geneid | 393 |
---|---|
ensemblid | ENSG00000089820.17 |
hgncid | 674 |
symbol | ARHGAP4 |
name | Rho GTPase activating protein 4 |
refseq_nuc | NM_001666.5 |
refseq_prot | NP_001657.3 |
ensembl_nuc | ENST00000350060.10 |
ensembl_prot | ENSP00000203786.8 |
mane_status | MANE Select |
chr | chrX |
start | 153907378 |
end | 153926264 |
strand | - |
ver | v1.2 |
region | chrX:153907378-153926264 |
region5000 | chrX:153902378-153931264 |
regionname0 | ARHGAP4_chrX_153907378_153926264 |
regionname5000 | ARHGAP4_chrX_153902378_153931264 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 946 | 285 | 72 | 47 | 126 | 11 | 27 | 93 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0002 | 0/0 | 946 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0003 | 0/0 | 946 | 5 | 0 | 1 | 0 | 0 | 4 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0004 | 0/0 | 946 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0005 | 0/0 | 15 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0006 | 0/0 | 208 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0007 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0008 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0009 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0010 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0011 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0012 | 0/0 | 946 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0013 | 0/0 | 119 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0014 | 0/0 | 121 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2841 | 186 | 52 | 28 | 85 | 4 | 17 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0002 | 1/1 | 2841 | 74 | 4 | 17 | 36 | 6 | 9 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0003 | 0/0 | 2841 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0004 | 0/0 | 2841 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0005 | 0/0 | 2841 | 5 | 0 | 1 | 0 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0006 | 0/0 | 2841 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0007 | 0/0 | 2841 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0008 | 0/0 | 2841 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0009 | 0/0 | 2841 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0010 | 0/0 | 2841 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0011 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0012 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0013 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0014 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0015 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0016 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0017 | 0/0 | 2842 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0018 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0019 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0020 | 0/0 | 2842 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0021 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0022 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0023 | 0/0 | 2841 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
c0024 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 414 | 299 | 76 | 49 | 130 | 10 | 32 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
t0002 | 0/0 | 414 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
t0003 | 0/0 | 414 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
t0004 | 0/0 | 414 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
t0005 | 0/0 | 413 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 44 | 2 | 9 | 29 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0002 | 0/0 | 10 | 0 | 1 | 6 | 0 | 3 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0003 | 0/0 | 8 | 1 | 5 | 0 | 1 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0004 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0011 | 0/0 | 4 | 0 | 0 | 1 | 3 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0020 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2841 | 186 | 52 | 28 | 85 | 4 | 17 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0002 | 1/1 | 2841 | 74 | 4 | 17 | 36 | 6 | 9 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0003 | 0/0 | 2841 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0006 | 0/0 | 2841 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0007 | 0/0 | 2841 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0008 | 0/0 | 2841 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0009 | 0/0 | 2841 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0018 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0019 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0021 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0023 | 0/0 | 2841 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0002c0004 | 0/0 | 2841 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0003c0005 | 0/0 | 2841 | 5 | 0 | 1 | 0 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0004c0010 | 0/0 | 2841 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0005c0024 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0006c0020 | 0/0 | 2842 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0007c0013 | 0/0 | 2840 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0008c0014 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0009c0015 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0010c0017 | 0/0 | 2842 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0011c0016 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0012c0012 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0013c0011 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0014c0022 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3254 | 184 | 50 | 28 | 85 | 4 | 17 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0001t0003 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0002t0001 | 1/1 | 3254 | 73 | 4 | 17 | 35 | 6 | 9 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0002t0005 | 0/0 | 3253 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0003t0001 | 0/0 | 3254 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0006t0002 | 0/0 | 3254 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0007t0004 | 0/0 | 3254 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0008t0001 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0009t0001 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0018t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0019t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0021t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0001c0023t0001 | 0/0 | 3254 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0002c0004t0001 | 0/0 | 3254 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0003c0005t0001 | 0/0 | 3254 | 5 | 0 | 1 | 0 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0004c0010t0001 | 0/0 | 3254 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0005c0024t0001 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0006c0020t0001 | 0/0 | 3255 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0007c0013t0001 | 0/0 | 3253 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0008c0014t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0009c0015t0001 | 0/0 | 3256 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0010c0017t0001 | 0/0 | 3255 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0011c0016t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0012c0012t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0013c0011t0001 | 0/0 | 3253 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
a0014c0022t0001 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | copy fasta | chrX | 153902378 | 153931264 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 44 | 2 | 9 | 29 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 1 | 3 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0002 | 0/0 | 10 | 0 | 1 | 6 | 0 | 3 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0003 | 0/0 | 8 | 1 | 5 | 0 | 1 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0155 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0002t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0003t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0006t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0006t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0007t0004g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0008t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0008t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0009t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0018t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0019t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0021t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0001c0023t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0002c0004t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0002c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0002c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0002c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0002c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0003c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0003c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0003c0005t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0004c0010t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0004c0010t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0005c0024t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0006c0020t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0007c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0008c0014t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0009c0015t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0010c0017t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0011c0016t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0012c0012t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0013c0011t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
a0014c0022t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0152 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0153 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00673 | hp1 | a0001 | c0006 | t0002 | g0024 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00735 | hp2 | a0001 | c0007 | t0004 | g0034 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00741 | hp1 | a0003 | c0005 | t0001 | g0084 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01099 | hp1 | a0002 | c0004 | t0001 | g0157 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01516 | hp1 | a0001 | c0007 | t0004 | g0034 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0150 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01884 | hp1 | a0002 | c0004 | t0001 | g0037 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01891 | hp2 | a0011 | c0016 | t0001 | g0165 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01928 | hp1 | a0013 | c0011 | t0001 | g0063 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02004 | hp2 | a0001 | c0023 | t0001 | g0109 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02015 | hp1 | a0001 | c0018 | t0001 | g0135 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CDX | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02257 | hp1 | a0001 | c0021 | t0001 | g0062 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02738 | hp1 | a0003 | c0005 | t0001 | g0028 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02976 | hp2 | a0001 | c0008 | t0001 | g0103 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03130 | hp1 | a0002 | c0004 | t0001 | g0159 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03225 | hp1 | a0002 | c0004 | t0001 | g0037 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03239 | hp2 | a0003 | c0005 | t0001 | g0027 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03486 | hp1 | a0001 | c0008 | t0001 | g0067 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03540 | hp1 | a0002 | c0004 | t0001 | g0177 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03704 | hp1 | a0003 | c0005 | t0001 | g0027 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04184 | hp1 | a0003 | c0005 | t0001 | g0028 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04204 | hp1 | a0012 | c0012 | t0001 | g0141 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18612 | hp1 | a0001 | c0006 | t0002 | g0057 | EAS | CHB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18948 | hp1 | a0007 | c0013 | t0001 | g0064 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18993 | hp1 | a0006 | c0020 | t0001 | g0049 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18998 | hp2 | a0004 | c0010 | t0001 | g0121 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19006 | hp1 | a0009 | c0015 | t0001 | g0125 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19010 | hp1 | a0004 | c0010 | t0001 | g0134 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19030 | hp2 | a0001 | c0009 | t0001 | g0022 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19062 | hp1 | a0001 | c0002 | t0005 | g0139 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19063 | hp1 | a0008 | c0014 | t0001 | g0089 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19066 | hp1 | a0001 | c0006 | t0002 | g0024 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19076 | hp1 | a0014 | c0022 | t0001 | g0108 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19077 | hp1 | a0001 | c0006 | t0002 | g0058 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19078 | hp1 | a0005 | c0024 | t0001 | g0181 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19078 | hp2 | a0010 | c0017 | t0001 | g0124 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20129 | hp2 | a0001 | c0009 | t0001 | g0022 | AFR | ASW | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | TSI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0149 | EUR | TSI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20905 | hp1 | a0001 | c0019 | t0001 | g0138 | SAS | GIH | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA20300 | hp2 | a0002 | c0004 | t0001 | g0158 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0115 | REF | REF | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0155 | REF | REF | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
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:153907829
|
C | T | 1 | a0004 | 2 | NA18998.hp2 NA19010.hp1 |
missense_variant | MODERATE | c.2741G>A | p.Arg914His | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 2803/3254 | 2741/2841 | 914/946 | chrX | 153907829 | ||
chrX:153907856
|
C | CG | 1 | a0014 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.2713dupC | p.Arg905fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 2775/3254 | 2713/2841 | 905/946 | chrX | 153907856 | ||
chrX:153907869
|
TG | T | 1 | a0008 | 1 | NA19063.hp1 | frameshift_variant | HIGH | c.2700delC | p.Ser901fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 2762/3254 | 2700/2841 | 900/946 | chrX | 153907869 | ||
chrX:153909483
|
T | TC | 1 | a0005 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.2466dupG | p.Ser823fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/22 | 2528/3254 | 2466/2841 | 822/946 | chrX | 153909483 | ||
chrX:153909776
|
G | GC | 1 | a0005 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.2378dupG | p.Leu794fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2440/3254 | 2378/2841 | 793/946 | chrX | 153909776 | ||
chrX:153909841
|
C | A | 1 | a0003 | 5 | HG00741.hp1 HG02738.hp1 HG03239.hp2 others(2): Show |
missense_variant | MODERATE | c.2314G>T | p.Val772Leu | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2376/3254 | 2314/2841 | 772/946 | chrX | 153909841 | ||
chrX:153909843
|
T | TC | 2 | a0009a0010 | 2 | NA19006.hp1 NA19078.hp2 |
frameshift_variant | HIGH | c.2311dupG | p.Asp771fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2373/3254 | 2311/2841 | 771/946 | chrX | 153909843 | ||
chrX:153909852
|
C | T | 1 | a0006 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.2303G>A | p.Arg768Gln | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2365/3254 | 2303/2841 | 768/946 | chrX | 153909852 | ||
chrX:153909912
|
A | AC | 1 | a0009 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.2242dupG | p.Val748fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2304/3254 | 2242/2841 | 748/946 | chrX | 153909912 | ||
chrX:153910039
|
C | CT | 1 | a0014 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.2202_2203insA | p.Glu735fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/22 | 2264/3254 | 2202/2841 | 734/946 | chrX | 153910039 | ||
chrX:153910288
|
A | AC | 1 | a0008 | 1 | NA19063.hp1 | frameshift_variant | HIGH | c.2038dupG | p.Val680fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/22 | 2100/3254 | 2038/2841 | 680/946 | chrX | 153910288 | ||
chrX:153910596
|
G | A | 1 | a0011 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1832C>T | p.Ala611Val | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/22 | 1894/3254 | 1832/2841 | 611/946 | chrX | 153910596 | ||
chrX:153912721
|
TC | T | 1 | a0007 | 1 | NA18948.hp1 | frameshift_variant | HIGH | c.1520delG | p.Gly507fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/22 | 1582/3254 | 1520/2841 | 507/946 | chrX | 153912721 | ||
chrX:153913444
|
C | T | 1 | a0012 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1291G>A | p.Gly431Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 9/22 | 1353/3254 | 1291/2841 | 431/946 | chrX | 153913444 | ||
chrX:153920703
|
T | TG | 1 | a0006 | 1 | NA18993.hp1 | frameshift_variant | HIGH | c.603dupC | p.Thr202fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/22 | 665/3254 | 603/2841 | 201/946 | chrX | 153920703 | ||
chrX:153921489
|
G | A | 1 | a0002 | 6 | HG01099.hp1 HG01884.hp1 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.311C>T | p.Ala104Val | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/22 | 373/3254 | 311/2841 | 104/946 | chrX | 153921489 | ||
chrX:153921655
|
GA | G | 1 | a0013 | 1 | HG01928.hp1 | frameshift_variant | HIGH | c.221delT | p.Phe74fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2/22 | 283/3254 | 221/2841 | 74/946 | chrX | 153921655 | ||
chrX:153921674
|
T | TC | 1 | a0014 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.202dupG | p.Glu68fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2/22 | 264/3254 | 202/2841 | 68/946 | chrX | 153921674 | ||
chrX:153926166
|
G | GC | 1 | a0005 | 1 | NA19078.hp1 | frameshift_variant | HIGH | c.36dupG | p.Leu13fs | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/22 | 98/3254 | 36/2841 | 12/946 | chrX | 153926166 |
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:153909514
|
G | A | 1 | a0001c0008 | 2 | HG02976.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.2436C>T | p.Gly812Gly | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/22 | 2498/3254 | 2436/2841 | 812/946 | chrX | 153909514 | ||
chrX:153910034
|
G | A | 1 | a0001c0018 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2208C>T | p.Ala736Ala | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/22 | 2270/3254 | 2208/2841 | 736/946 | chrX | 153910034 | ||
chrX:153910296
|
C | T | 1 | a0001c0006 | 4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
synonymous_variant | LOW | c.2031G>A | p.Gln677Gln | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/22 | 2093/3254 | 2031/2841 | 677/946 | chrX | 153910296 | ||
chrX:153910347
|
G | A | 1 | a0001c0009 | 2 | NA19030.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1980C>T | p.Phe660Phe | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/22 | 2042/3254 | 1980/2841 | 660/946 | chrX | 153910347 | ||
chrX:153910547
|
C | T | 2 | a0001c0003a0001c0021 | 12 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
synonymous_variant | LOW | c.1881G>A | p.Pro627Pro | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/22 | 1943/3254 | 1881/2841 | 627/946 | chrX | 153910547 | ||
chrX:153910800
|
A | G | 17 | a0001c0001a0001c0003a0001c0006others(14): Show | 226 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(223): Show |
synonymous_variant | LOW | c.1716T>C | p.His572His | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/22 | 1778/3254 | 1716/2841 | 572/946 | chrX | 153910800 | ||
chrX:153910830
|
C | T | 1 | a0001c0007 | 2 | HG00735.hp2 HG01516.hp1 |
synonymous_variant | LOW | c.1686G>A | p.Glu562Glu | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/22 | 1748/3254 | 1686/2841 | 562/946 | chrX | 153910830 | ||
chrX:153913865
|
G | A | 1 | a0001c0019 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1047C>T | p.Cys349Cys | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 8/22 | 1109/3254 | 1047/2841 | 349/946 | chrX | 153913865 | ||
chrX:153921458
|
G | A | 1 | a0001c0021 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.342C>T | p.Ser114Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/22 | 404/3254 | 342/2841 | 114/946 | chrX | 153921458 | ||
chrX:153921790
|
G | A | 1 | a0001c0023 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.87C>T | p.Ser29Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2/22 | 149/3254 | 87/2841 | 29/946 | chrX | 153921790 |
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:153907407
|
G | A | 1 | a0001c0006t0002 | 4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 322 | chrX | 153907407 | |||||
chrX:153907505
|
T | A | 1 | a0001c0007t0004 | 2 | HG00735.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 224 | chrX | 153907505 | |||||
chrX:153907544
|
C | T | 1 | a0001c0001t0003 | 2 | HG02622.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*185G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 185 | chrX | 153907544 | |||||
chrX:153907700
|
CG | C | 1 | a0001c0002t0005 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 28 | chrX | 153907700 |
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:153908160
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0174a0001c0008t0001g0067others(1): Show | 4 | HG01884.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-198A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908160 | ||||||
chrX:153908184
|
GC | G | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2608-223delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908184 | ||||||
chrX:153908188
|
G | A | 1 | a0001c0002t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2608-226C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908188 | ||||||
chrX:153908199
|
C | A | 1 | a0001c0002t0001g0156 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2608-237G>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908199 | ||||||
chrX:153908298
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2608-336G>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908298 | ||||||
chrX:153908361
|
G | A | 3 | a0001c0006t0002g0024a0001c0006t0002g0057a0001c0006t0002g0058 | 4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-399C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908361 | ||||||
chrX:153908448
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2608-487dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908448 | ||||||
chrX:153908475
|
G | GC | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2608-514dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908475 | ||||||
chrX:153908476
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2608-514G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908476 | ||||||
chrX:153908497
|
CA | C | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2608-536delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908497 | ||||||
chrX:153908521
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 188 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2607+549A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908521 | ||||||
chrX:153908521
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2607+548delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908521 | ||||||
chrX:153908558
|
GC | G | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2607+511delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908558 | ||||||
chrX:153908563
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2607+507G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908563 | ||||||
chrX:153908590
|
G | GC | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2607+479dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908590 | ||||||
chrX:153908595
|
A | AC | 1 | a0001c0002t0005g0139 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2607+474dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908595 | ||||||
chrX:153908623
|
C | CT | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2607+446dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908623 | ||||||
chrX:153908935
|
T | TG | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2607+134dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908935 | ||||||
chrX:153908986
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2607+84G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908986 | ||||||
chrX:153909051
|
GC | G | 1 | a0001c0002t0001g0072 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2607+18delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153909051 | ||||||
chrX:153909203
|
TG | T | 1 | a0008c0014t0001g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2508-35delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909203 | ||||||
chrX:153909305
|
C | G | 3 | a0001c0001t0001g0066a0001c0008t0001g0067a0001c0008t0001g0103 | 3 | HG01884.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2508-136G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909305 | ||||||
chrX:153909365
|
T | TG | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.2507+77dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909365 | ||||||
chrX:153909398
|
A | G | 3 | a0001c0001t0001g0170a0001c0009t0001g0022a0002c0004t0001g0158 | 4 | HG02965.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2507+45T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909398 | ||||||
chrX:153909413
|
T | TG | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.2507+29dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909413 | ||||||
chrX:153909434
|
CT | C | 1 | a0005c0024t0001g0181 | 1 | NA19078.hp1 | splice_region_variant&intron_variant | LOW | c.2507+8delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909434 | ||||||
chrX:153909552
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2415-17G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/21 | chrX | 153909552 | ||||||
chrX:153909599
|
G | GC | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.2415-65dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/21 | chrX | 153909599 | ||||||
chrX:153909955
|
A | AG | 2 | a0001c0002t0001g0118a0012c0012t0001g0141 | 2 | HG01192.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2231-32dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/21 | chrX | 153909955 | ||||||
chrX:153909957
|
G | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0043a0001c0001t0001g0066others(5): Show | 12 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2231-33C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/21 | chrX | 153909957 | ||||||
chrX:153910132
|
G | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0013others(31): Show | 46 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.2156+39C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/21 | chrX | 153910132 | ||||||
chrX:153910169
|
A | AC | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | splice_donor_variant&intron_variant | HIGH | c.2156+1dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/21 | chrX | 153910169 | ||||||
chrX:153910416
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1923-12G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/21 | chrX | 153910416 | ||||||
chrX:153910439
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1923-35C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/21 | chrX | 153910439 | ||||||
chrX:153910623
|
G | GC | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1817-13dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/21 | chrX | 153910623 | ||||||
chrX:153910671
|
A | AC | 3 | a0001c0001t0001g0171a0010c0017t0001g0124a0014c0022t0001g0108 | 3 | HG02572.hp1 NA19076.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1816+28dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/21 | chrX | 153910671 | ||||||
chrX:153910889
|
G | GC | 1 | a0001c0002t0005g0139 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1681+32dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 14/21 | chrX | 153910889 | ||||||
chrX:153910915
|
TC | T | 1 | a0008c0014t0001g0089 | 1 | NA19063.hp1 | splice_region_variant&intron_variant | LOW | c.1681+6delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 14/21 | chrX | 153910915 | ||||||
chrX:153911010
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1604-11T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 13/21 | chrX | 153911010 | ||||||
chrX:153911107
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1603+22C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 13/21 | chrX | 153911107 | ||||||
chrX:153911191
|
TG | T | 1 | a0008c0014t0001g0089 | 1 | NA19063.hp1 | splice_region_variant&intron_variant | LOW | c.1543-3delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911191 | ||||||
chrX:153911202
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1543-13C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911202 | ||||||
chrX:153911252
|
C | CT | 29 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0020others(26): Show | 40 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.1543-64dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | ||||||
chrX:153911252
|
C | CTT | 2 | a0001c0001t0001g0113a0001c0001t0001g0167 | 2 | HG00597.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1543-65_1543-64dup others(2): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | ||||||
chrX:153911252
|
CT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 120 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1543-64delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | ||||||
chrX:153911252
|
CTT | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0001g0098others(3): Show | 7 | HG01928.hp1 HG02622.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543-65_1543-64del others(2): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | ||||||
chrX:153911505
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 190 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1543-316A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911505 | ||||||
chrX:153911858
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1543-669A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911858 | ||||||
chrX:153911916
|
T | TA | 2 | a0001c0002t0001g0072a0001c0002t0001g0129 | 2 | NA18968.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1543-728dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911916 | ||||||
chrX:153911916
|
TA | T | 5 | a0001c0002t0001g0117a0001c0002t0001g0132a0001c0002t0001g0133others(2): Show | 5 | HG01517.hp2 HG01943.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-728delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911916 | ||||||
chrX:153911930
|
A | AG | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 202 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1543-742_1543-741i others(3): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911930 | ||||||
chrX:153911930
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0055a0001c0001t0001g0163 | 3 | HG01168.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1543-741T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911930 | ||||||
chrX:153911934
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0170a0001c0009t0001g0022 | 4 | HG02109.hp2 HG02965.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-745C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911934 | ||||||
chrX:153912122
|
T | TC | 1 | a0001c0002t0005g0139 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1542+577dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912122 | ||||||
chrX:153912139
|
CTT | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0092 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1542+559_1542+560d others(4): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912139 | ||||||
chrX:153912141
|
T | C | 2 | a0001c0001t0001g0107a0011c0016t0001g0165 | 2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1542+559A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912141 | ||||||
chrX:153912210
|
C | CG | 1 | a0001c0001t0001g0096 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1542+489dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912210 | ||||||
chrX:153912211
|
G | A | 1 | a0001c0023t0001g0109 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1542+489C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912211 | ||||||
chrX:153912478
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1542+222T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912478 | ||||||
chrX:153912519
|
C | T | 1 | a0001c0002t0001g0077 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1542+181G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912519 | ||||||
chrX:153912528
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1542+172A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912528 | ||||||
chrX:153912610
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1542+90A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912610 | ||||||
chrX:153912969
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1439+55C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912969 | ||||||
chrX:153912986
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1439+38C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912986 | ||||||
chrX:153912992
|
TC | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0055others(2): Show | 5 | HG01099.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1439+31delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912992 | ||||||
chrX:153912994
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1439+30C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912994 | ||||||
chrX:153912999
|
G | A | 2 | a0001c0001t0001g0016a0001c0008t0001g0103 | 4 | HG02109.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1439+25C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912999 | ||||||
chrX:153913005
|
G | GC | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1439+18dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153913005 | ||||||
chrX:153913060
|
T | TG | 1 | a0001c0001t0001g0096 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1412-10dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 10/21 | chrX | 153913060 | ||||||
chrX:153913936
|
A | G | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1033-57T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153913936 | ||||||
chrX:153913961
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1033-82G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153913961 | ||||||
chrX:153914069
|
T | C | 1 | a0001c0002t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1033-190A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914069 | ||||||
chrX:153914076
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1033-197G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914076 | ||||||
chrX:153914266
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1033-387C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914266 | ||||||
chrX:153914388
|
T | TA | 1 | a0001c0002t0005g0139 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1033-510dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914388 | ||||||
chrX:153914482
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1033-603T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914482 | ||||||
chrX:153914590
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1033-711C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914590 | ||||||
chrX:153914794
|
G | A | 1 | a0001c0002t0001g0082 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1033-915C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914794 | ||||||
chrX:153914828
|
A | AT | 1 | a0010c0017t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1033-950dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914828 | ||||||
chrX:153914838
|
G | GT | 1 | a0010c0017t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1033-960_1033-959i others(3): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914838 | ||||||
chrX:153914892
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033-1013T>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914892 | ||||||
chrX:153914950
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1033-1071T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914950 | ||||||
chrX:153915008
|
G | GC | 1 | a0010c0017t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1033-1130dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915008 | ||||||
chrX:153915066
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0040others(17): Show | 26 | HG00673.hp1 HG01361.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1033-1187A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915066 | ||||||
chrX:153915119
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1033-1240C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915119 | ||||||
chrX:153915164
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033-1285T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915164 | ||||||
chrX:153915184
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0025others(10): Show | 24 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1033-1305C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915184 | ||||||
chrX:153915214
|
G | C | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1033-1335C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915214 | ||||||
chrX:153915214
|
G | T | 8 | a0001c0001t0001g0128a0001c0002t0001g0033a0001c0002t0001g0116others(5): Show | 9 | HG02027.hp1 NA18975.hp1 NA18989.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033-1335C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915214 | ||||||
chrX:153915223
|
A | AG | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1033-1345dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915223 | ||||||
chrX:153915228
|
T | TG | 1 | a0005c0024t0001g0181 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1033-1350dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915228 | ||||||
chrX:153915250
|
G | GA | 1 | a0010c0017t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1033-1372dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915250 | ||||||
chrX:153915301
|
T | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0015others(13): Show | 25 | HG00140.hp1 HG00597.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033-1422A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915301 | ||||||
chrX:153916741
|
C | CAAA | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+2088_1032+209 others(7): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916741 | ||||||
chrX:153916805
|
TG | T | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+2026delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916805 | ||||||
chrX:153916820
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1032+2012C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916820 | ||||||
chrX:153916824
|
TC | T | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+2007delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916824 | ||||||
chrX:153916835
|
TG | T | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1996delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916835 | ||||||
chrX:153917109
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 220 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.1032+1723T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917109 | ||||||
chrX:153917207
|
G | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 174 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1032+1625C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917207 | ||||||
chrX:153917246
|
TA | T | 1 | a0001c0002t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1032+1585delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917246 | ||||||
chrX:153917254
|
TA | T | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1577delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917254 | ||||||
chrX:153917502
|
TC | T | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1032+1329delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917502 | ||||||
chrX:153917522
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1032+1310C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917522 | ||||||
chrX:153917542
|
GC | G | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1289delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917542 | ||||||
chrX:153917550
|
GT | G | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1281delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917550 | ||||||
chrX:153917582
|
T | TC | 1 | a0001c0002t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1032+1249dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917582 | ||||||
chrX:153917637
|
TC | T | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1194delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917637 | ||||||
chrX:153917726
|
AG | A | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+1105delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917726 | ||||||
chrX:153917768
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1032+1064T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917768 | ||||||
chrX:153917863
|
T | C | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1032+969A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917863 | ||||||
chrX:153917873
|
G | GA | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+958dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917873 | ||||||
chrX:153917945
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032+887T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917945 | ||||||
chrX:153917976
|
A | AG | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+855dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917976 | ||||||
chrX:153918077
|
G | GA | 1 | a0005c0024t0001g0181 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1032+754dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918077 | ||||||
chrX:153918181
|
CA | C | 1 | a0014c0022t0001g0108 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1032+650delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918181 | ||||||
chrX:153918231
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1032+601A>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918231 | ||||||
chrX:153918251
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1032+581C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918251 | ||||||
chrX:153918279
|
GA | G | 1 | a0001c0002t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1032+552delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918279 | ||||||
chrX:153918319
|
TG | T | 1 | a0001c0002t0001g0072 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1032+512delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918319 | ||||||
chrX:153918576
|
T | C | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1032+256A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918576 | ||||||
chrX:153918583
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0001g0174others(3): Show | 7 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032+249T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918583 | ||||||
chrX:153918617
|
G | GT | 1 | a0009c0015t0001g0125 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1032+214dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918617 | ||||||
chrX:153918654
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1032+178G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918654 | ||||||
chrX:153918730
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1032+102C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918730 | ||||||
chrX:153918756
|
T | TG | 1 | a0001c0002t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1032+75dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918756 | ||||||
chrX:153919061
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.811-8C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 6/21 | chrX | 153919061 | ||||||
chrX:153919302
|
G | C | 1 | a0001c0003t0001g0038 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.682-19C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919302 | ||||||
chrX:153919362
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0036others(8): Show | 18 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-79C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919362 | ||||||
chrX:153919594
|
A | AC | 1 | a0010c0017t0001g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.682-312dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919594 | ||||||
chrX:153919791
|
T | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.682-508A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919791 | ||||||
chrX:153919792
|
A | AT | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.682-510dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919792 | ||||||
chrX:153919796
|
T | TTA | 4 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0061others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-514_682-513ins others(2): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919796 | ||||||
chrX:153919798
|
T | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0174a0001c0009t0001g0022 | 4 | HG02109.hp2 HG03453.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-515A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919798 | ||||||
chrX:153919947
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.682-664G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919947 | ||||||
chrX:153919948
|
G | A | 8 | a0001c0001t0001g0151a0001c0002t0001g0003a0001c0002t0001g0023others(5): Show | 16 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.682-665C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919948 | ||||||
chrX:153920192
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.681+434G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153920192 | ||||||
chrX:153920342
|
GC | G | 1 | a0001c0002t0001g0115 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.681+283delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153920342 | ||||||
chrX:153920362
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.681+264C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153920362 | ||||||
chrX:153920958
|
A | AG | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 307 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.498+138dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4/21 | chrX | 153920958 | ||||||
chrX:153921207
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.436-48C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921207 | ||||||
chrX:153921250
|
G | T | 2 | a0001c0001t0001g0065a0007c0013t0001g0064 | 2 | NA18947.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.436-91C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921250 | ||||||
chrX:153921296
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+69G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921296 | ||||||
chrX:153921580
|
GC | G | 1 | a0001c0009t0001g0022 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.272+24delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2/21 | chrX | 153921580 | ||||||
chrX:153921911
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-102C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153921911 | ||||||
chrX:153922019
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.68-210C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922019 | ||||||
chrX:153922059
|
GT | G | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-251delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922059 | ||||||
chrX:153922063
|
AG | A | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-255delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922063 | ||||||
chrX:153922147
|
TC | T | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-339delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922147 | ||||||
chrX:153922245
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0043others(11): Show | 19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-436G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922245 | ||||||
chrX:153922349
|
C | G | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 9 | HG01934.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-540G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922349 | ||||||
chrX:153922513
|
GC | G | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-705delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922513 | ||||||
chrX:153922752
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-943A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922752 | ||||||
chrX:153922762
|
C | G | 1 | a0001c0002t0001g0114 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.68-953G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922762 | ||||||
chrX:153922867
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.68-1058C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922867 | ||||||
chrX:153923062
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 9 | HG00597.hp2 HG01261.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-1253G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923062 | ||||||
chrX:153923087
|
C | CG | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1279dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923087 | ||||||
chrX:153923094
|
TG | T | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1286delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923094 | ||||||
chrX:153923157
|
C | CA | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.68-1349dupT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923157 | ||||||
chrX:153923234
|
C | T | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1425G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923234 | ||||||
chrX:153923238
|
A | AG | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1430dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923238 | ||||||
chrX:153923271
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0043others(11): Show | 19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-1462G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923271 | ||||||
chrX:153923305
|
C | T | 2 | a0001c0002t0001g0110a0001c0002t0001g0111 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.68-1496G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923305 | ||||||
chrX:153923402
|
T | TC | 1 | a0001c0001t0001g0166 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.68-1594dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923402 | ||||||
chrX:153923461
|
AC | A | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.68-1653delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923461 | ||||||
chrX:153923515
|
AC | A | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.68-1707delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923515 | ||||||
chrX:153923522
|
A | AG | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.68-1714dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923522 | ||||||
chrX:153923598
|
T | TG | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.68-1790dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923598 | ||||||
chrX:153923641
|
GC | G | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1833delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923641 | ||||||
chrX:153923716
|
GC | G | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1908delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923716 | ||||||
chrX:153923784
|
GT | G | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.68-1976delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923784 | ||||||
chrX:153923814
|
GT | G | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.68-2006delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923814 | ||||||
chrX:153923870
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0043others(11): Show | 19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-2061G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923870 | ||||||
chrX:153923886
|
T | TC | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.68-2078dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923886 | ||||||
chrX:153923926
|
CA | C | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.68-2118delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923926 | ||||||
chrX:153923977
|
C | T | 1 | a0001c0002t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+2159G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923977 | ||||||
chrX:153924021
|
C | T | 2 | a0001c0001t0001g0048a0001c0009t0001g0022 | 3 | HG02109.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.67+2115G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924021 | ||||||
chrX:153924097
|
TA | T | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.67+2038delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924097 | ||||||
chrX:153924181
|
TC | T | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67+1954delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924181 | ||||||
chrX:153924203
|
TG | T | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+1932delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924203 | ||||||
chrX:153924293
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67+1843C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924293 | ||||||
chrX:153924366
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 176 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.67+1770G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924366 | ||||||
chrX:153924381
|
CT | C | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.67+1754delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924381 | ||||||
chrX:153924400
|
G | A | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67+1736C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924400 | ||||||
chrX:153924420
|
T | G | 1 | a0011c0016t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67+1716A>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924420 | ||||||
chrX:153924444
|
TC | T | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+1691delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924444 | ||||||
chrX:153924461
|
TG | T | 1 | a0001c0002t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.67+1674delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924461 | ||||||
chrX:153924498
|
T | TC | 1 | a0001c0001t0001g0166 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.67+1637dupG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924498 | ||||||
chrX:153924554
|
AC | A | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.67+1581delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924554 | ||||||
chrX:153924570
|
AG | A | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+1565delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924570 | ||||||
chrX:153924640
|
TA | T | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+1495delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924640 | ||||||
chrX:153924919
|
A | G | 1 | a0001c0002t0001g0023 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.67+1217T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924919 | ||||||
chrX:153924919
|
AC | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.67+1216delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924919 | ||||||
chrX:153925009
|
AC | A | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.67+1126delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925009 | ||||||
chrX:153925083
|
C | CG | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.67+1052_67+1053ins others(1): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925083 | ||||||
chrX:153925088
|
TG | T | 2 | a0001c0001t0001g0051a0006c0020t0001g0049 | 2 | NA18993.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.67+1047delC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925088 | ||||||
chrX:153925252
|
A | AATGATGT others(33): Show |
1 | a0001c0001t0001g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.67+844_67+883dupGA others(38): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925252 | ||||||
chrX:153925281
|
CA | C | 1 | a0006c0020t0001g0049 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+854delT | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925281 | ||||||
chrX:153925547
|
AC | A | 1 | a0001c0001t0001g0169 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.67+588delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925547 | ||||||
chrX:153925713
|
C | G | 2 | a0001c0001t0001g0048a0001c0009t0001g0022 | 3 | HG02109.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.67+423G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925713 | ||||||
chrX:153925787
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0170a0001c0001t0001g0171others(3): Show | 10 | HG02280.hp1 HG02572.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+349A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925787 | ||||||
chrX:153925811
|
TC | T | 1 | a0001c0001t0001g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.67+324delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925811 | ||||||
chrX:153925814
|
G | A | 1 | a0001c0001t0001g0021 | 3 | HG02083.hp1 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.67+322C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925814 | ||||||
chrX:153925839
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0046 | 5 | HG01261.hp1 HG02293.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+297G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925839 | ||||||
chrX:153925893
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+243C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925893 | ||||||
chrX:153925894
|
AC | A | 1 | a0001c0002t0001g0175 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+241delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925894 | ||||||
chrX:153925898
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+238T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925898 | ||||||
chrX:153925903
|
G | A | 1 | a0001c0003t0001g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+233C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925903 | ||||||
chrX:153925992
|
G | A | 1 | a0002c0004t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+144C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925992 | ||||||
chrX:153926060
|
C | CG | 1 | a0001c0003t0001g0042 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67+75dupC | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153926060 | ||||||
chrX:153926119
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 9 | HG01934.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+17C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153926119 | ||||||
chrX:153926129
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG02451.hp1 HG02976.hp1 HG03041.hp1 |
splice_region_variant&intron_variant | LOW | c.67+7G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153926129 |