1082G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733254 | |||||||
| chrX:136733359 | T | C | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
46 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.662-1187A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733359 | |||||||
| chrX:136733546 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.662-1374G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733546 | |||||||
| chrX:136733697 | G | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-1525C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733697 | |||||||
| chrX:136733710 | C | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0080 others(1): Show |
4 | HG01074.hp1 HG01192.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1538G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733710 | |||||||
| chrX:136734105 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.662-1933C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734105 | |||||||
| chrX:136734247 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.662-2075G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734247 | |||||||
| chrX:136734248 | G | A | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.662-2076C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734248 | |||||||
| chrX:136734655 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-2483T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734655 | |||||||
| chrX:136734788 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-2616T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734788 | |||||||
| chrX:136735090 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.662-2918C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136735090 | |||||||
| chrX:136735979 | TAAG | T | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-3810_662-3808d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136735979 | |||||||
| chrX:136736154 | C | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-3982G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736154 | |||||||
| chrX:136736156 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-3984T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736156 | |||||||
| chrX:136736275 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0036 |
2 | NA18941.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.662-4103T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736275 | |||||||
| chrX:136736366 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.662-4194T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736366 | |||||||
| chrX:136736373 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.662-4201A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736373 | |||||||
| chrX:136736618 | G | GATGTGTG others(3): Show |
94 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0070 others(91): Show |
94 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.662-4447_662-4446i others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(5): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0244 a0001c0001t0002g0211 others(1): Show |
4 | HG02886.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4447_662-4446i others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(7): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0079 a0001c0001t0001g0093 others(15): Show |
18 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.662-4447_662-4446i others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(9): Show |
10 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG00639.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.662-4447_662-4446i others(18): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(11): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0010g0117 others(1): Show |
4 | HG01496.hp2 HG01891.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4447_662-4446i others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(13): Show |
1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.662-4447_662-4446i others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736618 | G | GATGTGTG others(15): Show |
2 | a0001c0001t0001g0104 a0001c0002t0002g0132 |
2 | HG02080.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.662-4447_662-4446i others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | |||||||
| chrX:136736619 | G | A | 2 | a0001c0001t0001g0147 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.662-4447C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736619 | |||||||
| chrX:136736621 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.662-4449C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736621 | |||||||
| chrX:136736630 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.662-4458A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736630 | |||||||
| chrX:136736650 | T | TG | 3 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0179 |
3 | HG03486.hp1 HG03486.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.662-4479_662-4478i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736650 | |||||||
| chrX:136736661 | C | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-4489G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736661 | |||||||
| chrX:136737177 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-5005A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737177 | |||||||
| chrX:136737298 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.662-5126A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737298 | |||||||
| chrX:136737382 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.662-5210T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737382 | |||||||
| chrX:136737442 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.662-5270C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737442 | |||||||
| chrX:136737545 | A | G | 1 | a0001c0001t0007g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-5373T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737545 | |||||||
| chrX:136737558 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.662-5386A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737558 | |||||||
| chrX:136737560 | C | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.662-5388G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737560 | |||||||
| chrX:136737582 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG00639.hp1 HG02080.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-5410C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737582 | |||||||
| chrX:136737683 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0002g0211 a0002c0004t0001g0130 others(1): Show |
4 | HG00438.hp1 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-5511C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737683 | |||||||
| chrX:136737687 | T | TA | 17 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0074 others(14): Show |
17 | HG00639.hp1 HG01981.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-5516dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737687 | |||||||
| chrX:136737687 | TA | T | 7 | a0001c0001t0001g0023 a0001c0001t0002g0003 a0001c0001t0002g0005 others(4): Show |
7 | HG01496.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-5516delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737687 | |||||||
| chrX:136737821 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.662-5649G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737821 | |||||||
| chrX:136738407 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.661+5178C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136738407 | |||||||
| chrX:136738419 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.661+5166T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136738419 | |||||||
| chrX:136738421 | T | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+5164A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136738421 | |||||||
| chrX:136738639 | G | A | 1 | a0003c0003t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661+4946C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136738639 | |||||||
| chrX:136740003 | C | CATT | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+3579_661+3581d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740003 | |||||||
| chrX:136740003 | C | CATTATT | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0003 others(4): Show |
7 | HG01496.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.661+3576_661+3581d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740003 | |||||||
| chrX:136740072 | G | A | 107 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0061 others(104): Show |
107 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.661+3513C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740072 | |||||||
| chrX:136740256 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.661+3329C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740256 | |||||||
| chrX:136740286 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.661+3299C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740286 | |||||||
| chrX:136740381 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(72): Show |
76 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.661+3204C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740381 | |||||||
| chrX:136740912 | T | G | 1 | a0001c0002t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.661+2673A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740912 | |||||||
| chrX:136741257 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.661+2328C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741257 | |||||||
| chrX:136741525 | C | CT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0063 others(2): Show |
5 | HG00423.hp2 HG01109.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+2059dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741525 | |||||||
| chrX:136741535 | T | TG | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0113 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+2049_661+2050i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741535 | |||||||
| chrX:136741537 | T | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(14): Show |
17 | HG01891.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.661+2048A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741537 | |||||||
| chrX:136741539 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.661+2046C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741539 | |||||||
| chrX:136742001 | G | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+1584C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742001 | |||||||
| chrX:136742095 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+1490G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742095 | |||||||
| chrX:136742103 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+1482T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742103 | |||||||
| chrX:136742188 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.661+1397T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742188 | |||||||
| chrX:136742235 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.661+1350G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742235 | |||||||
| chrX:136742263 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+1322T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742263 | |||||||
| chrX:136742287 | C | A | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0003 others(6): Show |
9 | HG01243.hp1 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+1298G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742287 | |||||||
| chrX:136742306 | A | G | 11 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0003 others(8): Show |
11 | HG01243.hp1 HG01496.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+1279T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742306 | |||||||
| chrX:136742332 | C | A | 1 | a0003c0003t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.661+1253G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742332 | |||||||
| chrX:136742335 | A | C | 1 | a0001c0001t0003g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.661+1250T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742335 | |||||||
| chrX:136742472 | C | T | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+1113G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742472 | |||||||
| chrX:136742581 | C | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
128 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.661+1004G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742581 | |||||||
| chrX:136742589 | T | C | 1 | a0001c0001t0005g0171 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.661+996A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742589 | |||||||
| chrX:136742838 | GA | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+746delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742838 | |||||||
| chrX:136742900 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.661+685C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742900 | |||||||
| chrX:136743231 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.661+354G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743231 | |||||||
| chrX:136743270 | GAGA | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(81): Show |
85 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+312_661+314del others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743270 | |||||||
| chrX:136743294 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.661+291T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743294 | |||||||
| chrX:136743314 | A | T | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.661+271T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743314 | |||||||
| chrX:136744263 | T | C | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.460-477A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744263 | |||||||
| chrX:136744363 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.460-577T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744363 | |||||||
| chrX:136744535 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+688A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744535 | |||||||
| chrX:136744687 | G | A | 1 | a0001c0001t0008g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459+536C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744687 | |||||||
| chrX:136744766 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+457A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744766 | |||||||
| chrX:136745027 | C | T | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.459+196G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136745027 | |||||||
| chrX:136745065 | T | C | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.459+158A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136745065 | |||||||
| chrX:136745069 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+154C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136745069 | |||||||
| chrX:136745150 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.459+73A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136745150 | |||||||
| chrX:136745481 | C | T | 1 | a0001c0001t0006g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.335-134G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136745481 | |||||||
| chrX:136745739 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.335-392G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136745739 | |||||||
| chrX:136745751 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | NA18945.hp1 NA18955.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.335-404A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136745751 | |||||||
| chrX:136745871 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.335-524A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136745871 | |||||||
| chrX:136746082 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.335-735T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136746082 | |||||||
| chrX:136746133 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
6 | HG00639.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-786C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136746133 | |||||||
| chrX:136747218 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.334+290A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 3/21 | chrX | 136747218 | |||||||
| chrX:136747617 | G | A | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-25C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747617 | |||||||
| chrX:136747670 | C | T | 1 | a0001c0001t0004g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-78G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747670 | |||||||
| chrX:136747682 | C | CA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0047 others(24): Show |
28 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-91_250-90insT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747682 | |||||||
| chrX:136747683 | G | A | 53 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(50): Show |
53 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.250-91C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747683 | |||||||
| chrX:136747684 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0047 others(24): Show |
28 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-92C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747684 | |||||||
| chrX:136747684 | G | GA | 10 | a0001c0001t0001g0078 a0001c0001t0001g0103 a0001c0001t0001g0124 others(7): Show |
10 | HG00621.hp1 HG02145.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.250-93dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747684 | |||||||
| chrX:136747684 | G | GAA | 6 | a0001c0001t0002g0005 a0001c0001t0010g0117 a0001c0002t0001g0118 others(3): Show |
6 | HG01496.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-94_250-93dupTT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747684 | |||||||
| chrX:136747684 | GA | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0080 a0001c0001t0001g0151 others(3): Show |
6 | HG02886.hp1 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-93delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747684 | |||||||
| chrX:136747712 | A | G | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-120T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747712 | |||||||
| chrX:136747751 | G | A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0005g0148 others(4): Show |
7 | HG02129.hp1 NA18612.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-159C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747751 | |||||||
| chrX:136747762 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-170A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747762 | |||||||
| chrX:136747980 | G | A | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-388C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136747980 | |||||||
| chrX:136748160 | C | T | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-568G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748160 | |||||||
| chrX:136748193 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-601A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748193 | |||||||
| chrX:136748271 | C | T | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-679G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748271 | |||||||
| chrX:136748331 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-739C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748331 | |||||||
| chrX:136748532 | A | G | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-940T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748532 | |||||||
| chrX:136748782 | C | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-1190G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748782 | |||||||
| chrX:136748807 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.250-1215A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748807 | |||||||
| chrX:136748816 | G | A | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-1224C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748816 | |||||||
| chrX:136748913 | G | A | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-1321C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136748913 | |||||||
| chrX:136749118 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.250-1526T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136749118 | |||||||
| chrX:136749202 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.250-1610A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136749202 | |||||||
| chrX:136749203 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.250-1611C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136749203 | |||||||
| chrX:136749257 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0240 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.250-1665G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136749257 | |||||||
| chrX:136749349 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.250-1757T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136749349 | |||||||
| chrX:136750058 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(77): Show |
81 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.250-2466C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750058 | |||||||
| chrX:136750190 | A | C | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-2598T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750190 | |||||||
| chrX:136750607 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-3015A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750607 | |||||||
| chrX:136750804 | C | CT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0120 others(4): Show |
7 | HG01993.hp1 NA18945.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-3213dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750804 | |||||||
| chrX:136750804 | CT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.250-3213delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750804 | |||||||
| chrX:136750842 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.250-3250G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750842 | |||||||
| chrX:136750888 | C | T | 11 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG00639.hp1 HG02080.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-3296G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750888 | |||||||
| chrX:136751089 | A | G | 2 | a0002c0004t0001g0130 a0002c0004t0009g0174 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.250-3497T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751089 | |||||||
| chrX:136751128 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.250-3536G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751128 | |||||||
| chrX:136751272 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0080 others(1): Show |
4 | HG01074.hp1 HG01192.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-3680T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751272 | |||||||
| chrX:136751483 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.250-3891G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751483 | |||||||
| chrX:136751648 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.250-4056G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751648 | |||||||
| chrX:136752031 | A | G | 2 | a0001c0001t0007g0119 a0001c0001t0007g0194 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.250-4439T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752031 | |||||||
| chrX:136752047 | T | C | 3 | a0001c0001t0002g0211 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.250-4455A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752047 | |||||||
| chrX:136752202 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0149 |
2 | HG00673.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.250-4610A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752202 | |||||||
| chrX:136752257 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.250-4665G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752257 | |||||||
| chrX:136752337 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.250-4745T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752337 | |||||||
| chrX:136752379 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.250-4787G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752379 | |||||||
| chrX:136752463 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-4871A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752463 | |||||||
| chrX:136752549 | C | T | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-4957G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752549 | |||||||
| chrX:136752735 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-5143C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752735 | |||||||
| chrX:136752763 | C | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-5171G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752763 | |||||||
| chrX:136752881 | T | C | 3 | a0001c0001t0001g0244 a0002c0004t0001g0130 a0002c0004t0009g0174 |
3 | HG02451.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.250-5289A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752881 | |||||||
| chrX:136752931 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-5339C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752931 | |||||||
| chrX:136753003 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-5411C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753003 | |||||||
| chrX:136753161 | G | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-5569C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753161 | |||||||
| chrX:136753215 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-5623G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753215 | |||||||
| chrX:136753286 | C | T | 11 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG00639.hp1 HG02080.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-5694G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753286 | |||||||
| chrX:136753313 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.250-5721A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753313 | |||||||
| chrX:136753587 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.250-5995G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753587 | |||||||
| chrX:136753625 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(200): Show |
204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.250-6033A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753625 | |||||||
| chrX:136753792 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
206 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.250-6200G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753792 | |||||||
| chrX:136753952 | G | C | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-6360C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753952 | |||||||
| chrX:136754051 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.250-6459T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754051 | |||||||
| chrX:136754160 | G | C | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.250-6568C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754160 | |||||||
| chrX:136754256 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(190): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.250-6664C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754256 | |||||||
| chrX:136754362 | G | A | 1 | a0001c0001t0005g0171 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.250-6770C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754362 | |||||||
| chrX:136754524 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.250-6932C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754524 | |||||||
| chrX:136754595 | AAC | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.250-7005_250-7004d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754595 | |||||||
| chrX:136754596 | AC | A | 23 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0053 others(20): Show |
23 | HG00140.hp1 HG00438.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-7005delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754596 | |||||||
| chrX:136754597 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0113 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-7005G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754597 | |||||||
| chrX:136754793 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0109 a0001c0001t0002g0212 |
3 | HG01243.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.250-7201C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754793 | |||||||
| chrX:136755060 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.250-7468G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755060 | |||||||
| chrX:136755417 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-7825A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755417 | |||||||
| chrX:136755588 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.250-7996C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755588 | |||||||
| chrX:136755619 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
207 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.250-8027G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755619 | |||||||
| chrX:136755671 | C | T | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-8079G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755671 | |||||||
| chrX:136755719 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0013g0031 |
3 | HG01071.hp2 HG01099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.250-8127A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755719 | |||||||
| chrX:136755801 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-8209A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755801 | |||||||
| chrX:136756031 | C | T | 1 | a0001c0001t0008g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.250-8439G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756031 | |||||||
| chrX:136756296 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-8704A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756296 | |||||||
| chrX:136756317 | T | C | 8 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-8725A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756317 | |||||||
| chrX:136756380 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.250-8788T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756380 | |||||||
| chrX:136756696 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-9104A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756696 | |||||||
| chrX:136756730 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.250-9138C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136756730 | |||||||
| chrX:136757169 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.250-9577G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757169 | |||||||
| chrX:136757220 | T | C | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-9628A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757220 | |||||||
| chrX:136757418 | A | C | 2 | a0001c0001t0001g0113 a0001c0002t0002g0128 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-9826T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757418 | |||||||
| chrX:136757526 | C | T | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.250-9934G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757526 | |||||||
| chrX:136757543 | A | G | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-9951T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757543 | |||||||
| chrX:136757840 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.250-10248C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136757840 | |||||||
| chrX:136758026 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250-10434T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758026 | |||||||
| chrX:136758031 | C | CT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01168.hp1 HG02145.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-10440dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0021 others(20): Show |
23 | HG00642.hp1 HG01099.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.250-10441_250-1044 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTT | 58 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0033 others(55): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.250-10442_250-1044 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTT | 52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0047 others(49): Show |
52 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.250-10443_250-1044 others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTTT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(35): Show |
39 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.250-10444_250-1044 others(9): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTTTT | 21 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0052 others(18): Show |
21 | HG00438.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-10445_250-1044 others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTTTTT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0077 others(4): Show |
7 | HG01243.hp1 HG02074.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-10446_250-1044 others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0101 a0001c0001t0001g0106 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-10449_250-1044 others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0053 |
2 | HG01261.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.250-10450_250-1044 others(15): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.250-10449_250-1044 others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | CTTTTTTT others(4): Show |
C | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-10450_250-1044 others(15): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0063 a0003c0003t0001g0182 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.250-10452_250-1044 others(17): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758031 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.250-10456_250-1044 others(21): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | |||||||
| chrX:136758070 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.250-10478C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758070 | |||||||
| chrX:136758280 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.250-10688A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758280 | |||||||
| chrX:136758366 | T | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG00639.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-10774A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758366 | |||||||
| chrX:136758506 | G | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.250-10914C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758506 | |||||||
| chrX:136758766 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0220 others(27): Show |
31 | HG00423.hp1 HG00741.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.250-11174G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758766 | |||||||
| chrX:136758882 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.250-11290A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758882 | |||||||
| chrX:136759236 | A | T | 1 | a0001c0001t0005g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-11644T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759236 | |||||||
| chrX:136759274 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.250-11682A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759274 | |||||||
| chrX:136759351 | C | A | 1 | a0001c0001t0003g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.250-11759G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759351 | |||||||
| chrX:136759452 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0004g0223 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.250-11860G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759452 | |||||||
| chrX:136759627 | C | CA | 17 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(14): Show |
17 | HG01496.hp2 HG01891.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.250-12036dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759627 | |||||||
| chrX:136759829 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250-12237G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759829 | |||||||
| chrX:136759912 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-12320A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759912 | |||||||
| chrX:136760534 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-12942G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136760534 | |||||||
| chrX:136760712 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.250-13120T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136760712 | |||||||
| chrX:136760864 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0219 others(28): Show |
32 | HG00423.hp1 HG00741.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.250-13272A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136760864 | |||||||
| chrX:136760923 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.250-13331C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136760923 | |||||||
| chrX:136761721 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
197 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.250-14129G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761721 | |||||||
| chrX:136761763 | G | A | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0002g0003 others(6): Show |
9 | HG01496.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-14171C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761763 | |||||||
| chrX:136761844 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-14252T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761844 | |||||||
| chrX:136761912 | CT | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0172 others(2): Show |
5 | HG01891.hp2 HG02027.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-14321delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761912 | |||||||
| chrX:136761913 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-14321A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761913 | |||||||
| chrX:136762326 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.250-14734A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762326 | |||||||
| chrX:136762504 | T | C | 1 | a0001c0001t0005g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14912A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762504 | |||||||
| chrX:136762772 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-15180C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762772 | |||||||
| chrX:136762969 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.250-15377C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762969 | |||||||
| chrX:136763346 | C | T | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-15754G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763346 | |||||||
| chrX:136763401 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-15809G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763401 | |||||||
| chrX:136763546 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.249+15868G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763546 | |||||||
| chrX:136763682 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.249+15732C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763682 | |||||||
| chrX:136763870 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.249+15544A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763870 | |||||||
| chrX:136764103 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.249+15311G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764103 | |||||||
| chrX:136764122 | ATGGTTCT others(6): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.249+15279_249+1529 others(17): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764122 | |||||||
| chrX:136764168 | C | CA | 6 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0036 others(3): Show |
6 | HG01515.hp1 HG03195.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+15245dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764168 | |||||||
| chrX:136764221 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.249+15193G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764221 | |||||||
| chrX:136764342 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0002t0002g0114 |
3 | HG02818.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.249+15072A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764342 | |||||||
| chrX:136764345 | TTCACAGC others(31): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.249+15031_249+1506 others(42): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764345 | |||||||
| chrX:136764387 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.249+15027T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764387 | |||||||
| chrX:136764585 | G | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0002t0002g0114 |
3 | HG02818.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.249+14829C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764585 | |||||||
| chrX:136764596 | C | T | 1 | a0001c0002t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+14818G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764596 | |||||||
| chrX:136764827 | A | T | 1 | a0001c0001t0001g0006 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.249+14587T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764827 | |||||||
| chrX:136764845 | C | T | 112 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0099 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.249+14569G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764845 | |||||||
| chrX:136764939 | A | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(33): Show |
37 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+14475T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764939 | |||||||
| chrX:136765214 | T | C | 94 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0120 others(91): Show |
94 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.249+14200A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765214 | |||||||
| chrX:136765310 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.249+14104T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765310 | |||||||
| chrX:136765524 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.249+13890G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765524 | |||||||
| chrX:136765541 | G | T | 1 | a0002c0004t0001g0130 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+13873C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765541 | |||||||
| chrX:136765572 | A | C | 1 | a0005c0005t0001g0092 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.249+13842T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765572 | |||||||
| chrX:136765648 | C | A | 112 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0099 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.249+13766G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765648 | |||||||
| chrX:136765677 | T | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+13737A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765677 | |||||||
| chrX:136765731 | A | G | 1 | a0003c0003t0002g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+13683T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765731 | |||||||
| chrX:136765961 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.249+13453G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136765961 | |||||||
| chrX:136766148 | A | AT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+13265dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766148 | |||||||
| chrX:136766294 | T | TA | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.249+13119dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766294 | |||||||
| chrX:136766381 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.249+13033C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766381 | |||||||
| chrX:136766392 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249+13022A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766392 | |||||||
| chrX:136766392 | T | TG | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.249+13021dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766392 | |||||||
| chrX:136766392 | T | TTG | 5 | a0001c0001t0001g0052 a0001c0001t0001g0181 a0001c0001t0001g0187 others(2): Show |
5 | HG01496.hp1 HG03239.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+13021_249+1302 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766392 | |||||||
| chrX:136766957 | C | G | 9 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+12457G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766957 | |||||||
| chrX:136767239 | G | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.249+12175C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767239 | |||||||
| chrX:136767246 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.249+12168G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767246 | |||||||
| chrX:136767337 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0219 others(29): Show |
33 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.249+12077G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767337 | |||||||
| chrX:136767414 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG00323.hp1 HG00642.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+12000C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767414 | |||||||
| chrX:136767423 | C | G | 56 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(53): Show |
56 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.249+11991G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767423 | |||||||
| chrX:136767475 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.249+11939A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767475 | |||||||
| chrX:136767710 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.249+11704G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767710 | |||||||
| chrX:136767731 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.249+11683C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767731 | |||||||
| chrX:136767838 | GAGC | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
95 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.249+11573_249+1157 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767838 | |||||||
| chrX:136767838 | GAGCAGCA others(5): Show |
G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0121 others(98): Show |
101 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.249+11564_249+1157 others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767838 | |||||||
| chrX:136767960 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.249+11454C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767960 | |||||||
| chrX:136768005 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0181 a0001c0001t0001g0184 |
3 | NA18962.hp1 NA18965.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.249+11409G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136768005 | |||||||
| chrX:136768125 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.249+11289A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136768125 | |||||||
| chrX:136768369 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.249+11045G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136768369 | |||||||
| chrX:136768619 | G | A | 1 | a0002c0004t0009g0174 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.249+10795C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136768619 | |||||||
| chrX:136769081 | C | T | 1 | a0001c0001t0008g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249+10333G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769081 | |||||||
| chrX:136769210 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.249+10204C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769210 | |||||||
| chrX:136769268 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(238): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.249+10146C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769268 | |||||||
| chrX:136769653 | G | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0207 others(1): Show |
4 | NA18952.hp1 NA18968.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+9761C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769653 | |||||||
| chrX:136769707 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+9707T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769707 | |||||||
| chrX:136769764 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.249+9650T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769764 | |||||||
| chrX:136770193 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.249+9221A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770193 | |||||||
| chrX:136770234 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.249+9180T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770234 | |||||||
| chrX:136770246 | A | G | 1 | a0001c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.249+9168T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770246 | |||||||
| chrX:136770252 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0207 others(1): Show |
4 | NA18952.hp1 NA18968.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+9162A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770252 | |||||||
| chrX:136770631 | T | C | 1 | a0001c0001t0005g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+8783A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770631 | |||||||
| chrX:136770638 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.249+8776G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770638 | |||||||
| chrX:136770751 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.249+8663A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770751 | |||||||
| chrX:136771221 | C | T | 1 | a0001c0001t0004g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.249+8193G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136771221 | |||||||
| chrX:136771424 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.249+7990G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136771424 | |||||||
| chrX:136771782 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.249+7632T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136771782 | |||||||
| chrX:136771814 | C | T | 102 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0121 others(99): Show |
102 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.249+7600G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136771814 | |||||||
| chrX:136772299 | G | A | 1 | a0003c0003t0002g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+7115C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136772299 | |||||||
| chrX:136772351 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0219 others(29): Show |
33 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.249+7063A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136772351 | |||||||
| chrX:136772581 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.249+6833A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136772581 | |||||||
| chrX:136772608 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.249+6806G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136772608 | |||||||
| chrX:136772691 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.249+6723C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136772691 | |||||||
| chrX:136773143 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.249+6271C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773143 | |||||||
| chrX:136773147 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+6267G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773147 | |||||||
| chrX:136773253 | C | A | 1 | a0001c0001t0001g0036 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.249+6161G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773253 | |||||||
| chrX:136773335 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.249+6079C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773335 | |||||||
| chrX:136773400 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0093 |
2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.249+6014A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773400 | |||||||
| chrX:136773439 | G | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+5975C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773439 | |||||||
| chrX:136773642 | G | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(37): Show |
40 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.249+5772C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773642 | |||||||
| chrX:136773678 | T | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | HG02818.hp1 HG03540.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+5736A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773678 | |||||||
| chrX:136773754 | T | C | 1 | a0001c0001t0003g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.249+5660A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773754 | |||||||
| chrX:136773885 | T | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+5529A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136773885 | |||||||
| chrX:136774131 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.249+5283A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774131 | |||||||
| chrX:136774328 | TCAC | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.249+5083_249+5085d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774328 | |||||||
| chrX:136774650 | C | CA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0113 a0001c0001t0001g0181 others(26): Show |
30 | HG00423.hp1 HG00741.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+4763dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774650 | |||||||
| chrX:136774650 | CA | C | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.249+4763delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774650 | |||||||
| chrX:136775196 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0002t0002g0114 |
3 | HG02818.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.249+4218A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775196 | |||||||
| chrX:136775266 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.249+4148G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775266 | |||||||
| chrX:136775298 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.249+4116G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775298 | |||||||
| chrX:136775602 | G | C | 1 | a0003c0003t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.249+3812C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775602 | |||||||
| chrX:136775690 | T | C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
44 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.249+3724A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775690 | |||||||
| chrX:136776138 | G | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
44 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.249+3276C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776138 | |||||||
| chrX:136776259 | C | G | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.249+3155G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776259 | |||||||
| chrX:136776524 | G | A | 1 | a0005c0005t0001g0092 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.249+2890C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776524 | |||||||
| chrX:136776616 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.249+2798G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776616 | |||||||
| chrX:136776736 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18949.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.249+2678G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776736 | |||||||
| chrX:136776878 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.249+2536C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776878 | |||||||
| chrX:136776878 | G | GATAA | 63 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.249+2532_249+2535d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776878 | |||||||
| chrX:136776878 | G | GATAAATA others(1): Show |
8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0044 others(5): Show |
8 | HG00639.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+2528_249+2535d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776878 | |||||||
| chrX:136776878 | GATAA | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
11 | HG01496.hp2 HG02071.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+2532_249+2535d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776878 | |||||||
| chrX:136776878 | GATAAATA others(1): Show |
G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(39): Show |
43 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.249+2528_249+2535d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776878 | |||||||
| chrX:136776894 | A | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0113 others(33): Show |
37 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+2520T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776894 | |||||||
| chrX:136776947 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.249+2467C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776947 | |||||||
| chrX:136776999 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.249+2415G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776999 | |||||||
| chrX:136777000 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.249+2414C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777000 | |||||||
| chrX:136777200 | G | C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
44 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.249+2214C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777200 | |||||||
| chrX:136777273 | G | A | 1 | a0001c0001t0003g0208 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.249+2141C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777273 | |||||||
| chrX:136777422 | T | TA | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.249+1991dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777422 | |||||||
| chrX:136777597 | T | C | 57 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
57 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.249+1817A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777597 | |||||||
| chrX:136777761 | T | TAC | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0002g0211 |
3 | HG02027.hp1 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.249+1651_249+1652d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(1): Show |
6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02074.hp1 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+1645_249+1652d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(3): Show |
35 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(32): Show |
35 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.249+1643_249+1652d others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(5): Show |
48 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0049 others(45): Show |
48 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.249+1641_249+1652d others(14): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0004g0096 others(1): Show |
4 | HG02148.hp1 HG03710.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+1639_249+1652d others(16): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.249+1637_249+1652d others(18): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(11): Show |
6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG02080.hp1 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+1635_249+1652d others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(13): Show |
4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1633_249+1652d others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136777761 | T | TACACACA others(15): Show |
2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.249+1631_249+1652d others(24): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777761 | |||||||
| chrX:136778159 | G | T | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.249+1255C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778159 | |||||||
| chrX:136778166 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.249+1248C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778166 | |||||||
| chrX:136778218 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | NA18986.hp1 NA19012.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.249+1196A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778218 | |||||||
| chrX:136778310 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | NA18939.hp1 NA18964.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+1104T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778310 | |||||||
| chrX:136778504 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0219 others(27): Show |
31 | HG00423.hp1 HG00741.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.249+910G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778504 | |||||||
| chrX:136778676 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18949.hp1 NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.249+738C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778676 | |||||||
| chrX:136779553 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-56A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136779553 | |||||||
| chrX:136779686 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.166-189T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136779686 | |||||||
| chrX:136780523 | G | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+195C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136780523 | |||||||
| chrX:136780568 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0219 a0001c0001t0001g0220 others(26): Show |
30 | HG00423.hp1 HG00741.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+150A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136780568 |