geneid | 7504 |
---|---|
ensemblid | ENSG00000047597.7 |
hgncid | 12811 |
symbol | XK |
name | X-linked Kx blood group antigen, Kell and VPS13A binding protein |
refseq_nuc | NM_021083.4 |
refseq_prot | NP_066569.1 |
ensembl_nuc | ENST00000378616.5 |
ensembl_prot | ENSP00000367879.3 |
mane_status | MANE Select |
chr | chrX |
start | 37685791 |
end | 37732130 |
strand | + |
ver | v1.2 |
region | chrX:37685791-37732130 |
region5000 | chrX:37680791-37737130 |
regionname0 | XK_chrX_37685791_37732130 |
regionname5000 | XK_chrX_37680791_37737130 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 444 | 219 | 68 | 37 | 80 | 5 | 27 | 65 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1335 | 210 | 59 | 37 | 80 | 5 | 27 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
c0002 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
c0003 | 0/0 | 1335 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3840 | 130 | 8 | 24 | 72 | 5 | 19 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0002 | 0/0 | 3840 | 30 | 10 | 8 | 5 | 0 | 7 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0003 | 0/0 | 3840 | 15 | 15 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0004 | 0/0 | 3840 | 10 | 7 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0005 | 0/0 | 3840 | 5 | 5 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0006 | 0/0 | 3840 | 4 | 4 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0007 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0008 | 0/0 | 3840 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0009 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0010 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0011 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0012 | 0/0 | 3840 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0013 | 0/0 | 3840 | 2 | 1 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0014 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0015 | 0/0 | 3840 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0016 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0017 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0018 | 0/0 | 3840 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0019 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0020 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0021 | 0/0 | 3840 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
t0022 | 0/0 | 3840 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 10 | 1 | 1 | 5 | 0 | 2 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0002 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0003 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1335 | 210 | 59 | 37 | 80 | 5 | 27 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0002 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0003 | 0/0 | 1335 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5174 | 130 | 8 | 24 | 72 | 5 | 19 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0002 | 0/0 | 5174 | 30 | 10 | 8 | 5 | 0 | 7 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0003 | 0/0 | 5174 | 15 | 15 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0004 | 0/0 | 5174 | 10 | 7 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0005 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0006 | 0/0 | 5174 | 4 | 4 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0008 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0009 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0011 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0012 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0013 | 0/0 | 5174 | 2 | 1 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0014 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0015 | 0/0 | 5174 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0016 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0017 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0018 | 0/0 | 5174 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0019 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0021 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0001t0022 | 0/0 | 5174 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0002t0005 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0002t0007 | 0/0 | 5174 | 3 | 3 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0002t0020 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
a0001c0003t0010 | 0/0 | 5174 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | copy fasta | chrX | 37680791 | 37737130 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 9 | 1 | 0 | 5 | 0 | 2 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0013g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0016g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0017g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0018g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0019g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0002t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
a0001c0003t0010g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01192 | hp1 | a0001 | c0001 | t0022 | g0001 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01255 | hp1 | a0001 | c0001 | t0013 | g0172 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02055 | hp1 | a0001 | c0002 | t0020 | g0034 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02132 | hp1 | a0001 | c0001 | t0016 | g0108 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0071 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02615 | hp2 | a0001 | c0002 | t0007 | g0149 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02622 | hp1 | a0001 | c0003 | t0010 | g0017 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02630 | hp1 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0143 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02809 | hp2 | a0001 | c0001 | t0021 | g0173 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02896 | hp1 | a0001 | c0002 | t0007 | g0147 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0066 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02897 | hp1 | a0001 | c0002 | t0007 | g0148 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03130 | hp1 | a0001 | c0001 | t0019 | g0022 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0019 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03490 | hp1 | a0001 | c0001 | t0015 | g0003 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0144 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ESN | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0174 | AFR | GWD | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18906 | hp2 | a0001 | c0003 | t0010 | g0017 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18944 | hp1 | a0001 | c0001 | t0018 | g0061 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | LWK | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19056 | hp1 | a0001 | c0001 | t0017 | g0095 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | YRI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ASW | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0128 | AFR | ASW | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | MSL | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | USA | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | USA | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0076 | REF | REF | XK_chrX_37680791_37737130 | XK | chrX | 37680791 | 37737130 |
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 |
---|
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:37686111
|
C | T | 1 | a0001c0002 | 7 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.150C>T | p.Leu50Leu | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/3 | 321/5174 | 150/1335 | 50/444 | chrX | 37686111 | ||
chrX:37727892
|
C | G | 1 | a0001c0003 | 2 | HG02622.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.765C>G | p.Leu255Leu | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 936/5174 | 765/1335 | 255/444 | chrX | 37727892 |
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:37685814
|
C | A | 1 | a0001c0001t0014 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/3 | 148 | chrX | 37685814 | |||||
chrX:37728551
|
A | T | 1 | a0001c0001t0002 | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*89A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 89 | chrX | 37728551 | |||||
chrX:37728952
|
G | A | 1 | a0001c0001t0015 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 490 | chrX | 37728952 | |||||
chrX:37729365
|
T | C | 1 | a0001c0002t0007 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 903 | chrX | 37729365 | |||||
chrX:37729392
|
A | G | 1 | a0001c0001t0022 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 930 | chrX | 37729392 | |||||
chrX:37729399
|
G | A | 4 | a0001c0001t0003a0001c0001t0006a0001c0001t0009others(1): Show | 23 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 937 | chrX | 37729399 | |||||
chrX:37729464
|
C | T | 1 | a0001c0003t0010 | 2 | HG02622.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1002C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1002 | chrX | 37729464 | |||||
chrX:37729566
|
T | A | 1 | a0001c0001t0011 | 2 | HG02630.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1104T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1104 | chrX | 37729566 | |||||
chrX:37729835
|
C | A | 1 | a0001c0001t0016 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1373C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1373 | chrX | 37729835 | |||||
chrX:37729845
|
G | A | 1 | a0001c0002t0007 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1383 | chrX | 37729845 | |||||
chrX:37729860
|
T | C | 1 | a0001c0001t0006 | 4 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1398T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1398 | chrX | 37729860 | |||||
chrX:37729930
|
G | A | 3 | a0001c0001t0004a0001c0001t0011a0001c0001t0014 | 13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1468G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1468 | chrX | 37729930 | |||||
chrX:37730297
|
A | G | 2 | a0001c0001t0013a0001c0001t0021 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1835A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1835 | chrX | 37730297 | |||||
chrX:37730347
|
C | T | 1 | a0001c0002t0020 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1885C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1885 | chrX | 37730347 | |||||
chrX:37730348
|
G | A | 1 | a0001c0001t0021 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1886G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1886 | chrX | 37730348 | |||||
chrX:37730426
|
C | T | 5 | a0001c0001t0005a0001c0001t0013a0001c0001t0019others(2): Show | 9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 1964 | chrX | 37730426 | |||||
chrX:37730605
|
G | T | 1 | a0001c0001t0018 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2143 | chrX | 37730605 | |||||
chrX:37730985
|
T | C | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(2): Show | 46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2523T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2523 | chrX | 37730985 | |||||
chrX:37731355
|
C | A | 2 | a0001c0001t0005a0001c0002t0005 | 5 | HG02809.hp1 HG03516.hp1 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2893C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 2893 | chrX | 37731355 | |||||
chrX:37731656
|
G | A | 2 | a0001c0001t0009a0001c0003t0010 | 4 | HG02622.hp1 HG03471.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3194G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3194 | chrX | 37731656 | |||||
chrX:37731812
|
A | T | 1 | a0001c0001t0002 | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3350A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3350 | chrX | 37731812 | |||||
chrX:37731829
|
A | G | 1 | a0001c0001t0017 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3367A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3367 | chrX | 37731829 | |||||
chrX:37732044
|
G | A | 1 | a0001c0001t0012 | 2 | HG02451.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3582G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 3/3 | 3582 | chrX | 37732044 |
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:37686554
|
G | T | 5 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(2): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.245+348G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37686554 | ||||||
chrX:37687108
|
G | T | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.245+902G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687108 | ||||||
chrX:37687115
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.245+909A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687115 | ||||||
chrX:37687158
|
A | ATC | 7 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(4): Show | 11 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+972_245+973dup others(2): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687158 | |||||
chrX:37687158
|
ATC | A | 3 | a0001c0001t0003g0170a0001c0001t0009g0169a0001c0003t0010g0017 | 4 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+972_245+973del others(2): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687158 | |||||
chrX:37687170
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0002g0007 | 3 | HG00639.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.245+974_245+983del others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687170 | |||||
chrX:37687194
|
T | TAC | 28 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 35 | HG00280.hp1 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.245+1019_245+1020d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687194
|
T | TACAC | 2 | a0001c0001t0014g0019a0001c0001t0019g0022 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.245+1017_245+1020d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687194
|
T | TACACAC | 1 | a0001c0001t0005g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.245+1015_245+1020d others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687194
|
TAC | T | 33 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0146others(30): Show | 38 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.245+1019_245+1020d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687194
|
TACAC | T | 1 | a0001c0001t0003g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245+1017_245+1020d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687194
|
TACACAC | T | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.245+1015_245+1020d others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687194 | |||||
chrX:37687226
|
C | CACAT | 3 | a0001c0001t0006g0023a0001c0001t0006g0024a0001c0001t0006g0025 | 3 | HG02818.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.245+1020_245+1021i others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687226 | ||||||
chrX:37687226
|
C | CAT | 1 | a0001c0001t0006g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.245+1020_245+1021i others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687226 | ||||||
chrX:37687233
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.245+1027A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687233 | ||||||
chrX:37687263
|
A | T | 1 | a0001c0001t0013g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.245+1057A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687263 | ||||||
chrX:37687272
|
A | AT | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.245+1079dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687272 | |||||
chrX:37687272
|
AT | A | 2 | a0001c0001t0001g0139a0001c0001t0002g0140 | 2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.245+1079delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37687272 | |||||
chrX:37687324
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.245+1118G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687324 | ||||||
chrX:37687339
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245+1133C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687339 | ||||||
chrX:37687366
|
C | T | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245+1160C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687366 | ||||||
chrX:37687488
|
A | G | 9 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0037others(6): Show | 9 | HG01891.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+1282A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687488 | ||||||
chrX:37687675
|
C | T | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245+1469C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687675 | ||||||
chrX:37687953
|
G | C | 3 | a0001c0001t0003g0170a0001c0001t0009g0169a0001c0003t0010g0017 | 4 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+1747G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37687953 | ||||||
chrX:37688027
|
A | ATTTC | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(18): Show | 28 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+1853_245+1856d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688027 | |||||
chrX:37688027
|
A | ATTTCTTT others(1): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.245+1849_245+1856d others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688027 | |||||
chrX:37688027
|
ATTTC | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0171a0001c0002t0020g0034 | 3 | HG02055.hp1 HG03834.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.245+1853_245+1856d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688027 | |||||
chrX:37688035
|
C | A | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.245+1829C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688035 | ||||||
chrX:37688048
|
TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0002g0131a0001c0001t0002g0150 | 2 | HG00639.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.245+1845_245+1855d others(13): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688048 | |||||
chrX:37688049
|
TTCTTTCT others(3): Show |
T | 24 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0132others(21): Show | 28 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.245+1845_245+1854d others(12): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688049 | |||||
chrX:37688051
|
CTTTCTTT others(4): Show |
C | 9 | a0001c0001t0003g0011a0001c0001t0003g0036a0001c0001t0003g0037others(6): Show | 10 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+1849_245+1859d others(13): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688051 | |||||
chrX:37688051
|
CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0003g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.245+1849_245+1860d others(14): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688051 | |||||
chrX:37688055
|
CTTTCT | C | 3 | a0001c0002t0007g0147a0001c0002t0007g0148a0001c0002t0007g0149 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.245+1853_245+1857d others(7): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688055 | |||||
chrX:37688055
|
CTTTCTT | C | 11 | a0001c0001t0003g0129a0001c0001t0003g0170a0001c0001t0006g0023others(8): Show | 12 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.245+1853_245+1858d others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688055 | |||||
chrX:37688057
|
TTC | T | 6 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(3): Show | 10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.245+1853_245+1854d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688057 | |||||
chrX:37688058
|
TC | T | 1 | a0001c0001t0004g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.245+1853delC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688058 | ||||||
chrX:37688059
|
C | CT | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02738.hp1 HG03688.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.245+1872dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
C | CTT | 2 | a0001c0001t0008g0125a0001c0001t0008g0126 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.245+1871_245+1872d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
C | CTTT | 1 | a0001c0001t0008g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245+1870_245+1872d others(5): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
C | CTTTCT | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.245+1856_245+1857i others(7): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
C | CTTTCTT | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.245+1856_245+1857i others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
CT | C | 1 | a0001c0001t0012g0066 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245+1872delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
CTT | C | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(3): Show | 6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.245+1871_245+1872d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
CTTTT | C | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.245+1869_245+1872d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688059
|
CTTTTT | C | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.245+1868_245+1872d others(7): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688059 | |||||
chrX:37688067
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.245+1861T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688067 | ||||||
chrX:37688188
|
G | C | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.245+1982G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688188 | ||||||
chrX:37688232
|
AT | A | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.245+2033delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37688232 | |||||
chrX:37688301
|
C | T | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+2095C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688301 | ||||||
chrX:37688318
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.245+2112G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688318 | ||||||
chrX:37688422
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.245+2216A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688422 | ||||||
chrX:37688759
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.245+2553G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688759 | ||||||
chrX:37688778
|
A | G | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.245+2572A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37688778 | ||||||
chrX:37689373
|
TA | T | 1 | a0001c0001t0001g0033 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.245+3172delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37689373 | |||||
chrX:37689535
|
G | A | 3 | a0001c0001t0002g0007a0001c0001t0002g0151a0001c0001t0002g0152 | 5 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+3329G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37689535 | ||||||
chrX:37689597
|
A | G | 65 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(62): Show | 75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.245+3391A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37689597 | ||||||
chrX:37690204
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+3998A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690204 | ||||||
chrX:37690222
|
T | A | 1 | a0001c0001t0002g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.245+4016T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690222 | ||||||
chrX:37690415
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.246-3871A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690415 | ||||||
chrX:37690739
|
G | C | 87 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(84): Show | 98 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.246-3547G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690739 | ||||||
chrX:37690934
|
T | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-3352T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690934 | ||||||
chrX:37690999
|
G | A | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(3): Show | 6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-3287G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37690999 | ||||||
chrX:37691214
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(9): Show | 20 | HG00621.hp1 HG01109.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.246-3072C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691214 | ||||||
chrX:37691294
|
T | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-2992T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691294 | ||||||
chrX:37691301
|
G | A | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.246-2985G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37691301 | ||||||
chrX:37691806
|
CA | C | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2478delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37691806 | |||||
chrX:37691904
|
T | TC | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2379dupC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37691904 | |||||
chrX:37692044
|
T | TG | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2241dupG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692044 | |||||
chrX:37692080
|
AT | A | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2203delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692080 | |||||
chrX:37692096
|
A | AT | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2185dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692096 | |||||
chrX:37692107
|
CT | C | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-2176delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692107 | |||||
chrX:37692427
|
G | GT | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1852dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692427 | |||||
chrX:37692519
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-1767G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692519 | ||||||
chrX:37692522
|
TC | T | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1761delC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692522 | |||||
chrX:37692591
|
TG | T | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1693delG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692591 | |||||
chrX:37692605
|
T | TG | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1679dupG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692605 | |||||
chrX:37692691
|
G | GT | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1595_246-1594i others(3): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692691 | ||||||
chrX:37692804
|
G | T | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.246-1482G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692804 | ||||||
chrX:37692889
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.246-1397G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692889 | ||||||
chrX:37692936
|
T | TG | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1347dupG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692936 | |||||
chrX:37692950
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.246-1336G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692950 | ||||||
chrX:37692962
|
A | AC | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0008g0125others(2): Show | 5 | HG02074.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.246-1315dupC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692962 | |||||
chrX:37692962
|
AC | A | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.246-1315delC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37692962 | |||||
chrX:37692971
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.246-1315C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37692971 | ||||||
chrX:37693061
|
C | CA | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.246-1224dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693061 | |||||
chrX:37693148
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.246-1138C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693148 | ||||||
chrX:37693306
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 8 | NA18944.hp1 NA18953.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.246-980A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693306 | ||||||
chrX:37693476
|
C | CGTGTGT | 1 | a0001c0002t0005g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.246-789_246-784dup others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(1): Show |
3 | a0001c0002t0005g0143a0001c0002t0005g0144a0001c0002t0020g0034 | 3 | HG02055.hp1 HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.246-791_246-784dup others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(3): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0154others(1): Show | 4 | HG02083.hp1 HG02818.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-793_246-784dup others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(5): Show |
32 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0079others(29): Show | 38 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.246-795_246-784dup others(12): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(7): Show |
26 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0028others(23): Show | 32 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.246-797_246-784dup others(14): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(9): Show |
88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 116 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.246-799_246-784dup others(16): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(11): Show |
12 | a0001c0001t0001g0032a0001c0001t0001g0059a0001c0001t0001g0103others(9): Show | 12 | HG02027.hp1 HG02970.hp1 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.246-801_246-784dup others(18): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(13): Show |
9 | a0001c0001t0001g0060a0001c0001t0001g0107a0001c0001t0001g0113others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.246-803_246-784dup others(20): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(15): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0109 | 2 | HG02135.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.246-805_246-784dup others(22): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693476
|
C | CGTGTGTG others(17): Show |
1 | a0001c0001t0005g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246-807_246-784dup others(24): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 37693476 | |||||
chrX:37693503
|
A | G | 4 | a0001c0002t0005g0142a0001c0002t0005g0143a0001c0002t0005g0144others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-783A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693503 | ||||||
chrX:37693667
|
T | C | 1 | a0001c0001t0004g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.246-619T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693667 | ||||||
chrX:37693738
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.246-548G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693738 | ||||||
chrX:37693962
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246-324G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693962 | ||||||
chrX:37693966
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246-320C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693966 | ||||||
chrX:37693996
|
G | T | 1 | a0001c0001t0003g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246-290G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37693996 | ||||||
chrX:37694061
|
A | C | 2 | a0001c0001t0006g0024a0001c0001t0006g0025 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.246-225A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37694061 | ||||||
chrX:37694230
|
G | A | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.246-56G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 1/2 | chrX | 37694230 | ||||||
chrX:37694765
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0059 | 3 | HG02683.hp1 NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.508+217T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37694765 | ||||||
chrX:37694998
|
A | G | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+450A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37694998 | ||||||
chrX:37695357
|
A | G | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+809A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695357 | ||||||
chrX:37695438
|
T | TA | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(3): Show | 6 | HG01255.hp1 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+902dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37695438 | |||||
chrX:37695438
|
TA | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0085a0001c0001t0001g0121others(6): Show | 10 | HG01358.hp1 HG01884.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+902delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37695438 | |||||
chrX:37695661
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0072others(2): Show | 6 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+1113C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695661 | ||||||
chrX:37695835
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.508+1287A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695835 | ||||||
chrX:37695857
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.508+1309C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37695857 | ||||||
chrX:37696326
|
C | G | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+1778C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696326 | ||||||
chrX:37696409
|
A | T | 4 | a0001c0002t0005g0142a0001c0002t0005g0143a0001c0002t0005g0144others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.508+1861A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696409 | ||||||
chrX:37696448
|
A | T | 5 | a0001c0001t0003g0129a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+1900A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696448 | ||||||
chrX:37696679
|
G | C | 65 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(62): Show | 75 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.508+2131G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37696679 | ||||||
chrX:37697184
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.508+2636A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37697184 | ||||||
chrX:37698511
|
G | A | 26 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(23): Show | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.508+3963G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698511 | ||||||
chrX:37698543
|
C | CA | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(37): Show | 51 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.508+4021dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | |||||
chrX:37698543
|
C | CAA | 5 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0003g0138others(2): Show | 5 | HG03139.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+4020_508+4021d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | |||||
chrX:37698543
|
CA | C | 40 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0067others(37): Show | 45 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.508+4021delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | |||||
chrX:37698543
|
CAA | C | 3 | a0001c0001t0002g0165a0001c0001t0003g0035a0001c0001t0003g0040 | 3 | HG02257.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.508+4020_508+4021d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | |||||
chrX:37698543
|
CAAA | C | 1 | a0001c0001t0003g0041 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.508+4019_508+4021d others(5): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37698543 | |||||
chrX:37698587
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0155 | 3 | HG02683.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.508+4039T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698587 | ||||||
chrX:37698592
|
G | A | 36 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(33): Show | 44 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.508+4044G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698592 | ||||||
chrX:37698760
|
C | T | 2 | a0001c0001t0003g0035a0001c0001t0003g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.508+4212C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698760 | ||||||
chrX:37698845
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.508+4297T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698845 | ||||||
chrX:37698964
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.508+4416C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37698964 | ||||||
chrX:37699180
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508+4632G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37699180 | ||||||
chrX:37699788
|
AT | A | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.508+5244delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37699788 | |||||
chrX:37700279
|
G | C | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+5731G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700279 | ||||||
chrX:37700301
|
G | A | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+5753G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700301 | ||||||
chrX:37700752
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.508+6204C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700752 | ||||||
chrX:37700770
|
C | T | 1 | a0001c0001t0013g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.508+6222C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37700770 | ||||||
chrX:37700930
|
C | CA | 1 | a0001c0001t0002g0156 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.508+6392dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37700930 | |||||
chrX:37701203
|
G | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+6655G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701203 | ||||||
chrX:37701348
|
CT | C | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.508+6804delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37701348 | |||||
chrX:37701452
|
G | C | 1 | a0001c0001t0009g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+6904G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701452 | ||||||
chrX:37701553
|
TCAC | T | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+7009_508+7011d others(5): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37701553 | |||||
chrX:37701619
|
TA | T | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.508+7075delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37701619 | |||||
chrX:37701675
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.508+7127G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701675 | ||||||
chrX:37701755
|
G | A | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+7207G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701755 | ||||||
chrX:37701835
|
TGGAGAGA others(1): Show |
T | 20 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(17): Show | 22 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.508+7288_508+7295d others(10): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701835 | ||||||
chrX:37701888
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+7340G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701888 | ||||||
chrX:37701984
|
C | T | 34 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(31): Show | 41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.508+7436C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37701984 | ||||||
chrX:37702313
|
G | C | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+7765G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702313 | ||||||
chrX:37702943
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.508+8395T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702943 | ||||||
chrX:37702967
|
A | G | 1 | a0001c0001t0005g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.508+8419A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37702967 | ||||||
chrX:37703258
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508+8710G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703258 | ||||||
chrX:37703339
|
C | T | 2 | a0001c0001t0006g0024a0001c0001t0006g0025 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.508+8791C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703339 | ||||||
chrX:37703374
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.508+8826G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703374 | ||||||
chrX:37703498
|
G | GA | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.508+8955dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37703498 | |||||
chrX:37703858
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.508+9310A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703858 | ||||||
chrX:37703863
|
A | G | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+9315A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37703863 | ||||||
chrX:37703902
|
C | CCAGA | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.508+9358_508+9361d others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37703902 | |||||
chrX:37704399
|
T | C | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.508+9851T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704399 | ||||||
chrX:37704503
|
C | G | 26 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(23): Show | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.508+9955C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704503 | ||||||
chrX:37704538
|
TA | T | 4 | a0001c0001t0001g0051a0001c0001t0013g0172a0001c0001t0013g0174others(1): Show | 4 | HG01255.hp1 HG02809.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+10000delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37704538 | |||||
chrX:37704558
|
G | A | 31 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(28): Show | 35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.508+10010G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704558 | ||||||
chrX:37704749
|
C | T | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+10201C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704749 | ||||||
chrX:37704783
|
C | T | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+10235C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704783 | ||||||
chrX:37704791
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0098 | 2 | HG03834.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.508+10243C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37704791 | ||||||
chrX:37705029
|
A | T | 2 | a0001c0001t0011g0135a0001c0001t0011g0136 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+10481A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705029 | ||||||
chrX:37705183
|
C | T | 72 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(69): Show | 82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+10635C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705183 | ||||||
chrX:37705212
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.508+10664A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705212 | ||||||
chrX:37705217
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.508+10669G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705217 | ||||||
chrX:37705241
|
C | G | 1 | a0001c0001t0003g0129 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508+10693C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705241 | ||||||
chrX:37705242
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0003g0129a0001c0001t0014g0019 | 3 | HG03195.hp1 HG03516.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.508+10694A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705242 | ||||||
chrX:37705289
|
C | CA | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508+10754dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705289 | |||||
chrX:37705289
|
CA | C | 31 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(28): Show | 35 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.508+10754delA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705289 | |||||
chrX:37705377
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.508+10829G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705377 | ||||||
chrX:37705383
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.508+10835T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705383 | ||||||
chrX:37705408
|
C | T | 5 | a0001c0001t0003g0129a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+10860C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705408 | ||||||
chrX:37705416
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.508+10868G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705416 | ||||||
chrX:37705426
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.508+10878T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705426 | ||||||
chrX:37705430
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0103 | 3 | NA18945.hp1 NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.508+10882T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705430 | ||||||
chrX:37705433
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0103 | 3 | NA18945.hp1 NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.508+10885A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705433 | ||||||
chrX:37705439
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.508+10891G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705439 | ||||||
chrX:37705451
|
C | CA | 29 | a0001c0001t0001g0014a0001c0001t0001g0093a0001c0001t0001g0103others(26): Show | 34 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.508+10917dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705451 | |||||
chrX:37705631
|
A | G | 1 | a0001c0001t0012g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+11083A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705631 | ||||||
chrX:37705830
|
G | A | 6 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(3): Show | 10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+11282G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37705830 | ||||||
chrX:37705919
|
A | AT | 52 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0002g0007others(49): Show | 58 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.508+11386dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705919 | |||||
chrX:37705919
|
A | ATT | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.508+11385_508+1138 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37705919 | |||||
chrX:37706217
|
T | A | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.508+11669T>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706217 | ||||||
chrX:37706332
|
A | T | 1 | a0001c0001t0018g0061 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.508+11784A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706332 | ||||||
chrX:37706573
|
G | A | 12 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(9): Show | 16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+12025G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706573 | ||||||
chrX:37706603
|
C | CT | 62 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(59): Show | 72 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.508+12064dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706603 | |||||
chrX:37706603
|
C | CTT | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022others(3): Show | 6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12063_508+1206 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706603 | |||||
chrX:37706631
|
A | T | 4 | a0001c0001t0001g0084a0001c0001t0004g0018a0001c0001t0004g0175others(1): Show | 5 | HG02451.hp2 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+12083A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37706631 | ||||||
chrX:37706980
|
CAGA | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0053others(5): Show | 12 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.508+12437_508+1243 others(7): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37706980 | |||||
chrX:37707243
|
G | A | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022others(3): Show | 6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12695G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707243 | ||||||
chrX:37707255
|
G | A | 6 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022others(3): Show | 6 | HG02809.hp1 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+12707G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707255 | ||||||
chrX:37707289
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.508+12741C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707289 | ||||||
chrX:37707302
|
G | A | 3 | a0001c0002t0007g0147a0001c0002t0007g0148a0001c0002t0007g0149 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.508+12754G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707302 | ||||||
chrX:37707342
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0002g0153 | 2 | HG03704.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.508+12794C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707342 | ||||||
chrX:37707343
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.508+12795G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707343 | ||||||
chrX:37707414
|
TGGCTGCC others(33): Show |
T | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508+12919_508+1295 others(44): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37707414 | |||||
chrX:37707449
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.508+12901C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707449 | ||||||
chrX:37707489
|
C | T | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.508+12941C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707489 | ||||||
chrX:37707509
|
AGGGCTCC others(33): Show |
A | 4 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0072others(1): Show | 5 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+12990_508+1302 others(44): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37707509 | |||||
chrX:37707529
|
C | T | 1 | a0001c0001t0004g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.508+12981C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707529 | ||||||
chrX:37707534
|
C | T | 6 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(3): Show | 10 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.508+12986C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707534 | ||||||
chrX:37707535
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0163 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.508+12987G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707535 | ||||||
chrX:37707589
|
G | A | 9 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(6): Show | 9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+13041G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707589 | ||||||
chrX:37707612
|
A | G | 72 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(69): Show | 82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+13064A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707612 | ||||||
chrX:37707614
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.508+13066C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707614 | ||||||
chrX:37707625
|
C | T | 7 | a0001c0001t0001g0052a0001c0001t0001g0088a0001c0001t0001g0091others(4): Show | 7 | HG01255.hp1 HG02809.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.508+13077C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707625 | ||||||
chrX:37707744
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.508+13196T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707744 | ||||||
chrX:37707803
|
T | C | 9 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(6): Show | 13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.508+13255T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707803 | ||||||
chrX:37707888
|
C | T | 12 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(9): Show | 16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+13340C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707888 | ||||||
chrX:37707891
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0085 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.508+13343G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707891 | ||||||
chrX:37707897
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+13349G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707897 | ||||||
chrX:37707915
|
C | A | 24 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(21): Show | 28 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.508+13367C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37707915 | ||||||
chrX:37708033
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0167 | 2 | NA18974.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.508+13485A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37708033 | ||||||
chrX:37708344
|
AG | A | 1 | a0001c0002t0007g0147 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.508+13799delG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37708344 | |||||
chrX:37708586
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.508+14038A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37708586 | ||||||
chrX:37708692
|
A | AC | 1 | a0001c0002t0007g0147 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.508+14147dupC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37708692 | |||||
chrX:37709021
|
G | A | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+14473G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709021 | ||||||
chrX:37709154
|
T | C | 12 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(9): Show | 16 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+14606T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709154 | ||||||
chrX:37709238
|
A | G | 68 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(65): Show | 78 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.508+14690A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709238 | ||||||
chrX:37709435
|
G | T | 68 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(65): Show | 78 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.508+14887G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709435 | ||||||
chrX:37709657
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.508+15109C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709657 | ||||||
chrX:37709661
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508+15113C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37709661 | ||||||
chrX:37710080
|
C | T | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+15532C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710080 | ||||||
chrX:37710177
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.508+15629G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710177 | ||||||
chrX:37710593
|
C | T | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508+16045C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710593 | ||||||
chrX:37710897
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.508+16349G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37710897 | ||||||
chrX:37711001
|
A | G | 2 | a0001c0001t0006g0023a0001c0001t0006g0043 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.508+16453A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711001 | ||||||
chrX:37711326
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509-16310G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711326 | ||||||
chrX:37711579
|
T | C | 9 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(6): Show | 9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-16057T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711579 | ||||||
chrX:37711853
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.509-15783G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37711853 | ||||||
chrX:37712233
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.509-15403C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712233 | ||||||
chrX:37712257
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120 | 3 | HG00621.hp1 NA18952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.509-15379C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712257 | ||||||
chrX:37712290
|
C | G | 47 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(44): Show | 53 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.509-15346C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712290 | ||||||
chrX:37712318
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509-15318C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37712318 | ||||||
chrX:37713408
|
A | G | 1 | a0001c0002t0005g0144 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-14228A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713408 | ||||||
chrX:37713445
|
A | G | 16 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(13): Show | 18 | HG01891.hp1 HG02145.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.509-14191A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713445 | ||||||
chrX:37713458
|
T | C | 3 | a0001c0001t0009g0128a0001c0001t0009g0169a0001c0003t0010g0017 | 4 | HG02622.hp1 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-14178T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713458 | ||||||
chrX:37713532
|
C | T | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-14104C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713532 | ||||||
chrX:37713602
|
C | CT | 9 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0020others(6): Show | 13 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.509-14021dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37713602 | |||||
chrX:37713602
|
CT | C | 1 | a0001c0001t0001g0079 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.509-14021delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37713602 | |||||
chrX:37713699
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0075a0001c0001t0001g0088others(3): Show | 6 | NA18986.hp1 NA19005.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-13937C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713699 | ||||||
chrX:37713700
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-13936G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37713700 | ||||||
chrX:37714319
|
T | C | 9 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(6): Show | 9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-13317T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714319 | ||||||
chrX:37714400
|
G | GA | 2 | a0001c0001t0006g0024a0001c0001t0006g0025 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.509-13227dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37714400 | |||||
chrX:37714454
|
A | C | 1 | a0001c0002t0020g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-13182A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714454 | ||||||
chrX:37714461
|
A | G | 1 | a0001c0002t0005g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509-13175A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714461 | ||||||
chrX:37714590
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.509-13046T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714590 | ||||||
chrX:37714922
|
A | G | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509-12714A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714922 | ||||||
chrX:37714941
|
A | T | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-12695A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37714941 | ||||||
chrX:37715015
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.509-12621A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715015 | ||||||
chrX:37715017
|
A | AGT | 1 | a0001c0001t0014g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509-12612_509-1261 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37715017 | |||||
chrX:37715024
|
G | GTA | 5 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(2): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-12598_509-1259 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37715024 | |||||
chrX:37715104
|
GTATA | G | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.509-12522_509-1251 others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37715104 | |||||
chrX:37715136
|
A | ATG | 1 | a0001c0001t0001g0078 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.509-12484_509-1248 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37715136 | |||||
chrX:37715279
|
T | C | 5 | a0001c0001t0004g0006a0001c0001t0004g0018a0001c0001t0004g0175others(2): Show | 9 | HG00735.hp1 HG01070.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-12357T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715279 | ||||||
chrX:37715671
|
C | A | 6 | a0001c0001t0003g0137a0001c0001t0003g0138a0001c0001t0003g0170others(3): Show | 7 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-11965C>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715671 | ||||||
chrX:37715823
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-11813T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715823 | ||||||
chrX:37715851
|
A | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-11785A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37715851 | ||||||
chrX:37716015
|
C | T | 1 | a0001c0001t0002g0007 | 3 | HG00639.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.509-11621C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716015 | ||||||
chrX:37716294
|
T | G | 3 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0019g0022 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509-11342T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716294 | ||||||
chrX:37716724
|
T | C | 1 | a0001c0001t0003g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-10912T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37716724 | ||||||
chrX:37716798
|
TTTTG | T | 1 | a0001c0001t0017g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.509-10822_509-1081 others(8): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37716798 | |||||
chrX:37717003
|
G | C | 3 | a0001c0002t0007g0147a0001c0002t0007g0148a0001c0002t0007g0149 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.509-10633G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717003 | ||||||
chrX:37717070
|
G | A | 4 | a0001c0001t0003g0170a0001c0001t0009g0128a0001c0001t0009g0169others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-10566G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717070 | ||||||
chrX:37717123
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.509-10513C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717123 | ||||||
chrX:37717230
|
C | CT | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-10405dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37717230 | |||||
chrX:37717359
|
T | TTC | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-10276_509-1027 others(6): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37717359 | |||||
chrX:37717652
|
T | TGA | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-9982_509-9981d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37717652 | |||||
chrX:37717743
|
A | G | 9 | a0001c0001t0005g0021a0001c0001t0005g0026a0001c0001t0013g0172others(6): Show | 9 | HG01255.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-9893A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717743 | ||||||
chrX:37717838
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.509-9798G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37717838 | ||||||
chrX:37718535
|
T | TA | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-9098dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37718535 | |||||
chrX:37718554
|
C | CT | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-9078dupT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37718554 | |||||
chrX:37718850
|
G | C | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-8786G>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37718850 | ||||||
chrX:37718914
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.509-8722A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37718914 | ||||||
chrX:37719158
|
A | G | 26 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(23): Show | 30 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.509-8478A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719158 | ||||||
chrX:37719249
|
G | T | 3 | a0001c0001t0003g0036a0001c0001t0003g0039a0001c0001t0003g0040 | 3 | HG02922.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.509-8387G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719249 | ||||||
chrX:37719696
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0049a0001c0001t0001g0072others(1): Show | 5 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-7940A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719696 | ||||||
chrX:37719797
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-7839T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719797 | ||||||
chrX:37719866
|
G | GA | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509-7763dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37719866 | |||||
chrX:37719973
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509-7663C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37719973 | ||||||
chrX:37720020
|
C | G | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-7616C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720020 | ||||||
chrX:37720169
|
A | G | 1 | a0001c0001t0009g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509-7467A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720169 | ||||||
chrX:37720351
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.509-7285A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720351 | ||||||
chrX:37720462
|
C | G | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-7174C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720462 | ||||||
chrX:37720760
|
A | C | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-6876A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720760 | ||||||
chrX:37720965
|
C | T | 1 | a0001c0002t0007g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509-6671C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37720965 | ||||||
chrX:37721260
|
T | C | 1 | a0001c0001t0002g0159 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.509-6376T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721260 | ||||||
chrX:37721534
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.509-6102A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721534 | ||||||
chrX:37721579
|
G | T | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-6057G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721579 | ||||||
chrX:37721588
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.509-6048A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721588 | ||||||
chrX:37721669
|
G | A | 1 | a0001c0002t0020g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-5967G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721669 | ||||||
chrX:37721984
|
C | G | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-5652C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37721984 | ||||||
chrX:37722117
|
G | A | 1 | a0001c0002t0020g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.509-5519G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722117 | ||||||
chrX:37722153
|
A | G | 3 | a0001c0001t0008g0125a0001c0001t0008g0126a0001c0001t0008g0127 | 3 | HG02970.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.509-5483A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722153 | ||||||
chrX:37722204
|
T | G | 1 | a0001c0001t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.509-5432T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722204 | ||||||
chrX:37722433
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-5203G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722433 | ||||||
chrX:37722455
|
G | A | 4 | a0001c0001t0003g0170a0001c0001t0009g0128a0001c0001t0009g0169others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-5181G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722455 | ||||||
chrX:37722490
|
A | T | 2 | a0001c0001t0001g0146a0001c0001t0016g0108 | 2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.509-5146A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722490 | ||||||
chrX:37722786
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG00609.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.509-4850T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37722786 | ||||||
chrX:37723467
|
A | G | 72 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(69): Show | 82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-4169A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723467 | ||||||
chrX:37723708
|
A | G | 10 | a0001c0001t0003g0011a0001c0001t0003g0035a0001c0001t0003g0036others(7): Show | 11 | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-3928A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723708 | ||||||
chrX:37723774
|
C | T | 2 | a0001c0001t0003g0137a0001c0001t0003g0138 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509-3862C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723774 | ||||||
chrX:37723934
|
A | C | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509-3702A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37723934 | ||||||
chrX:37724231
|
G | A | 3 | a0001c0001t0013g0172a0001c0001t0013g0174a0001c0001t0021g0173 | 3 | HG01255.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509-3405G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724231 | ||||||
chrX:37724273
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0086 | 3 | HG00140.hp1 HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.509-3363G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724273 | ||||||
chrX:37724375
|
T | G | 72 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0002g0131others(69): Show | 82 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.509-3261T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37724375 | ||||||
chrX:37724822
|
T | TA | 1 | a0001c0001t0001g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.509-2803dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37724822 | |||||
chrX:37725124
|
C | G | 1 | a0001c0003t0010g0017 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-2512C>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725124 | ||||||
chrX:37725568
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.509-2068C>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725568 | ||||||
chrX:37725588
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0044a0001c0001t0001g0045others(9): Show | 13 | HG01123.hp2 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.509-2048A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725588 | ||||||
chrX:37725596
|
G | T | 4 | a0001c0001t0003g0170a0001c0001t0009g0128a0001c0001t0009g0169others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-2040G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37725596 | ||||||
chrX:37726217
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1419G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726217 | ||||||
chrX:37726218
|
T | G | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1418T>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726218 | ||||||
chrX:37726219
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1417G>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726219 | ||||||
chrX:37726287
|
T | TA | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1343dupA | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726287 | |||||
chrX:37726297
|
A | C | 1 | a0001c0001t0003g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.509-1339A>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726297 | ||||||
chrX:37726332
|
AT | A | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1299delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726332 | |||||
chrX:37726382
|
TG | T | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1251delG | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726382 | |||||
chrX:37726409
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.509-1227T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726409 | ||||||
chrX:37726458
|
A | T | 4 | a0001c0001t0003g0170a0001c0001t0009g0128a0001c0001t0009g0169others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1178A>T | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726458 | ||||||
chrX:37726477
|
CAT | C | 1 | a0001c0002t0005g0142 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.509-1157_509-1156d others(4): Show |
XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726477 | |||||
chrX:37726553
|
GT | G | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-1079delT | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726553 | |||||
chrX:37726674
|
T | TC | 1 | a0001c0001t0001g0046 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.509-958dupC | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 37726674 | |||||
chrX:37726686
|
T | C | 1 | a0001c0001t0002g0160 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.509-950T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726686 | ||||||
chrX:37726928
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.509-708T>C | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37726928 | ||||||
chrX:37727058
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.509-578A>G | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37727058 | ||||||
chrX:37727256
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.509-380G>A | XK | ENSG00000047597.7 | transcript | ENST00000378616.5 | protein_coding | 2/2 | chrX | 37727256 |