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 | 239 | 64 | 45 | 98 | 7 | 23 | 75 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0002 | 0/0 | 776 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0003 | 0/0 | 776 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0004 | 0/0 | 776 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0005 | 0/0 | 776 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0006 | 0/0 | 479 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0007 | 0/0 | 756 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2331 | 234 | 60 | 45 | 98 | 7 | 22 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0002 | 0/0 | 2331 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0003 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0004 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0005 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0006 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0007 | 0/0 | 2330 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0008 | 0/0 | 2336 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
c0009 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2530 | 206 | 55 | 38 | 86 | 6 | 19 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0002 | 0/0 | 2530 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0003 | 0/0 | 2530 | 6 | 0 | 2 | 4 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0004 | 0/0 | 2530 | 5 | 2 | 1 | 1 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0005 | 0/0 | 2530 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0006 | 0/0 | 2530 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0007 | 0/0 | 2530 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0008 | 0/0 | 2530 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0009 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0010 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0011 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0012 | 0/0 | 2531 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0013 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0014 | 0/0 | 2530 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0015 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0016 | 0/0 | 2530 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0017 | 0/0 | 2530 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0018 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0019 | 0/0 | 2530 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
t0020 | 0/0 | 2530 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2331 | 234 | 60 | 45 | 98 | 7 | 22 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0001c0002 | 0/0 | 2331 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0001c0006 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0002c0004 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0003c0003 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0004c0005 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0005c0009 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0006c0008 | 0/0 | 2336 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 | |
a0007c0007 | 0/0 | 2330 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4860 | 200 | 52 | 38 | 84 | 6 | 18 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0002 | 0/0 | 4860 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0003 | 0/0 | 4860 | 6 | 0 | 2 | 4 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0004 | 0/0 | 4860 | 5 | 2 | 1 | 1 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0005 | 0/0 | 4860 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0006 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0007 | 0/0 | 4860 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0008 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0009 | 0/0 | 4856 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0011 | 0/0 | 4855 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0012 | 0/0 | 4861 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0014 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0015 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0016 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0017 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0018 | 0/0 | 4859 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0019 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0001t0020 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0002t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0002t0002 | 0/0 | 4860 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0001c0006t0001 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0002c0004t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0002c0004t0013 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0003c0003t0001 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0003c0003t0002 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0004c0005t0001 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0005c0009t0006 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0006c0008t0001 | 0/0 | 4865 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | chrX | 136660550 | 136785932 |
a0007c0007t0010 | 0/0 | 4858 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | copy fasta | 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 |
a0001c0001t0001g0003 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0085 | 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 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0092 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0114 | 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 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0148 | 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 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0156 | 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 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0179 | 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 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 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 | 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 |
a0001c0001t0001g0243 | 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 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0002g0004 | 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 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0004g0042 | 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 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0007g0190 | 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 |
a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0011g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0014g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0015g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0016g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0017g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0018g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0019g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0001c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0002c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0002c0004t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0003c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0004c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0005c0009t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0006c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
a0007c0007t0010g0021 | 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 | g0194 | EUR | GBR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0185 | 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 | t0018 | 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 | g0044 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0091 | 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 | g0048 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01346 | hp2 | a0001 | c0001 | t0016 | g0034 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01496 | hp2 | a0001 | c0001 | t0014 | g0116 | AMR | CLM | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0195 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0120 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0104 | 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 | g0129 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0036 | 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 | g0206 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02451 | hp1 | a0002 | c0004 | t0013 | g0172 | 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 | g0075 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0082 | 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 | g0171 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0005 | 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 | g0223 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0072 | 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 | g0092 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02809 | hp2 | a0002 | c0004 | t0001 | g0128 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0221 | 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 | g0103 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | 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 | g0228 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0064 | 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 | a0005 | c0009 | t0006 | g0086 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0240 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03688 | hp1 | a0001 | c0006 | t0001 | g0041 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0067 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03942 | hp1 | a0001 | c0001 | t0020 | g0098 | SAS | BEB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG04228 | hp1 | a0001 | c0001 | t0017 | g0188 | SAS | STU | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18949 | hp2 | a0001 | c0001 | t0019 | g0134 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0169 | 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 | g0023 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18980 | hp1 | a0004 | c0005 | t0001 | g0093 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19058 | hp1 | a0001 | c0001 | t0011 | g0174 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19075 | hp1 | a0007 | c0007 | t0010 | g0021 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19076 | hp1 | a0006 | c0008 | t0001 | g0124 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0224 | AFR | ASW | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0042 | EUR | TSI | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | GIH | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0226 | 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 | g0212 | 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 | g0095 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | LWK | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | ARHGEF6_chrX_136660550_136785932 | ARHGEF6 | chrX | 136660550 | 136785932 |
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:136668089 | CA | C | 1 | a0007 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.2270delT | p.Leu757fs | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2320/4860 | 2270/2331 | 757/776 | chrX | 136668089 | ||
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:136682831 | C | CCGCCT | 1 | a0006 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1405_1406insAGGCG | p.Arg469fs | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/22 | 1455/4860 | 1405/2331 | 469/776 | chrX | 136682831 | ||
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 | a0005 | 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 | a0004 | 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 |
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 |
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 | a0001c0001t0016 | 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:136665596 | TA | T | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2432delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2432 | chrX | 136665596 | |||||
chrX:136665620 | GT | G | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2408delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2408 | chrX | 136665620 | |||||
chrX:136665627 | A | T | 1 | a0001c0001t0011 | 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 | a0001c0001t0006a0005c0009t0006 | 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:136665727 | T | TA | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2301dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 2301 | chrX | 136665727 | |||||
chrX:136665881 | C | T | 1 | a0001c0001t0015 | 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 | a0001c0001t0014 | 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 | a0001c0001t0017 | 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:136666059 | TG | T | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1969delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1969 | chrX | 136666059 | |||||
chrX:136666103 | T | TTA | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1924_*1925dupTA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1925 | chrX | 136666103 | |||||
chrX:136666153 | AT | A | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1875delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1875 | chrX | 136666153 | |||||
chrX:136666211 | CA | C | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1817delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1817 | chrX | 136666211 | |||||
chrX:136666349 | C | CA | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1679 | chrX | 136666349 | |||||
chrX:136666352 | A | T | 1 | a0002c0004t0013 | 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:136666380 | A | AG | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1648dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1648 | chrX | 136666380 | |||||
chrX:136666497 | AG | A | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1531 | chrX | 136666497 | |||||
chrX:136666530 | GT | G | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1498 | chrX | 136666530 | |||||
chrX:136666617 | A | AT | 1 | a0001c0001t0012 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1411 | chrX | 136666617 | |||||
chrX:136666617 | AT | A | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1411 | chrX | 136666617 | |||||
chrX:136666679 | T | TG | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1349 | chrX | 136666679 | |||||
chrX:136666688 | GC | G | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1340 | chrX | 136666688 | |||||
chrX:136666716 | AT | A | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1312delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1312 | chrX | 136666716 | |||||
chrX:136666777 | TG | T | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1251 | chrX | 136666777 | |||||
chrX:136666806 | A | AG | 1 | a0001c0001t0011 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1222 | chrX | 136666806 | |||||
chrX:136666886 | AC | A | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 1142 | chrX | 136666886 | |||||
chrX:136666888 | C | A | 3 | a0001c0001t0002a0001c0002t0002a0003c0003t0002 | 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:136667100 | AT | A | 1 | a0001c0001t0018 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 928 | chrX | 136667100 | |||||
chrX:136667389 | T | C | 1 | a0001c0001t0019 | 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:136667569 | TG | T | 1 | a0007c0007t0010 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 459 | chrX | 136667569 | |||||
chrX:136667779 | T | C | 1 | a0001c0001t0020 | 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:136667894 | GAAGA | G | 1 | a0001c0001t0009 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131_*134delTCTT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 22/22 | 131 | chrX | 136667894 | |||||
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 |
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 | a0001c0001t0019g0134 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(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 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0052others(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 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0112others(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 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0003g0142others(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:136668521 | C | CTTATTA | 1 | a0001c0001t0001g0023 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2191-353_2191-352i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668521 | ||||||
chrX:136668524 | C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0023 | 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 | a0001c0001t0001g0016a0001c0001t0001g0023 | 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:136668527 | C | CTTA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2191-359_2191-358i others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668527 | ||||||
chrX:136668527 | C | CTTATTA | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2191-359_2191-358i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668527 | ||||||
chrX:136668530 | C | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(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:136668530 | C | CTTATTA | 1 | a0001c0001t0001g0012 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2191-362_2191-361i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668530 | ||||||
chrX:136668533 | C | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(40): Show | 43 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(40): 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 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0071others(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 | a0001c0001t0001g0055a0001c0001t0001g0218a0001c0001t0001g0228others(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 | a0001c0001t0001g0025a0001c0001t0001g0056a0001c0001t0001g0168others(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 | C | CTTCTTAT others(2): Show |
1 | a0002c0004t0013g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2191-365_2191-364i others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | ||||||
chrX:136668533 | C | CTTCTTCT others(2): Show |
1 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2191-365_2191-364i others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | ||||||
chrX:136668533 | CTTA | C | 25 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0089others(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 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0112others(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:136668533 | CTTATTAT others(2): Show |
C | 1 | a0001c0001t0003g0246 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2191-373_2191-365d others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668533 | ||||||
chrX:136668536 | A | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0026others(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 | a0001c0001t0001g0036a0001c0001t0001g0063a0001c0001t0001g0069others(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 | a0001c0001t0001g0063a0001c0001t0001g0114a0001c0001t0001g0115others(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:136668554 | ATTATT | A | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2191-390_2191-386d others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668554 | ||||||
chrX:136668675 | T | C | 2 | a0001c0002t0002g0171a0003c0003t0002g0212 | 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:136668719 | TA | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2191-551delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136668719 | ||||||
chrX:136669004 | T | C | 1 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0137a0001c0001t0001g0200 | 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 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2190+219A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136669263 | ||||||
chrX:136669431 | GA | G | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2190+50delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | 136669431 | ||||||
chrX:136669770 | CCCT | C | 1 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2136-237_2136-235d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 20/21 | chrX | 136669770 | ||||||
chrX:136669793 | C | T | 1 | a0001c0001t0001g0225 | 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 | a0001c0001t0009g0064 | 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 | a0001c0001t0017g0188 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0194others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0013a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0242a0001c0001t0014g0116 | 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 | a0001c0001t0014g0116 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136674919 | TC | T | 1 | a0001c0001t0001g0140 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2035+87delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 19/21 | chrX | 136674919 | ||||||
chrX:136674920 | C | G | 1 | a0001c0001t0001g0045 | 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 | a0001c0002t0002g0171 | 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 | a0001c0001t0001g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1946-130G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675226 | ||||||
chrX:136675350 | T | TG | 5 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0051others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1946-255dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 18/21 | chrX | 136675350 | ||||||
chrX:136675356 | G | A | 1 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0026others(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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0016g0034 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0014g0116 | 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 | a0001c0002t0001g0117a0001c0002t0002g0113a0001c0002t0002g0130others(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 | a0006c0008t0001g0124 | 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 | a0001c0001t0004g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1851+455T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677481 | ||||||
chrX:136677839 | AG | A | 1 | a0001c0001t0001g0210 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1851+96delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 17/21 | chrX | 136677839 | ||||||
chrX:136677860 | G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005 | 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 | a0001c0001t0004g0042a0001c0001t0004g0096a0001c0001t0004g0111 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0009g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1830+740A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678795 | ||||||
chrX:136678915 | TGA | T | 1 | a0001c0001t0012g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1830+618_1830+619d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136678915 | ||||||
chrX:136679395 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+140T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136679395 | ||||||
chrX:136679513 | A | AT | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1830+21dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 16/21 | chrX | 136679513 | ||||||
chrX:136679869 | A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0009g0064 | 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 | a0001c0001t0019g0134 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0028 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1559-353G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681229 | ||||||
chrX:136681469 | ATTTG | A | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1558+417_1558+420d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 14/21 | chrX | 136681469 | ||||||
chrX:136681563 | G | C | 1 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005 | 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 | a0001c0001t0005g0150a0001c0001t0005g0151 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1479+254A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682504 | ||||||
chrX:136682702 | TG | T | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1479+55delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 13/21 | chrX | 136682702 | ||||||
chrX:136682716 | C | T | 1 | a0001c0001t0001g0186 | 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 | a0001c0001t0017g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1393-84T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682928 | ||||||
chrX:136682964 | AT | A | 1 | a0001c0001t0001g0192 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1393-121delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682964 | ||||||
chrX:136682974 | T | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0075a0001c0001t0001g0126 | 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:136682974 | TA | T | 1 | a0001c0001t0011g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1393-131delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136682974 | ||||||
chrX:136682975 | A | T | 1 | a0001c0001t0001g0044 | 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 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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:136683398 | GC | G | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1393-555delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683398 | ||||||
chrX:136683427 | C | T | 1 | a0001c0001t0004g0229 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136683623 | CT | C | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1393-780delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683623 | ||||||
chrX:136683701 | C | CA | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1393-858dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683701 | ||||||
chrX:136683911 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1393-1067C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683911 | ||||||
chrX:136683914 | CCT | C | 1 | a0001c0001t0001g0015 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1393-1072_1393-107 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136683914 | ||||||
chrX:136684097 | A | T | 1 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0082 | 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 | a0001c0002t0002g0130 | 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 | a0001c0001t0014g0116 | 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 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0011a0001c0001t0001g0100a0001c0001t0001g0101others(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 | C | CAA | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0002c0004t0001g0128 | 3 | HG01891.hp2 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1392+71_1392+72dup others(2): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685604 | ||||||
chrX:136685604 | CA | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0025a0001c0001t0001g0037others(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:136685604 | CAAAAAAA | C | 2 | a0001c0001t0001g0012a0001c0001t0017g0188 | 2 | HG02080.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1392+66_1392+72del others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 12/21 | chrX | 136685604 | ||||||
chrX:136686421 | T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-705A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686528 | ||||||
chrX:136686529 | TAC | T | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1246-708_1246-707d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686529 | ||||||
chrX:136686531 | C | T | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-711A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686534 | ||||||
chrX:136686535 | TTGCC | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-716_1246-713d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686535 | ||||||
chrX:136686541 | A | T | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-725C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686548 | ||||||
chrX:136686549 | TGGG | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-729_1246-727d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686549 | ||||||
chrX:136686552 | G | A | 2 | a0001c0001t0001g0242a0001c0001t0014g0116 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-735T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686558 | ||||||
chrX:136686561 | AC | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-739delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686561 | ||||||
chrX:136686564 | C | A | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0143a0001c0001t0001g0201a0001c0001t0002g0005 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0105a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0014g0116 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0109a0001c0001t0001g0233a0001c0001t0004g0042others(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 | a0001c0001t0001g0230a0001c0001t0001g0237a0001c0001t0017g0188 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0221others(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 | a0001c0001t0012g0240 | 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 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0094others(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 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0054others(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 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0148others(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 | GTATATAT others(1): Show |
1 | a0001c0001t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1246-779_1246-772d others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | ||||||
chrX:136686594 | G | GTGTA | 1 | a0001c0001t0001g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1246-772_1246-771i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686594 | ||||||
chrX:136686594 | G | GTGTATAT others(29): Show |
1 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0055others(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 | a0001c0001t0003g0239a0001c0001t0003g0246 | 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 | a0001c0001t0001g0046a0001c0001t0001g0214 | 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 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0061others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0003g0241 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0228 | 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 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(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:136686620 | AT | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-798delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686620 | ||||||
chrX:136686621 | T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0215a0001c0001t0002g0004 | 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 | T | TATATAC | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG01891.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1246-799_1246-798i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686621 | ||||||
chrX:136686621 | TACACATA others(15): Show |
T | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0063others(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 | CAT | 1 | a0001c0001t0001g0209 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1246-804_1246-803d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686625 | ||||||
chrX:136686625 | C | T | 14 | a0001c0001t0001g0105a0001c0001t0001g0214a0001c0001t0001g0232others(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 | a0001c0001t0001g0049a0001c0001t0001g0099a0001c0001t0001g0127others(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:136686625 | CATAT | C | 2 | a0001c0001t0005g0150a0001c0001t0005g0151 | 2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1246-806_1246-803d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686625 | ||||||
chrX:136686627 | T | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0062others(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 | a0001c0001t0002g0005 | 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 | a0001c0001t0003g0236 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0004g0229 | 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 | TAATATAT others(1): Show |
1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-807_1246-806i others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | ||||||
chrX:136686629 | T | TAC | 2 | a0001c0002t0002g0113a0001c0002t0002g0171 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1246-807_1246-806i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | ||||||
chrX:136686629 | T | TACAC | 1 | a0001c0002t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1246-807_1246-806i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | ||||||
chrX:136686629 | T | TATATACA others(1): Show |
1 | a0001c0002t0002g0130 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1246-807_1246-806i others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686629 | ||||||
chrX:136686629 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0004 | 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 | a0001c0001t0001g0133 | 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 | a0001c0002t0002g0113a0001c0002t0002g0171 | 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:136686639 | TATAC | T | 1 | a0001c0001t0001g0003 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1246-820_1246-817d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686639 | ||||||
chrX:136686641 | T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0228 | 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 | a0001c0001t0001g0001a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0094others(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 | CA | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1246-825dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686647 | ||||||
chrX:136686647 | C | T | 4 | a0001c0001t0001g0112a0001c0001t0004g0042a0001c0001t0004g0096others(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:136686647 | CAT | C | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1246-826_1246-825d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686647 | ||||||
chrX:136686666 | GTA | G | 1 | a0001c0001t0001g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1246-845_1246-844d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686666 | ||||||
chrX:136686681 | CAT | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0099others(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 | a0001c0001t0001g0243a0001c0001t0001g0244 | 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 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(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 | CAT | C | 1 | a0001c0001t0014g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1246-876_1246-875d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686697 | ||||||
chrX:136686697 | CATATATA others(21): Show |
C | 1 | a0001c0001t0001g0144 | 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:136686703 | T | TATAC | 1 | a0001c0001t0001g0029 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1246-881_1246-880i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686703 | ||||||
chrX:136686705 | T | TAC | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030 | 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:136686705 | TATAC | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0242 | 2 | HG02970.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1246-886_1246-883d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686705 | ||||||
chrX:136686707 | T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0245a0001c0002t0002g0113 | 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:136686707 | T | TATAC | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1246-885_1246-884i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686707 | ||||||
chrX:136686709 | C | CAT | 34 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0070others(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 | a0001c0001t0001g0068a0001c0001t0001g0173a0001c0001t0001g0178others(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 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0087others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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 | 2 | a0001c0001t0001g0033a0001c0001t0001g0242 | 2 | HG02970.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1246-888A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686711 | ||||||
chrX:136686717 | T | TATAC | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1246-895_1246-894i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136686717 | ||||||
chrX:136686717 | T | TATATACA others(13): Show |
1 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0118others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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:136687662 | AC | A | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1245+269delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 11/21 | chrX | 136687662 | ||||||
chrX:136688104 | G | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0087others(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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0007g0190 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0002g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1186-1238G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136689229 | ||||||
chrX:136689499 | CG | C | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1185+1110delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136689499 | ||||||
chrX:136690022 | TA | T | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1185+587delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136690022 | ||||||
chrX:136690279 | T | C | 1 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1185+61C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 10/21 | chrX | 136690549 | ||||||
chrX:136691059 | C | CA | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1047-312dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691059 | ||||||
chrX:136691200 | C | T | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-462T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691210 | ||||||
chrX:136691212 | G | GGCAC | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-465_1047-464i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691212 | ||||||
chrX:136691213 | A | C | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-472A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691220 | ||||||
chrX:136691222 | C | CAATA | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-475_1047-474i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691222 | ||||||
chrX:136691225 | A | T | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-508T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691256 | ||||||
chrX:136691265 | CTG | C | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-519_1047-518d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691265 | ||||||
chrX:136691269 | AT | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-522delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691269 | ||||||
chrX:136691280 | AG | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-533delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691280 | ||||||
chrX:136691287 | TTGTATG | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-545_1047-540d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691287 | ||||||
chrX:136691296 | TA | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-549delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691296 | ||||||
chrX:136691301 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-553T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691301 | ||||||
chrX:136691303 | AAAG | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-558_1047-556d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691303 | ||||||
chrX:136691310 | CTTA | C | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-565_1047-563d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691310 | ||||||
chrX:136691320 | TATCAA | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-577_1047-573d others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691320 | ||||||
chrX:136691327 | A | G | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-583T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691331 | ||||||
chrX:136691333 | TGAAG | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-589_1047-586d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691333 | ||||||
chrX:136691342 | TTA | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-596_1047-595d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691342 | ||||||
chrX:136691349 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-601T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691349 | ||||||
chrX:136691353 | CT | C | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-606delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691353 | ||||||
chrX:136691358 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-610T>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691358 | ||||||
chrX:136691368 | AAC | A | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-622_1047-621d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691368 | ||||||
chrX:136691371 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-623A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691371 | ||||||
chrX:136691376 | GAAAA | G | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-632_1047-629d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691376 | ||||||
chrX:136691385 | TA | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-638delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691385 | ||||||
chrX:136691389 | A | T | 1 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-648A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691396 | ||||||
chrX:136691403 | TGTG | T | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1047-658_1047-656d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691403 | ||||||
chrX:136691943 | C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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:136691999 | C | CA | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1047-1252dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136691999 | ||||||
chrX:136692032 | A | G | 1 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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 | a0001c0001t0009g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1047-1633G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136692381 | ||||||
chrX:136693114 | ATGAC | A | 1 | a0001c0001t0011g0174 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1047-2370_1047-236 others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693114 | ||||||
chrX:136693336 | C | A | 4 | a0001c0001t0001g0245a0001c0001t0004g0042a0001c0001t0004g0111others(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:136693344 | CA | C | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1047-2597delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693344 | ||||||
chrX:136693566 | G | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0121a0001c0001t0001g0144 | 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 | a0002c0004t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047-3049G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693797 | ||||||
chrX:136693865 | CG | C | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1047-3118delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693865 | ||||||
chrX:136693988 | CT | C | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1047-3241delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136693988 | ||||||
chrX:136694056 | C | CT | 33 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136694056 | C | CTTT | 3 | a0001c0001t0001g0114a0001c0001t0002g0207a0001c0001t0002g0208 | 3 | HG01243.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1047-3311_1047-330 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694056 | ||||||
chrX:136694056 | CT | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0181 | 2 | HG00323.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1047-3309delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694056 | ||||||
chrX:136694198 | G | A | 1 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0072a0001c0001t0001g0089 | 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:136694606 | AC | A | 1 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047-3859delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136694606 | ||||||
chrX:136694716 | G | A | 1 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0243a0001c0001t0001g0244 | 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 | a0001c0001t0020g0098 | 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 | a0001c0001t0015g0224 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0058 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1047-5349C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696097 | ||||||
chrX:136696136 | G | GT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1047-5389dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136696136 | ||||||
chrX:136696166 | A | G | 1 | a0001c0001t0001g0032 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0002t0001g0117a0001c0002t0002g0113a0001c0002t0002g0130others(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 | a0001c0001t0001g0051a0001c0001t0016g0034 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0112 | 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 | a0001c0002t0001g0117a0001c0002t0002g0113a0001c0002t0002g0130 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(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 | a0001c0001t0001g0102a0001c0001t0001g0103 | 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 | a0001c0001t0001g0062 | 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 | a0001c0002t0001g0117a0001c0002t0002g0113a0001c0002t0002g0130 | 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 | a0001c0002t0002g0171 | 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 | a0001c0001t0001g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1046+8050C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136698858 | ||||||
chrX:136699205 | AT | A | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+7702delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699205 | ||||||
chrX:136699437 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1046+7471G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699437 | ||||||
chrX:136699453 | A | AT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+7454dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699453 | ||||||
chrX:136699513 | A | AT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+7394dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699513 | ||||||
chrX:136699542 | T | C | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 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 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1046+7309C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699599 | ||||||
chrX:136699865 | G | GT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+7042_1046+704 others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699865 | ||||||
chrX:136699902 | CT | C | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+7005delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136699902 | ||||||
chrX:136699995 | T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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 | a0001c0001t0001g0173a0001c0001t0011g0174 | 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:136700138 | A | AC | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6769dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700138 | ||||||
chrX:136700179 | CA | C | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6728delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700179 | ||||||
chrX:136700181 | G | T | 1 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0062 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1046+6660C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700248 | ||||||
chrX:136700286 | A | AG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6621dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700286 | ||||||
chrX:136700333 | T | TG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6574dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700333 | ||||||
chrX:136700362 | T | TA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6545dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700362 | ||||||
chrX:136700387 | C | T | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136700389 | T | TG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6518dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700389 | ||||||
chrX:136700528 | G | GGAA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6377_1046+637 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700528 | ||||||
chrX:136700533 | G | GA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6374dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700533 | ||||||
chrX:136700550 | G | GC | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6357dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700550 | ||||||
chrX:136700596 | G | GC | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6311dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700596 | ||||||
chrX:136700636 | C | CA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6271dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700636 | ||||||
chrX:136700707 | T | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0228 | 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 | a0001c0001t0007g0120a0001c0001t0007g0190 | 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:136700837 | C | CA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+6070dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136700837 | ||||||
chrX:136700887 | A | G | 1 | a0001c0001t0001g0228 | 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 | a0003c0003t0001g0180 | 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 | a0001c0001t0001g0242a0001c0001t0014g0116 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136701279 | C | CA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5628dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701279 | ||||||
chrX:136701336 | G | A | 12 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0003g0241 | 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 | a0001c0001t0001g0055a0001c0001t0001g0056 | 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:136701438 | T | TA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5469dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701438 | ||||||
chrX:136701449 | C | CA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5458dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701449 | ||||||
chrX:136701544 | GA | G | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5363delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701544 | ||||||
chrX:136701580 | TA | T | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5327delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701580 | ||||||
chrX:136701621 | A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 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 | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0066others(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 | C | CTTT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+5203_1046+520 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | ||||||
chrX:136701702 | CT | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0114a0001c0001t0001g0115others(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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG00323.hp1 HG01081.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1046+5199_1046+520 others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701702 | ||||||
chrX:136701702 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0194others(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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0014g0116 | 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 | a0001c0001t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1046+4972A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701936 | ||||||
chrX:136701974 | T | TG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+4933dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136701974 | ||||||
chrX:136701989 | G | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0234a0001c0001t0001g0235 | 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:136702244 | T | TA | 1 | a0001c0001t0014g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1046+4663dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702244 | ||||||
chrX:136702258 | G | A | 12 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136702278 | GA | G | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+4629delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702278 | ||||||
chrX:136702416 | A | AT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+4491dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702416 | ||||||
chrX:136702451 | T | C | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136702754 | GA | G | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1046+4153delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702754 | ||||||
chrX:136702941 | A | C | 1 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136702961 | A | AC | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3946dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136702961 | ||||||
chrX:136702996 | A | G | 1 | a0001c0001t0020g0098 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0017g0188 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136703228 | G | GA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3679dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703228 | ||||||
chrX:136703275 | G | GA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3632dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703275 | ||||||
chrX:136703276 | A | G | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136703450 | A | AT | 2 | a0001c0001t0001g0020a0001c0001t0001g0216 | 2 | NA18967.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1046+3457dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703450 | ||||||
chrX:136703463 | T | TG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3444dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703463 | ||||||
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:136703528 | A | AT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3379dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703528 | ||||||
chrX:136703583 | C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0089 | 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:136703636 | C | CT | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3271dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703636 | ||||||
chrX:136703654 | C | T | 1 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136703710 | T | TG | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3197dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703710 | ||||||
chrX:136703765 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1046+3143C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703765 | ||||||
chrX:136703809 | A | AC | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3098dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703809 | ||||||
chrX:136703879 | C | CA | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+3028dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703879 | ||||||
chrX:136703902 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1046+3006C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136703902 | ||||||
chrX:136704062 | TG | T | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1046+2845delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136704062 | ||||||
chrX:136704083 | T | C | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0005g0131others(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 | a0001c0001t0002g0004 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136705044 | G | GT | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1046+1863dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705044 | ||||||
chrX:136705096 | G | A | 1 | a0005c0009t0006g0086 | 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 | a0001c0001t0001g0121a0001c0001t0001g0144 | 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:136705290 | C | CA | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1046+1617dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | 136705290 | ||||||
chrX:136705355 | C | T | 1 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0071a0001c0001t0001g0097a0001c0001t0006g0067 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0004g0229 | 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 | a0001c0001t0001g0014 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0012g0240others(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:136708188 | GA | G | 1 | a0003c0003t0001g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.923+486delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708188 | ||||||
chrX:136708201 | T | C | 1 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+318A>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708357 | ||||||
chrX:136708381 | T | TA | 4 | a0001c0001t0001g0012a0001c0001t0001g0173a0001c0001t0011g0174others(1): Show | 4 | HG02080.hp1 HG02451.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+293dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708381 | ||||||
chrX:136708381 | T | TAA | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+292_923+293dup others(2): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 8/21 | chrX | 136708381 | ||||||
chrX:136708381 | TA | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0056others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0012g0240others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136709639 | TG | T | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.828-870delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136709639 | ||||||
chrX:136709738 | G | T | 1 | a0001c0002t0002g0171 | 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 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0022others(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 | a0001c0001t0001g0043a0001c0001t0001g0155a0001c0001t0001g0156others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0062a0001c0001t0001g0118a0001c0001t0001g0119others(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 | a0001c0001t0001g0133a0001c0001t0001g0143a0001c0001t0001g0159others(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 | a0001c0001t0005g0131 | 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 | a0001c0001t0001g0167a0001c0001t0001g0168 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136710330 | CATAT | C | 2 | a0001c0001t0001g0242a0001c0001t0004g0042 | 2 | HG02970.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.828-1564_828-1561d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136710330 | ||||||
chrX:136710448 | G | A | 1 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0012a0001c0001t0017g0188 | 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 | a0001c0002t0002g0130 | 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 | a0001c0001t0002g0207 | 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 | a0001c0002t0002g0113 | 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0068a0001c0001t0001g0178 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+1021A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136712255 | ||||||
chrX:136712426 | AT | A | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.827+849delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136712426 | ||||||
chrX:136712478 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.827+798T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136712478 | ||||||
chrX:136713002 | C | CT | 1 | a0001c0001t0001g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.827+273dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136713002 | ||||||
chrX:136713002 | CT | C | 2 | a0001c0001t0001g0138a0001c0001t0002g0207 | 2 | HG02886.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.827+273delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 7/21 | chrX | 136713002 | ||||||
chrX:136713782 | A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0232 | 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 | a0003c0003t0001g0180 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0004g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.733-1207T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714577 | ||||||
chrX:136714834 | T | TG | 1 | a0001c0001t0001g0054 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.733-1465dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136714834 | ||||||
chrX:136714864 | A | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0225a0001c0001t0001g0230others(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 | a0001c0001t0001g0109a0001c0001t0001g0225a0001c0001t0001g0230others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136715389 | G | GA | 1 | a0001c0001t0001g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.733-2020dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136715389 | ||||||
chrX:136716015 | A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136716328 | TG | T | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.733-2959delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136716328 | ||||||
chrX:136716576 | A | T | 1 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0074 | 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 | a0006c0008t0001g0124 | 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 | a0001c0001t0001g0245a0001c0001t0004g0219 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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:136717929 | A | G | 1 | a0001c0001t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.733-4559T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136717929 | ||||||
chrX:136717950 | C | T | 1 | a0001c0001t0001g0159 | 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 | a0001c0001t0002g0208 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0136a0001c0001t0001g0148 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(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 | T | TAA | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-5636_733-5635d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719004 | ||||||
chrX:136719004 | T | TAAAA | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-5638_733-5635d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719004 | ||||||
chrX:136719004 | TA | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0052others(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:136719004 | TAA | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0132 | 2 | HG02896.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.733-5636_733-5635d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719004 | ||||||
chrX:136719077 | G | GT | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-5708dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719077 | ||||||
chrX:136719534 | GA | G | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-6165delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719534 | ||||||
chrX:136719626 | A | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0153others(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:136719647 | TA | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-6278delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719647 | ||||||
chrX:136719686 | GA | G | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-6317delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136719686 | ||||||
chrX:136720093 | C | T | 1 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0056others(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 | a0001c0001t0012g0240 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.733-7135C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720505 | ||||||
chrX:136720505 | GA | G | 1 | a0001c0001t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733-7136delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720505 | ||||||
chrX:136720507 | A | G | 1 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0074 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.733-7171G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720541 | ||||||
chrX:136720566 | TA | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.733-7197delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720566 | ||||||
chrX:136720652 | T | C | 1 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0221others(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 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.733-7482A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720852 | ||||||
chrX:136720863 | C | CAATT | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733-7494_733-7493i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136720863 | ||||||
chrX:136720944 | A | C | 96 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0135others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0231a0001c0001t0003g0236 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0135others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0004others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0056others(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 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0035others(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:136724078 | CT | C | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+8023delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724078 | ||||||
chrX:136724161 | C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0197others(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:136724272 | G | GTT | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.732+7828_732+7829d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136724272 | ||||||
chrX:136724455 | A | C | 1 | a0001c0001t0001g0206 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0012a0001c0001t0001g0074a0001c0001t0001g0100others(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:136725363 | G | GCC | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.732+6737_732+6738d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725363 | ||||||
chrX:136725363 | GC | G | 10 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0114others(7): Show | 10 | HG01496.hp2 HG02145.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+6738delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725363 | ||||||
chrX:136725371 | C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0049others(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:136725373 | CA | C | 2 | a0001c0001t0001g0218a0003c0003t0002g0212 | 2 | NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.732+6728delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725373 | ||||||
chrX:136725781 | G | A | 2 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136725847 | GA | G | 1 | a0001c0001t0002g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.732+6254delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136725847 | ||||||
chrX:136726060 | A | G | 5 | a0001c0001t0005g0131a0001c0001t0005g0147a0001c0001t0005g0150others(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 | a0001c0001t0006g0067 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0019g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.732+5414A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726688 | ||||||
chrX:136726969 | TCCA | T | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.732+5130_732+5132d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136726969 | ||||||
chrX:136727305 | G | GTCTT | 32 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(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 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0061others(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 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0083others(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 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0066others(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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0193others(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 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0063others(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 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0092others(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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0135a0001c0001t0001g0154a0001c0001t0001g0159others(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 | TTCTCTTT others(1): Show |
1 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | 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 | TTCTTC | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.732+4776_732+4777i others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727325 | ||||||
chrX:136727325 | T | TTCTTTTT others(1): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0100others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0060others(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 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0148others(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 | T | TTTTC | 1 | a0001c0001t0001g0010 | 1 | NA18963.hp1 | 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 | TTTTC | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0031others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(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 | a0002c0004t0001g0128 | 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 | a0001c0006t0001g0041 | 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:136727326 | T | TC | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.732+4775_732+4776i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727326 | ||||||
chrX:136727326 | T | TCTTTCTC | 1 | a0001c0002t0002g0113 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.732+4775_732+4776i others(9): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727326 | ||||||
chrX:136727326 | TTTC | T | 1 | a0001c0001t0001g0016 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.732+4773_732+4775d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727326 | ||||||
chrX:136727327 | T | C | 70 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0052others(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 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0001g0054others(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 | a0001c0001t0001g0143a0001c0001t0001g0176a0001c0001t0002g0208 | 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 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0092others(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:136727333 | CT | C | 1 | a0003c0003t0002g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.732+4768delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727333 | ||||||
chrX:136727335 | T | C | 1 | a0002c0004t0013g0172 | 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 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0063others(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 | a0002c0004t0001g0128 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0193others(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 | a0001c0001t0001g0027a0001c0001t0001g0055a0001c0001t0001g0066others(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 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0030others(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 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0061others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0083others(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 | a0001c0001t0001g0052a0001c0001t0001g0082 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0090a0001c0001t0020g0098 | 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 | a0001c0001t0009g0064 | 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(2): Show |
C | 1 | a0001c0001t0001g0085 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.732+4712_732+4720d others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727381 | ||||||
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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0080a0001c0001t0001g0109a0001c0001t0001g0160others(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:136727386 | TTTCTTTC | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.732+4709_732+4715d others(9): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727386 | ||||||
chrX:136727387 | T | TTC | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.732+4713_732+4714d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727387 | ||||||
chrX:136727387 | TTCTTTCT others(3): Show |
T | 3 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0155 | 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 | a0001c0001t0001g0161a0001c0001t0001g0195a0001c0001t0001g0211others(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:136727390 | TTTC | T | 1 | a0001c0001t0001g0187 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.732+4709_732+4711d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727390 | ||||||
chrX:136727391 | T | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0057others(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:136727391 | TTCTTTC | T | 1 | a0001c0001t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.732+4705_732+4710d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727391 | ||||||
chrX:136727393 | CT | C | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.732+4708delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727393 | ||||||
chrX:136727393 | CTT | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0136a0001c0001t0001g0141others(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:136727394 | T | TTTC | 2 | a0001c0001t0001g0156a0001c0001t0001g0192 | 2 | HG01081.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.732+4705_732+4707d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727394 | ||||||
chrX:136727395 | T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0016a0001c0001t0001g0170a0001c0001t0001g0200 | 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 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0068others(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 | TTCTCTC | 1 | a0001c0001t0001g0140 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.732+4701_732+4706d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | ||||||
chrX:136727395 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0199 | 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 | a0001c0001t0011g0174 | 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:136727395 | TTC | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0045 | 2 | HG01168.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.732+4705_732+4706d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727395 | ||||||
chrX:136727397 | C | CT | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+4704dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727397 | ||||||
chrX:136727397 | C | CTT | 13 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0143others(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 | a0001c0001t0001g0163a0001c0001t0001g0196a0001c0001t0001g0214others(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 | a0006c0008t0001g0124 | 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 | CTCT | 1 | a0001c0001t0001g0226 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.732+4688_732+4690d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | ||||||
chrX:136727411 | C | CTCTCTT | 2 | a0001c0001t0001g0006a0001c0001t0001g0112 | 2 | HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.732+4690_732+4691i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | ||||||
chrX:136727411 | C | CTCTT | 6 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0025others(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:136727411 | CTCTT | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0162 | 2 | NA19006.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.732+4687_732+4690d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727411 | ||||||
chrX:136727413 | CTT | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0242a0001c0001t0003g0204others(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:136727413 | CTTTCTT | C | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+4683_732+4688d others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727413 | ||||||
chrX:136727414 | T | TCTC | 1 | a0001c0001t0005g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.732+4687_732+4688i others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727414 | ||||||
chrX:136727415 | T | C | 101 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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:136727417 | CT | C | 2 | a0001c0001t0001g0144a0001c0001t0019g0134 | 2 | HG04115.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.732+4684delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727417 | ||||||
chrX:136727418 | T | TC | 3 | a0001c0001t0001g0123a0001c0001t0001g0179a0001c0001t0003g0142 | 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:136727418 | T | TCTC | 2 | a0001c0001t0001g0145a0001c0001t0007g0190 | 2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.732+4683_732+4684i others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727418 | ||||||
chrX:136727419 | T | C | 1 | a0001c0001t0005g0131 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.732+4683A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727419 | ||||||
chrX:136727421 | C | CTT | 2 | a0001c0002t0002g0171a0004c0005t0001g0093 | 2 | HG02615.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.732+4679_732+4680d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727421 | ||||||
chrX:136727458 | CTTCT | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0153others(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 | a0001c0001t0001g0127 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.732+4636A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727466 | ||||||
chrX:136727467 | T | TTC | 1 | a0001c0001t0001g0214 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.732+4633_732+4634d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727467 | ||||||
chrX:136727503 | TCCTC | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0210others(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:136727521 | C | G | 1 | a0001c0001t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.732+4581G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136727521 | ||||||
chrX:136727629 | G | C | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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 | a0001c0001t0001g0062a0001c0001t0001g0160a0001c0001t0001g0185others(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 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(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 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0047others(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 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0070others(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 | a0001c0001t0001g0035a0001c0001t0001g0040 | 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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0046others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0029others(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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0049others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0001c0001t0001g0066a0001c0001t0001g0112a0002c0004t0013g0172 | 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 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0133others(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 | a0001c0001t0001g0026a0001c0001t0001g0027 | 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 | a0001c0001t0002g0207 | 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:136729049 | TCTCTC | T | 2 | a0001c0001t0001g0038a0003c0003t0002g0212 | 2 | NA18941.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.732+3048_732+3052d others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729049 | ||||||
chrX:136729051 | TCTC | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0065a0001c0001t0001g0192others(1): Show | 4 | HG01255.hp1 HG02004.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+3048_732+3050d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729051 | ||||||
chrX:136729054 | C | CTCT | 1 | a0001c0001t0001g0084 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.732+3047_732+3048i others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729054 | ||||||
chrX:136729060 | C | T | 1 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0193 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.732+3033G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729069 | ||||||
chrX:136729071 | C | CCA | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.732+3030_732+3031i others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729071 | ||||||
chrX:136729072 | A | C | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.732+3030T>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729072 | ||||||
chrX:136729136 | GC | G | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+2965delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729136 | ||||||
chrX:136729144 | C | T | 1 | a0001c0001t0001g0063 | 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 | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): 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 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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:136729292 | AC | A | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+2809delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729292 | ||||||
chrX:136729467 | C | CA | 15 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0078others(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 | C | CAA | 3 | a0001c0001t0001g0016a0002c0004t0001g0128a0002c0004t0013g0172 | 3 | HG02451.hp1 HG02809.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.732+2633_732+2634d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729467 | ||||||
chrX:136729467 | CA | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136729467 | CAA | C | 2 | a0001c0001t0001g0110a0001c0001t0004g0042 | 2 | HG03041.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.732+2633_732+2634d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729467 | ||||||
chrX:136729479 | A | G | 1 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0152others(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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0069others(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 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0153others(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 | a0001c0001t0003g0239a0001c0001t0003g0246 | 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 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.732+2348G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729754 | ||||||
chrX:136729764 | AG | A | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+2337delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729764 | ||||||
chrX:136729829 | C | CA | 1 | a0001c0001t0001g0085 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.732+2272dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729829 | ||||||
chrX:136729850 | GA | G | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+2251delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729850 | ||||||
chrX:136729869 | AT | A | 1 | a0001c0001t0001g0020 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.732+2232delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136729869 | ||||||
chrX:136729992 | A | C | 1 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136730588 | C | CA | 2 | a0001c0001t0001g0085a0001c0001t0001g0187 | 2 | HG02135.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.732+1513dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136730588 | ||||||
chrX:136730806 | T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0112others(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 | a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(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:136732075 | AT | A | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.732+26delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | 136732075 | ||||||
chrX:136732464 | C | T | 1 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136733004 | CTCTTT | C | 1 | a0001c0001t0001g0054 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.662-837_662-833del others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733004 | ||||||
chrX:136733121 | CT | C | 2 | a0001c0001t0001g0181a0007c0007t0010g0021 | 2 | NA19056.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.662-950delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733121 | ||||||
chrX:136733129 | T | A | 1 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0088a0001c0001t0001g0118a0001c0002t0002g0113others(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:136733130 | T | TA | 1 | a0001c0001t0017g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.662-959dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733130 | ||||||
chrX:136733254 | C | T | 2 | a0001c0001t0014g0116a0001c0002t0001g0117 | 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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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:136733379 | AC | A | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.662-1208delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733379 | ||||||
chrX:136733392 | TA | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.662-1221delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136733392 | ||||||
chrX:136733546 | C | T | 1 | a0001c0001t0001g0084 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0083others(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 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.662-1933C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734105 | ||||||
chrX:136734227 | CT | C | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.662-2056delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734227 | ||||||
chrX:136734247 | C | T | 1 | a0001c0001t0001g0011 | 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 | a0002c0004t0013g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.662-2076C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734248 | ||||||
chrX:136734281 | TG | T | 1 | a0007c0007t0010g0021 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.662-2110delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136734281 | ||||||
chrX:136734655 | A | G | 3 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0035a0001c0001t0001g0038 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0024 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.662-4201A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736373 | ||||||
chrX:136736508 | G | C | 1 | a0001c0001t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.662-4336C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736508 | ||||||
chrX:136736618 | G | GATGTGT | 1 | a0001c0001t0001g0185 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.662-4447_662-4446i others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | G | GATGTGTG others(1): Show |
2 | a0001c0001t0001g0146a0001c0002t0002g0171 | 2 | HG02615.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.662-4447_662-4446i others(10): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | G | GATGTGTG others(3): Show |
94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0002g0207a0001c0001t0005g0151a0001c0001t0009g0064others(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 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0001g0094others(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 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0014g0116others(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 | a0002c0004t0013g0172 | 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 | a0001c0001t0001g0012a0001c0002t0002g0130 | 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:136736618 | G | GGT | 2 | a0001c0001t0001g0024a0001c0001t0003g0241 | 2 | HG00423.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.662-4448_662-4447d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | G | GGTGT | 1 | a0001c0001t0001g0022 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.662-4450_662-4447d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | G | GT | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.662-4447_662-4446i others(3): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | GGT | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0078 | 2 | HG00639.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.662-4448_662-4447d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736618 | GGTGT | G | 2 | a0001c0001t0001g0045a0001c0001t0004g0229 | 2 | HG01168.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.662-4450_662-4447d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136736618 | ||||||
chrX:136736619 | G | A | 2 | a0001c0001t0001g0146a0001c0002t0002g0171 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0176 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0016 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.662-5270C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737442 | ||||||
chrX:136737467 | C | CA | 3 | a0001c0001t0001g0039a0001c0001t0001g0198a0001c0001t0012g0240 | 3 | HG02132.hp1 HG03453.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.662-5296dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737467 | ||||||
chrX:136737467 | CA | C | 2 | a0001c0001t0002g0004a0001c0002t0002g0113 | 2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.662-5296delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136737467 | ||||||
chrX:136737545 | A | G | 1 | a0001c0001t0007g0120 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0075others(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 | a0001c0001t0001g0088a0001c0001t0002g0207a0002c0004t0001g0128others(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 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0069others(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 | a0001c0001t0001g0026a0001c0001t0002g0004a0001c0001t0002g0005others(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 | a0001c0001t0009g0064 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0003c0003t0001g0180 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0004others(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:136740003 | C | CATTATTA others(2): Show |
1 | a0001c0002t0002g0130 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661+3573_661+3581d others(11): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740003 | ||||||
chrX:136740072 | G | A | 107 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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:136740910 | G | A | 1 | a0001c0001t0001g0033 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.661+2675C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136740910 | ||||||
chrX:136740912 | T | G | 1 | a0001c0002t0002g0171 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(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:136741525 | CT | C | 1 | a0001c0001t0001g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.661+2059delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741525 | ||||||
chrX:136741535 | T | TG | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0112others(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:136741535 | T | TTGTG | 1 | a0001c0002t0002g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.661+2049_661+2050i others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741535 | ||||||
chrX:136741536 | TTTG | T | 3 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 3 | HG02451.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.661+2046_661+2048d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136741536 | ||||||
chrX:136741537 | T | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0004others(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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0004others(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 | a0003c0003t0001g0180 | 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 | a0001c0001t0003g0241 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0005g0131 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.661+996A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742589 | ||||||
chrX:136742661 | C | CA | 1 | a0001c0001t0001g0009 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.661+923dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742661 | ||||||
chrX:136742838 | GA | G | 3 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.661+685C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742900 | ||||||
chrX:136742991 | GA | G | 1 | a0001c0001t0001g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.661+593delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136742991 | ||||||
chrX:136743091 | AG | A | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.661+493delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743091 | ||||||
chrX:136743111 | CA | C | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.661+473delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743111 | ||||||
chrX:136743231 | C | A | 1 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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 | a0001c0001t0001g0082 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136743505 | TA | T | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.661+79delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 5/21 | chrX | 136743505 | ||||||
chrX:136744263 | T | C | 2 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136744306 | CT | C | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.460-521delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744306 | ||||||
chrX:136744363 | A | G | 3 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0208 | 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:136744738 | TG | T | 1 | a0001c0001t0001g0118 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.459+484delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 4/21 | chrX | 136744738 | ||||||
chrX:136744766 | T | C | 1 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0002c0004t0013g0172 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0009g0064 | 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 | a0001c0001t0006g0067 | 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0001c0001t0001g0104 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0049others(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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0049others(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 | a0001c0001t0001g0080a0001c0001t0001g0104a0001c0001t0001g0123others(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 | a0001c0001t0002g0004a0001c0001t0014g0116a0001c0002t0001g0117others(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 | a0001c0001t0001g0083a0001c0001t0001g0169a0001c0001t0002g0207others(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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0005g0131others(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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0205 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0005 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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 | a0001c0001t0001g0232a0001c0001t0001g0238 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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:136750180 | A | AG | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-2589dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750180 | ||||||
chrX:136750190 | A | C | 2 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136750202 | C | CT | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-2611dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750202 | ||||||
chrX:136750607 | T | C | 3 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136750729 | CT | C | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3138delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750729 | ||||||
chrX:136750804 | C | CT | 7 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0081others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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:136750830 | T | TC | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3239dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750830 | ||||||
chrX:136750842 | C | T | 1 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0075others(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:136750971 | TTTTG | T | 2 | a0001c0001t0001g0012a0001c0001t0002g0207 | 2 | HG02080.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.250-3383_250-3380d others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136750971 | ||||||
chrX:136751025 | T | TG | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3434dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751025 | ||||||
chrX:136751089 | A | G | 2 | a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0001g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.250-3536G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751128 | ||||||
chrX:136751160 | T | TC | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3569dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751160 | ||||||
chrX:136751245 | AT | A | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3654delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751245 | ||||||
chrX:136751256 | GC | G | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3665delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751256 | ||||||
chrX:136751272 | A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0083others(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:136751373 | GC | G | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3782delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751373 | ||||||
chrX:136751396 | CT | C | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-3805delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751396 | ||||||
chrX:136751483 | C | T | 1 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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:136751674 | TC | T | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.250-4083delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751674 | ||||||
chrX:136751827 | T | TG | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4236dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751827 | ||||||
chrX:136751843 | TG | T | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4252delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136751843 | ||||||
chrX:136752031 | A | G | 2 | a0001c0001t0007g0120a0001c0001t0007g0190 | 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 | a0001c0001t0002g0207a0002c0004t0001g0128a0002c0004t0013g0172 | 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:136752083 | G | GA | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4492dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752083 | ||||||
chrX:136752202 | T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0148 | 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 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.250-4665G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752257 | ||||||
chrX:136752315 | G | GC | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4724dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752315 | ||||||
chrX:136752336 | G | GA | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4745dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752336 | ||||||
chrX:136752337 | A | G | 1 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-4871A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752463 | ||||||
chrX:136752497 | CT | C | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4906delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752497 | ||||||
chrX:136752549 | C | T | 2 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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:136752590 | GA | G | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-4999delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752590 | ||||||
chrX:136752680 | G | GT | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-5089dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752680 | ||||||
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 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-5171G>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752763 | ||||||
chrX:136752776 | TA | T | 1 | a0001c0001t0001g0023 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.250-5185delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136752776 | ||||||
chrX:136752881 | T | C | 3 | a0001c0001t0012g0240a0002c0004t0001g0128a0002c0004t0013g0172 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0075others(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 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.250-5721A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753313 | ||||||
chrX:136753436 | C | CA | 1 | a0001c0001t0001g0170 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-5845dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136753436 | ||||||
chrX:136753587 | C | T | 1 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0002c0004t0001g0128 | 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 | a0001c0001t0001g0089 | 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 | a0002c0004t0013g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.250-6568C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754160 | ||||||
chrX:136754218 | AG | A | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.250-6627delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754218 | ||||||
chrX:136754256 | G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(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:136754332 | TC | T | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.250-6741delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754332 | ||||||
chrX:136754362 | G | A | 1 | a0001c0001t0005g0131 | 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 | a0001c0001t0001g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.250-6932C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754524 | ||||||
chrX:136754582 | C | CA | 3 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0115 | 3 | HG02145.hp1 HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.250-6991dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754582 | ||||||
chrX:136754582 | C | CAA | 4 | a0001c0001t0001g0007a0001c0001t0001g0110a0001c0001t0001g0112others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-6992_250-6991d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754582 | ||||||
chrX:136754582 | CA | C | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-6991delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754582 | ||||||
chrX:136754594 | AAAC | A | 3 | a0001c0001t0001g0228a0001c0001t0009g0064a0006c0008t0001g0124 | 3 | HG03041.hp2 HG03209.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.250-7005_250-7003d others(5): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754594 | ||||||
chrX:136754595 | AAC | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(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 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0050others(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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0112others(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 | a0001c0001t0001g0079a0001c0001t0001g0109a0001c0001t0002g0208 | 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:136754920 | A | AG | 1 | a0006c0008t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.250-7329dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136754920 | ||||||
chrX:136755060 | C | T | 1 | a0001c0001t0001g0049 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0002c0004t0001g0128 | 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 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0016g0034 | 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 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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:136755983 | A | AT | 2 | a0001c0001t0001g0112a0001c0002t0002g0171 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.250-8392dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136755983 | ||||||
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 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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 | a0001c0001t0009g0064 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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 | a0001c0001t0001g0112a0001c0002t0002g0171 | 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 | a0001c0001t0005g0150a0001c0001t0005g0151 | 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 | a0002c0004t0001g0128 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(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 | 59 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0033others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(56): 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(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 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0078others(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(1): Show |
1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250-10447_250-1044 others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | ||||||
chrX:136758031 | C | CTTTTTTT others(2): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0103others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-10448_250-1044 others(13): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | ||||||
chrX:136758031 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0026a0001c0001t0001g0102a0001c0001t0001g0106others(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 | a0001c0001t0001g0027a0001c0001t0001g0055 | 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 | CTTTT | C | 1 | a0001c0001t0003g0239 | 1 | HG01952.hp1 | 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 | CTTTTTTT others(1): Show |
C | 1 | a0001c0001t0001g0197 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.250-10447_250-1044 others(12): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758031 | ||||||
chrX:136758031 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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 | a0002c0004t0001g0128 | 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 | a0001c0001t0009g0064a0003c0003t0001g0180 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136758095 | G | GGCT | 1 | a0001c0001t0008g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.250-10506_250-1050 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758095 | ||||||
chrX:136758280 | T | C | 1 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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:136758622 | C | CT | 1 | a0001c0001t0004g0096 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.250-11031dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758622 | ||||||
chrX:136758622 | CT | C | 1 | a0001c0001t0001g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.250-11031delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758622 | ||||||
chrX:136758716 | A | AT | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-11125dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758716 | ||||||
chrX:136758766 | C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0220others(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 | a0001c0001t0001g0177 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.250-11290A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758882 | ||||||
chrX:136758942 | T | TA | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-11351dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758942 | ||||||
chrX:136758990 | AT | A | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-11399delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136758990 | ||||||
chrX:136759043 | A | AT | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-11452dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759043 | ||||||
chrX:136759236 | A | T | 1 | a0001c0001t0005g0175 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0245a0001c0001t0004g0219 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(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:136759627 | C | CAA | 1 | a0001c0001t0002g0005 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.250-12037_250-1203 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136759627 | ||||||
chrX:136759627 | CA | C | 3 | a0001c0001t0001g0205a0001c0001t0005g0131a0001c0001t0005g0175 | 3 | HG02027.hp1 NA18953.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.250-12036delT | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0220others(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 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.250-13331C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136760923 | ||||||
chrX:136761429 | T | TA | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-13838dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761429 | ||||||
chrX:136761721 | C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0004others(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 | a0001c0001t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-14252T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761844 | ||||||
chrX:136761910 | TTC | T | 1 | a0001c0001t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-14320_250-1431 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761910 | ||||||
chrX:136761912 | C | CT | 1 | a0001c0001t0001g0008 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.250-14321dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761912 | ||||||
chrX:136761912 | CT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0170others(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 | a0001c0001t0001g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250-14321A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761913 | ||||||
chrX:136761964 | T | TG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14373dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136761964 | ||||||
chrX:136762047 | TG | T | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14456delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762047 | ||||||
chrX:136762219 | TC | T | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14628delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762219 | ||||||
chrX:136762280 | T | TC | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14689dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762280 | ||||||
chrX:136762314 | A | AG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14723dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762314 | ||||||
chrX:136762326 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.250-14734A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762326 | ||||||
chrX:136762501 | TTC | T | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14911_250-1491 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762501 | ||||||
chrX:136762504 | T | C | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-14912A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762504 | ||||||
chrX:136762701 | A | AG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-15110dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762701 | ||||||
chrX:136762716 | TC | T | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-15125delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762716 | ||||||
chrX:136762772 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.250-15180C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762772 | ||||||
chrX:136762808 | T | TA | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-15217dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762808 | ||||||
chrX:136762926 | G | GA | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-15335dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136762926 | ||||||
chrX:136762969 | G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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:136763281 | GT | G | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.250-15690delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763281 | ||||||
chrX:136763346 | C | T | 1 | a0002c0004t0001g0128 | 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 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0001c0001t0001g0032 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.249+15544A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763870 | ||||||
chrX:136763907 | C | CA | 1 | a0001c0001t0001g0123 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.249+15506dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136763907 | ||||||
chrX:136764103 | C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0038others(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:136764168 | CA | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0201 | 2 | HG01496.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.249+15245delT | 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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0002t0002g0113 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0002t0002g0113 | 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 | a0001c0002t0002g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+14818G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764596 | ||||||
chrX:136764812 | TA | T | 1 | a0004c0005t0001g0093 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.249+14601delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764812 | ||||||
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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0112others(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:136764980 | TG | T | 1 | a0001c0001t0001g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.249+14433delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136764980 | ||||||
chrX:136765214 | T | C | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0200 | 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 | a0002c0004t0001g0128 | 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 | a0004c0005t0001g0093 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0003c0003t0002g0212 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0036 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.249+13033C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766381 | ||||||
chrX:136766384 | G | GT | 3 | a0001c0001t0001g0028a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG02074.hp1 HG02602.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.249+13029dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766384 | ||||||
chrX:136766392 | T | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | TGG | 4 | a0001c0001t0001g0197a0001c0001t0002g0005a0001c0001t0005g0175others(1): Show | 4 | HG02615.hp2 HG02630.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+13020_249+1302 others(6): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766392 | ||||||
chrX:136766392 | T | TGGG | 1 | a0001c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+13019_249+1302 others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766392 | ||||||
chrX:136766392 | T | TTG | 5 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0183others(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:136766439 | G | GC | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+12974dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766439 | ||||||
chrX:136766850 | TG | T | 1 | a0001c0001t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.249+12563delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136766850 | ||||||
chrX:136766957 | C | G | 9 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(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:136767067 | A | AG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+12346dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767067 | ||||||
chrX:136767239 | G | C | 1 | a0001c0001t0002g0207 | 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 | a0001c0001t0001g0177 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.249+12168G>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767246 | ||||||
chrX:136767307 | A | AC | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+12106dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767307 | ||||||
chrX:136767337 | C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0220others(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 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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:136767461 | C | CCCAG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+11949_249+1195 others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767461 | ||||||
chrX:136767475 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.249+11939A>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767475 | ||||||
chrX:136767553 | C | CG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+11860dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767553 | ||||||
chrX:136767623 | C | CG | 2 | a0001c0001t0001g0012a0001c0001t0005g0175 | 2 | HG02080.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.249+11790dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767623 | ||||||
chrX:136767710 | C | T | 1 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.249+11683C>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767731 | ||||||
chrX:136767838 | G | GAGC | 1 | a0001c0001t0001g0112 | 1 | NA19240.hp1 | 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 | GAGC | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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:136767883 | T | TG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+11530dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136767883 | ||||||
chrX:136767960 | G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 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 | a0001c0001t0001g0008a0001c0001t0001g0126a0001c0001t0001g0182 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0032 | 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 | a0002c0004t0013g0172 | 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 | a0001c0001t0009g0064 | 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 | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 243 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.249+10146C>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769268 | ||||||
chrX:136769346 | A | AG | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+10067dupC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769346 | ||||||
chrX:136769400 | G | GACTC | 1 | a0001c0001t0005g0175 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.249+10010_249+1001 others(8): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136769400 | ||||||
chrX:136769653 | G | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0203others(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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0065 | 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 | a0001c0006t0001g0041 | 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 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0203others(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:136770368 | A | AAAAAC | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.249+9041_249+9045d others(7): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136770368 | ||||||
chrX:136770631 | T | C | 1 | a0001c0001t0005g0175 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0003c0003t0002g0212 | 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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0220others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0081a0001c0001t0001g0094 | 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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(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 | a0001c0001t0003g0241 | 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 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0177 | 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 | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(104): 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:136774345 | G | GA | 3 | a0001c0001t0001g0079a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02683.hp1 HG02970.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.249+5068dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774345 | ||||||
chrX:136774650 | C | CA | 29 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0112others(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 | C | CAA | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | HG02922.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+4762_249+4763d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774650 | ||||||
chrX:136774650 | CA | C | 107 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.249+4763delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774650 | ||||||
chrX:136774650 | CAA | C | 1 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.249+4762_249+4763d others(4): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774650 | ||||||
chrX:136774742 | G | GA | 1 | a0001c0001t0001g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.249+4671dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774742 | ||||||
chrX:136774742 | GA | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0218 | 2 | HG03669.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.249+4671delT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136774742 | ||||||
chrX:136775196 | T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0002t0002g0113 | 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 | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(104): 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 | a0001c0001t0001g0039 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.249+4116G>A | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775298 | ||||||
chrX:136775599 | AG | A | 1 | a0003c0003t0001g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.249+3814delC | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775599 | ||||||
chrX:136775602 | G | C | 1 | a0003c0003t0001g0180 | 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 | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(42): Show | 45 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.249+3724A>G | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136775690 | ||||||
chrX:136776046 | C | CA | 1 | a0001c0001t0001g0245 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.249+3367dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776046 | ||||||
chrX:136776138 | G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(42): Show | 45 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.249+3276C>T | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136776138 | ||||||
chrX:136776259 | C | G | 102 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(99): 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 | a0004c0005t0001g0093 | 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 | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(104): 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 | a0001c0001t0001g0214a0001c0001t0001g0215 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(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 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0047others(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 | a0001c0001t0001g0031a0001c0001t0001g0053a0001c0001t0001g0054others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0112others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0094 | 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 | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(42): Show | 45 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(42): 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 | a0001c0001t0003g0204 | 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 | 46 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(43): Show | 46 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.249+1991dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136777422 | ||||||
chrX:136777597 | T | C | 57 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0002g0207 | 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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(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 |
36 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 36 | HG00639.hp2 HG00738.hp1 HG01071.hp2 others(33): 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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0051others(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 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0004g0096others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0012a0001c0001t0001g0100a0001c0001t0001g0101others(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 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(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 | a0001c0001t0001g0109a0001c0001t0001g0110 | 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 | 102 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(99): Show | 102 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(99): 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 | a0001c0001t0002g0208 | 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 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0210 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(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:136778490 | C | CT | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01433.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.249+923dupA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778490 | ||||||
chrX:136778490 | CT | C | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.249+923delA | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778490 | ||||||
chrX:136778504 | C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0220others(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:136778517 | CTT | C | 1 | a0003c0003t0002g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.249+895_249+896del others(2): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778517 | ||||||
chrX:136778608 | GC | G | 1 | a0001c0001t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.249+805delG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136778608 | ||||||
chrX:136778676 | G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 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:136779370 | C | CA | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01981.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.249+43dupT | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 2/21 | chrX | 136779370 | ||||||
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 | a0001c0001t0001g0009 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.166-189T>C | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136779686 | ||||||
chrX:136780382 | A | AC | 1 | a0001c0001t0001g0008 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.165+335dupG | ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 1/21 | chrX | 136780382 | ||||||
chrX:136780523 | G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0001c0001t0001g0001a0001c0001t0001g0220a0001c0001t0001g0221others(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 |