geneid | 2710 |
---|---|
ensemblid | ENSG00000198814.14 |
hgncid | 4289 |
symbol | GK |
name | glycerol kinase |
refseq_nuc | NM_001205019.2 |
refseq_prot | NP_001191948.1 |
ensembl_nuc | ENST00000427190.6 |
ensembl_prot | ENSP00000401720.2 |
mane_status | MANE Select |
chr | chrX |
start | 30653423 |
end | 30731462 |
strand | + |
ver | v1.2 |
region | chrX:30653423-30731462 |
region5000 | chrX:30648423-30736462 |
regionname0 | GK_chrX_30653423_30731462 |
regionname5000 | GK_chrX_30648423_30736462 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 286 | 72 | 55 | 118 | 11 | 28 | 89 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1680 | 279 | 69 | 51 | 118 | 11 | 28 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
c0002 | 0/0 | 1680 | 4 | 0 | 4 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
c0003 | 0/0 | 1680 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
c0004 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2835 | 91 | 11 | 16 | 47 | 2 | 14 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0002 | 0/0 | 2836 | 85 | 14 | 19 | 37 | 6 | 9 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0003 | 1/0 | 2836 | 68 | 16 | 16 | 29 | 3 | 3 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0004 | 0/0 | 2836 | 10 | 10 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0005 | 0/0 | 2835 | 6 | 6 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0006 | 0/0 | 2836 | 3 | 0 | 3 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0007 | 0/0 | 2835 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0008 | 0/0 | 2835 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0009 | 0/0 | 2835 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0010 | 0/0 | 2835 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0011 | 0/0 | 2837 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0012 | 0/0 | 2836 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0013 | 0/0 | 2835 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0014 | 0/0 | 2836 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0015 | 0/0 | 2836 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0016 | 0/0 | 2836 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0017 | 0/0 | 2836 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0018 | 0/0 | 2836 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0019 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0020 | 0/0 | 2836 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0021 | 0/0 | 2836 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0022 | 0/0 | 2835 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
t0023 | 0/0 | 2836 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1680 | 279 | 69 | 51 | 118 | 11 | 28 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0002 | 0/0 | 1680 | 4 | 0 | 4 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0003 | 0/0 | 1680 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0004 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4514 | 91 | 11 | 16 | 47 | 2 | 14 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0002 | 0/0 | 4515 | 85 | 14 | 19 | 37 | 6 | 9 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0003 | 1/0 | 4515 | 66 | 14 | 16 | 29 | 3 | 3 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0004 | 0/0 | 4515 | 10 | 10 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0005 | 0/0 | 4514 | 6 | 6 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0007 | 0/0 | 4514 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0008 | 0/0 | 4514 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0009 | 0/0 | 4514 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0010 | 0/0 | 4514 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0011 | 0/0 | 4516 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0012 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0013 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0014 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0015 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0016 | 0/0 | 4515 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0018 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0019 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0021 | 0/0 | 4515 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0022 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0001t0023 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0002t0006 | 0/0 | 4515 | 3 | 0 | 3 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0002t0020 | 0/0 | 4515 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0003t0003 | 0/0 | 4515 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
a0001c0004t0017 | 0/0 | 4515 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | copy fasta | chrX | 30648423 | 30736462 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0003g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0016g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0021g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0022g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0001t0023g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0002t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0002t0020g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
a0001c0004t0017g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0218 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0119 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | FIN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00741 | hp1 | a0001 | c0002 | t0020 | g0189 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01099 | hp1 | a0001 | c0002 | t0006 | g0186 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01168 | hp1 | a0001 | c0002 | t0006 | g0187 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0255 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01884 | hp1 | a0001 | c0004 | t0017 | g0111 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0101 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01981 | hp1 | a0001 | c0002 | t0006 | g0188 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0115 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02135 | hp1 | a0001 | c0001 | t0018 | g0159 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0167 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0165 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02818 | hp2 | a0001 | c0001 | t0015 | g0106 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0153 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0164 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03195 | hp1 | a0001 | c0001 | t0023 | g0173 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0170 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0185 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0110 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | ESN | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | GWD | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03704 | hp1 | a0001 | c0001 | t0016 | g0272 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03710 | hp1 | a0001 | c0001 | t0022 | g0040 | SAS | PJL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | CHB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19001 | hp2 | a0001 | c0001 | t0019 | g0112 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19079 | hp1 | a0001 | c0001 | t0021 | g0222 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ASW | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ASW | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | TSI | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | USA | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | USA | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0181 | AFR | LWK | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0050 | REF | REF | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0228 | REF | REF | GK_chrX_30648423_30736462 | GK | chrX | 30648423 | 30736462 |
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:30668024
|
G | A | 1 | a0001c0002 | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
synonymous_variant | LOW | c.165G>A | p.Gln55Gln | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/21 | 280/4515 | 165/1680 | 55/559 | chrX | 30668024 | ||
chrX:30668045
|
T | C | 1 | a0001c0004 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.186T>C | p.His62His | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/21 | 301/4515 | 186/1680 | 62/559 | chrX | 30668045 | ||
chrX:30694486
|
C | T | 1 | a0001c0003 | 2 | HG02145.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.501C>T | p.Ala167Ala | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/21 | 616/4515 | 501/1680 | 167/559 | chrX | 30694486 |
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:30728932
|
A | T | 1 | a0001c0001t0023 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 190 | chrX | 30728932 | |||||
chrX:30728939
|
G | T | 1 | a0001c0001t0022 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 197 | chrX | 30728939 | |||||
chrX:30728942
|
GT | G | 7 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(4): Show | 105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*214delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 214 | INFO_REALIGN_3_PRIME | chrX | 30728942 | ||||
chrX:30728968
|
GT | G | 1 | a0001c0001t0010 | 2 | HG02976.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 228 | INFO_REALIGN_3_PRIME | chrX | 30728968 | ||||
chrX:30728982
|
A | C | 1 | a0001c0001t0021 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 240 | chrX | 30728982 | |||||
chrX:30729082
|
C | T | 2 | a0001c0002t0006a0001c0002t0020 | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*340C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 340 | chrX | 30729082 | |||||
chrX:30729706
|
T | C | 1 | a0001c0001t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*964T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 964 | chrX | 30729706 | |||||
chrX:30729739
|
C | A | 3 | a0001c0001t0005a0001c0001t0007a0001c0001t0008 | 10 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*997C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 997 | chrX | 30729739 | |||||
chrX:30729924
|
A | C | 1 | a0001c0001t0012 | 2 | HG03098.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1182A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1182 | chrX | 30729924 | |||||
chrX:30729986
|
T | C | 1 | a0001c0001t0014 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1244T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1244 | chrX | 30729986 | |||||
chrX:30730154
|
A | G | 1 | a0001c0001t0008 | 2 | HG01891.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1412A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1412 | chrX | 30730154 | |||||
chrX:30730167
|
T | C | 11 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1425T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1425 | chrX | 30730167 | |||||
chrX:30730358
|
C | A | 1 | a0001c0001t0015 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1616C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1616 | chrX | 30730358 | |||||
chrX:30730641
|
T | C | 1 | a0001c0004t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 1899 | chrX | 30730641 | |||||
chrX:30730791
|
T | TA | 1 | a0001c0001t0011 | 2 | HG02258.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2062dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2063 | INFO_REALIGN_3_PRIME | chrX | 30730791 | ||||
chrX:30730791
|
TA | T | 1 | a0001c0001t0019 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2062delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2062 | INFO_REALIGN_3_PRIME | chrX | 30730791 | ||||
chrX:30730870
|
A | G | 1 | a0001c0001t0018 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2128A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2128 | chrX | 30730870 | |||||
chrX:30730934
|
C | A | 1 | a0001c0001t0007 | 2 | HG02109.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2192C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2192 | chrX | 30730934 | |||||
chrX:30730964
|
T | C | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2222T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2222 | chrX | 30730964 | |||||
chrX:30730966
|
T | C | 1 | a0001c0002t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2224T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2224 | chrX | 30730966 | |||||
chrX:30731025
|
T | G | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2283T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2283 | chrX | 30731025 | |||||
chrX:30731330
|
T | A | 1 | a0001c0001t0016 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 21/21 | 2588 | chrX | 30731330 |
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:30653779
|
G | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(200): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.78+164G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30653779 | ||||||
chrX:30654004
|
G | A | 8 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+389G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654004 | ||||||
chrX:30654017
|
T | TG | 1 | a0001c0001t0001g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.78+408dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30654017 | |||||
chrX:30654069
|
C | T | 1 | a0001c0001t0005g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+454C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654069 | ||||||
chrX:30654390
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.78+775T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654390 | ||||||
chrX:30654610
|
T | A | 1 | a0001c0001t0001g0015 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.78+995T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654610 | ||||||
chrX:30654624
|
G | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78+1009G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654624 | ||||||
chrX:30654703
|
A | T | 1 | a0001c0001t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.78+1088A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654703 | ||||||
chrX:30654983
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.78+1368T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30654983 | ||||||
chrX:30655253
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.78+1638G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655253 | ||||||
chrX:30655374
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0278 | 2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.78+1759A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655374 | ||||||
chrX:30655400
|
A | AG | 15 | a0001c0001t0001g0017a0001c0001t0001g0190a0001c0001t0001g0191others(12): Show | 15 | HG00597.hp1 HG01346.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.78+1790dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30655400 | |||||
chrX:30655752
|
A | G | 28 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(25): Show | 28 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.78+2137A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655752 | ||||||
chrX:30655981
|
A | G | 1 | a0001c0003t0003g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.78+2366A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30655981 | ||||||
chrX:30656003
|
A | G | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.78+2388A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656003 | ||||||
chrX:30656115
|
G | GT | 1 | a0001c0001t0001g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.78+2506dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30656115 | |||||
chrX:30656143
|
A | G | 92 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0168others(89): Show | 95 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.78+2528A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656143 | ||||||
chrX:30656335
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0109 | 3 | HG02647.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.78+2720A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656335 | ||||||
chrX:30656526
|
G | A | 1 | a0001c0001t0012g0110 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78+2911G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656526 | ||||||
chrX:30656543
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+2928T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656543 | ||||||
chrX:30656587
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.78+2972G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656587 | ||||||
chrX:30656599
|
T | TC | 1 | a0001c0001t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.78+2992dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30656599 | |||||
chrX:30656606
|
C | G | 1 | a0001c0001t0005g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.78+2991C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656606 | ||||||
chrX:30656606
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+2991C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656606 | ||||||
chrX:30656607
|
C | G | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.78+2992C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656607 | ||||||
chrX:30656895
|
G | T | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78+3280G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30656895 | ||||||
chrX:30657129
|
G | T | 1 | a0001c0001t0016g0272 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.78+3514G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657129 | ||||||
chrX:30657268
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.78+3653T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657268 | ||||||
chrX:30657308
|
T | A | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.78+3693T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657308 | ||||||
chrX:30657417
|
A | T | 2 | a0001c0001t0002g0183a0001c0001t0004g0184 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78+3802A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657417 | ||||||
chrX:30657676
|
G | T | 1 | a0001c0001t0004g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.78+4061G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657676 | ||||||
chrX:30657703
|
AGTAACTG | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78+4091_78+4097del others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30657703 | |||||
chrX:30657908
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.78+4293A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657908 | ||||||
chrX:30657972
|
T | C | 1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.78+4357T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30657972 | ||||||
chrX:30658051
|
C | T | 13 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0005g0022others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+4436C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658051 | ||||||
chrX:30658319
|
G | GT | 3 | a0001c0001t0003g0166a0001c0001t0005g0107a0001c0004t0017g0111 | 3 | HG01884.hp1 HG02523.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.78+4716dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30658319 | |||||
chrX:30658325
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+4710T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658325 | ||||||
chrX:30658396
|
C | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+4781C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658396 | ||||||
chrX:30658402
|
G | A | 7 | a0001c0001t0004g0172a0001c0001t0004g0174a0001c0001t0004g0175others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+4787G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658402 | ||||||
chrX:30658507
|
G | A | 57 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(54): Show | 60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.78+4892G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658507 | ||||||
chrX:30658541
|
ATCCTGAC others(1424): Show |
A | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+4938_79-5528del | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30658541 | |||||
chrX:30658697
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.78+5082G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658697 | ||||||
chrX:30658791
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.78+5176T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658791 | ||||||
chrX:30658903
|
T | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.78+5288T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30658903 | ||||||
chrX:30659034
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+5419C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659034 | ||||||
chrX:30659060
|
CTCT | C | 1 | a0001c0001t0002g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.78+5450_78+5452del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30659060 | |||||
chrX:30659069
|
T | A | 1 | a0001c0001t0002g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.78+5454T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659069 | ||||||
chrX:30659554
|
A | G | 1 | a0001c0002t0020g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.78+5939A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659554 | ||||||
chrX:30659570
|
G | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-5941G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659570 | ||||||
chrX:30659615
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.79-5896G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659615 | ||||||
chrX:30659686
|
G | A | 2 | a0001c0001t0002g0183a0001c0001t0004g0184 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.79-5825G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659686 | ||||||
chrX:30659705
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-5806C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659705 | ||||||
chrX:30659892
|
GTGT | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-5618_79-5616del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659892 | ||||||
chrX:30659897
|
C | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-5614C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659897 | ||||||
chrX:30659899
|
C | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-5612C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30659899 | ||||||
chrX:30660136
|
C | T | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-5375C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660136 | ||||||
chrX:30660198
|
G | GTAA | 5 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(2): Show | 5 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-5291_79-5289dup others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660198 | |||||
chrX:30660198
|
G | GTAATAA | 1 | a0001c0001t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79-5294_79-5289dup others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660198 | |||||
chrX:30660198
|
GTAA | G | 56 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(53): Show | 59 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.79-5291_79-5289del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660198 | |||||
chrX:30660252
|
T | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0030others(1): Show | 4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5259T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660252 | ||||||
chrX:30660461
|
A | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5050A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660461 | ||||||
chrX:30660514
|
C | CA | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.79-4996dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660514 | |||||
chrX:30660792
|
A | AT | 13 | a0001c0001t0002g0271a0001c0001t0003g0008a0001c0001t0003g0009others(10): Show | 13 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-4707dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660792 | |||||
chrX:30660792
|
AT | A | 9 | a0001c0001t0001g0032a0001c0001t0002g0209a0001c0001t0004g0171others(6): Show | 9 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-4707delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660792 | |||||
chrX:30660812
|
C | CT | 7 | a0001c0001t0001g0090a0001c0001t0001g0201a0001c0001t0002g0268others(4): Show | 7 | HG01346.hp2 HG02148.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-4682dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660812 | |||||
chrX:30660812
|
CT | C | 91 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0146others(88): Show | 94 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.79-4682delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30660812 | |||||
chrX:30660844
|
C | T | 1 | a0001c0001t0015g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-4667C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660844 | ||||||
chrX:30660869
|
G | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-4642G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30660869 | ||||||
chrX:30661012
|
C | T | 12 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-4499C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661012 | ||||||
chrX:30661079
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79-4432T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661079 | ||||||
chrX:30661087
|
T | C | 89 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0183others(86): Show | 92 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.79-4424T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661087 | ||||||
chrX:30661511
|
TCAA | T | 59 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(56): Show | 62 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.79-3996_79-3994del others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30661511 | |||||
chrX:30661533
|
GC | G | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.79-3975delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30661533 | |||||
chrX:30661789
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-3722C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661789 | ||||||
chrX:30661880
|
GA | G | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.79-3625delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30661880 | |||||
chrX:30661971
|
T | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-3540T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30661971 | ||||||
chrX:30662047
|
G | GA | 1 | a0001c0001t0002g0212 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.79-3458dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662047 | |||||
chrX:30662111
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-3400A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662111 | ||||||
chrX:30662163
|
C | CCAGATTT | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(199): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.79-3346_79-3345ins others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662163 | |||||
chrX:30662431
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-3080G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662431 | ||||||
chrX:30662492
|
CA | C | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.79-3015delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662492 | |||||
chrX:30662695
|
C | T | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2816C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662695 | ||||||
chrX:30662703
|
T | C | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2808T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662703 | ||||||
chrX:30662707
|
C | T | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2804C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662707 | ||||||
chrX:30662709
|
T | C | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2802T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662709 | ||||||
chrX:30662709
|
T | TTTTC | 52 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(49): Show | 54 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-2777_79-2774dup others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | |||||
chrX:30662709
|
T | TTTTCTTT others(1): Show |
9 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0084others(6): Show | 9 | HG00544.hp1 HG01175.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-2781_79-2774dup others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | |||||
chrX:30662709
|
T | TTTTCTTT others(9): Show |
1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.79-2789_79-2774dup others(16): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | |||||
chrX:30662709
|
TTTTC | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0213others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-2777_79-2774del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | |||||
chrX:30662709
|
TTTTCTTT others(1): Show |
T | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02015.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-2781_79-2774del others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662709 | |||||
chrX:30662711
|
T | C | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2800T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662711 | ||||||
chrX:30662713
|
C | T | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.79-2798C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662713 | ||||||
chrX:30662738
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0004g0172a0001c0001t0008g0165 | 3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2773C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662738 | ||||||
chrX:30662742
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0004g0172a0001c0001t0008g0165 | 3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2769T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662742 | ||||||
chrX:30662746
|
TTTCC | T | 83 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0183others(80): Show | 86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.79-2745_79-2742del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662746 | |||||
chrX:30662750
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0004g0172a0001c0001t0008g0165 | 3 | HG02622.hp1 HG02809.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-2761C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662750 | ||||||
chrX:30662761
|
CCTTCCT | C | 1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-2749_79-2744del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662761 | ||||||
chrX:30662763
|
TTCCTTC | T | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.79-2745_79-2740del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662763 | |||||
chrX:30662767
|
T | TTC | 12 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(9): Show | 12 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-2724_79-2723dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | |||||
chrX:30662767
|
TTC | T | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0021others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-2724_79-2723del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | |||||
chrX:30662767
|
TTCTC | T | 3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0016g0272 | 3 | HG02015.hp1 HG03704.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.79-2726_79-2723del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662767 | |||||
chrX:30662769
|
C | CCT | 1 | a0001c0001t0001g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.79-2742_79-2741ins others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662769 | ||||||
chrX:30662789
|
T | C | 2 | a0001c0001t0004g0171a0001c0001t0004g0180 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.79-2722T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662789 | ||||||
chrX:30662792
|
T | C | 1 | a0001c0001t0011g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-2719T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662792 | ||||||
chrX:30662807
|
CCT | C | 1 | a0001c0001t0011g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-2703_79-2702del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662807 | ||||||
chrX:30662808
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2703C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662808 | ||||||
chrX:30662809
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2702T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662809 | ||||||
chrX:30662809
|
T | TCTC | 1 | a0001c0001t0019g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.79-2702_79-2701ins others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662809 | ||||||
chrX:30662809
|
T | TTC | 4 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0268others(1): Show | 4 | HG00408.hp2 HG01433.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2678_79-2677dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | |||||
chrX:30662809
|
T | TTCTCTCT others(3): Show |
1 | a0001c0002t0006g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.79-2686_79-2677dup others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | |||||
chrX:30662809
|
TTC | T | 3 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009 | 3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-2678_79-2677del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662809 | |||||
chrX:30662825
|
CTCTCTCT others(35): Show |
C | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.79-2680_79-2639del others(42): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662825 | |||||
chrX:30662827
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2684C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662827 | ||||||
chrX:30662829
|
CTCTCTT | C | 2 | a0001c0001t0003g0179a0001c0001t0011g0007 | 2 | HG02258.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.79-2678_79-2673del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662829
|
CTCTCTTT others(3): Show |
C | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.79-2678_79-2669del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662829
|
CTCTCTTT others(7): Show |
C | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79-2678_79-2665del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662829
|
CTCTCTTT others(11): Show |
C | 4 | a0001c0001t0003g0012a0001c0001t0003g0162a0001c0001t0003g0163others(1): Show | 4 | HG01361.hp1 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2678_79-2661del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662829
|
CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0001g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.79-2678_79-2653del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662829
|
CTCTCTTT others(31): Show |
C | 1 | a0001c0001t0012g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79-2654_79-2617del others(38): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662829 | |||||
chrX:30662831
|
C | CTCTCT | 1 | a0001c0002t0006g0187 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.79-2677_79-2676ins others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | |||||
chrX:30662831
|
C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0213 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.79-2677_79-2676ins others(11): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | |||||
chrX:30662831
|
C | CTCTCTT | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.79-2677_79-2676ins others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | |||||
chrX:30662831
|
C | CTCTTCTT | 3 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0227 | 3 | HG02027.hp1 HG02129.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.79-2676_79-2675ins others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | |||||
chrX:30662831
|
C | CTT | 2 | a0001c0001t0002g0271a0001c0001t0003g0178 | 2 | HG02818.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.79-2679_79-2678ins others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662831 | |||||
chrX:30662831
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0002g0168a0001c0001t0012g0110others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2680C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662831 | ||||||
chrX:30662833
|
CTTTCTT | C | 4 | a0001c0001t0002g0021a0001c0001t0003g0120a0001c0001t0003g0121others(1): Show | 4 | HG00609.hp1 HG01106.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2671del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662833
|
CTTTCTTT others(3): Show |
C | 4 | a0001c0001t0003g0113a0001c0001t0003g0123a0001c0001t0003g0124others(1): Show | 4 | HG01192.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2667del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662833
|
CTTTCTTT others(7): Show |
C | 35 | a0001c0001t0001g0019a0001c0001t0002g0146a0001c0001t0003g0002others(32): Show | 38 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-2676_79-2663del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662833
|
CTTTCTTT others(11): Show |
C | 8 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0055others(5): Show | 8 | HG01074.hp1 HG01175.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-2676_79-2659del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662833
|
CTTTCTTT others(15): Show |
C | 13 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0050others(10): Show | 13 | HG01167.hp1 HG01358.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-2676_79-2655del others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662833
|
CTTTCTTT others(19): Show |
C | 4 | a0001c0001t0004g0174a0001c0001t0004g0177a0001c0001t0005g0022others(1): Show | 4 | HG02886.hp2 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2676_79-2651del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662833 | |||||
chrX:30662834
|
T | TC | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.79-2677_79-2676ins others(1): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662834 | ||||||
chrX:30662835
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.79-2676T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662835 | ||||||
chrX:30662837
|
CT | C | 1 | a0001c0001t0001g0036 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.79-2671delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662837 | |||||
chrX:30662839
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0005g0100a0001c0001t0013g0023 | 3 | HG02615.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.79-2672T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662839 | ||||||
chrX:30662839
|
TTCTTTCT others(23): Show |
T | 5 | a0001c0001t0001g0054a0001c0001t0001g0200a0001c0001t0004g0171others(2): Show | 5 | HG00597.hp1 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-2646_79-2617del others(30): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662839 | |||||
chrX:30662842
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2669T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662842 | ||||||
chrX:30662843
|
TTCTTTCT others(19): Show |
T | 11 | a0001c0001t0001g0032a0001c0001t0001g0051a0001c0001t0001g0052others(8): Show | 11 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-2642_79-2617del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662843 | |||||
chrX:30662847
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.79-2664T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662847 | ||||||
chrX:30662847
|
TTCTTTCT others(15): Show |
T | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(71): Show | 77 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.79-2640_79-2619del others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662847 | |||||
chrX:30662851
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79-2660T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662851 | ||||||
chrX:30662851
|
TTCTTTCT others(11): Show |
T | 10 | a0001c0001t0002g0095a0001c0001t0002g0168a0001c0001t0002g0267others(7): Show | 10 | HG00099.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-2640_79-2623del others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662851 | |||||
chrX:30662855
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0055 | 2 | HG03834.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.79-2656T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662855 | ||||||
chrX:30662855
|
TTCTTTCT others(7): Show |
T | 17 | a0001c0001t0001g0018a0001c0001t0002g0091a0001c0001t0002g0092others(14): Show | 17 | HG00558.hp1 HG00642.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-2640_79-2627del others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662855 | |||||
chrX:30662859
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79-2652T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662859 | ||||||
chrX:30662859
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0265a0001c0001t0003g0013 | 2 | HG02280.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.79-2640_79-2631del others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662859 | |||||
chrX:30662863
|
TTCTTTC | T | 8 | a0001c0001t0002g0208a0001c0001t0002g0260a0001c0001t0002g0261others(5): Show | 8 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-2640_79-2635del others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662863 | |||||
chrX:30662867
|
TTC | T | 101 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(98): Show | 104 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.79-2640_79-2639del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662867 | |||||
chrX:30662869
|
C | CTT | 24 | a0001c0001t0001g0213a0001c0001t0002g0210a0001c0001t0002g0216others(21): Show | 24 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | CTTTCTT | 13 | a0001c0001t0002g0005a0001c0001t0002g0214a0001c0001t0002g0233others(10): Show | 14 | HG00544.hp2 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | CTTTCTTT others(3): Show |
7 | a0001c0001t0002g0205a0001c0001t0002g0212a0001c0001t0002g0230others(4): Show | 7 | HG00741.hp1 HG02040.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | CTTTCTTT others(7): Show |
1 | a0001c0002t0006g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.79-2641_79-2640ins others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | CTTTCTTT others(11): Show |
2 | a0001c0001t0002g0211a0001c0001t0002g0215 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.79-2641_79-2640ins others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | CTTTCTTT others(91): Show |
1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-2641_79-2640ins others(98): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662869 | |||||
chrX:30662869
|
C | T | 1 | a0001c0001t0012g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79-2642C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662869 | ||||||
chrX:30662880
|
T | TTC | 1 | a0001c0001t0002g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.79-2630_79-2629ins others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662880 | |||||
chrX:30662891
|
CT | C | 1 | a0001c0001t0003g0006 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-2616delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30662891 | |||||
chrX:30662944
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2567G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30662944 | ||||||
chrX:30663023
|
C | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-2488C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663023 | ||||||
chrX:30663255
|
CA | C | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-2255delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663255 | ||||||
chrX:30663296
|
AG | A | 1 | a0001c0001t0002g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.79-2214delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663296 | ||||||
chrX:30663374
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79-2137T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663374 | ||||||
chrX:30663384
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79-2127G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663384 | ||||||
chrX:30663525
|
G | C | 1 | a0001c0001t0002g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.79-1986G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663525 | ||||||
chrX:30663579
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-1932G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663579 | ||||||
chrX:30663591
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79-1920A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663591 | ||||||
chrX:30663663
|
A | AG | 1 | a0001c0001t0002g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.79-1843dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663663 | |||||
chrX:30663923
|
G | GCT | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1575_79-1574dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663923 | |||||
chrX:30663964
|
T | TATATATA others(29): Show |
84 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(65): Show |
2 | a0001c0001t0005g0105a0001c0001t0005g0107 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(65): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0194others(6): Show | 9 | HG01934.hp1 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-1517_79-1516ins others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(171): Show |
1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-1480_79-1479ins others(178): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(65): Show |
1 | a0001c0001t0002g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79-1458_79-1387dup others(72): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(278): Show |
1 | a0001c0001t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(207): Show |
5 | a0001c0001t0002g0214a0001c0001t0002g0225a0001c0001t0002g0229others(2): Show | 5 | HG01346.hp2 HG02004.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(214): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(243): Show |
46 | a0001c0001t0001g0265a0001c0001t0002g0005a0001c0001t0002g0205others(43): Show | 47 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(250): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(279): Show |
16 | a0001c0001t0001g0213a0001c0001t0002g0209a0001c0001t0002g0215others(13): Show | 16 | HG00099.hp1 HG00423.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.79-1444_79-1443ins others(286): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(208): Show |
1 | a0001c0001t0002g0232 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(215): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(101): Show |
1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.79-1494_79-1387dup others(108): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(278): Show |
2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.79-1408_79-1407ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(279): Show |
1 | a0001c0001t0002g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(286): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(137): Show |
2 | a0001c0001t0002g0091a0001c0001t0002g0095 | 2 | HG02293.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.79-1530_79-1387dup others(144): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(173): Show |
1 | a0001c0001t0002g0092 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(180): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATA others(209): Show |
2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(216): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663964
|
T | TATATATT others(29): Show |
1 | a0001c0001t0001g0003 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.79-1541_79-1540ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30663964 | |||||
chrX:30663982
|
A | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1529A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663982 | ||||||
chrX:30663995
|
T | G | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-1516T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30663995 | ||||||
chrX:30664000
|
G | GATATATA others(86): Show |
1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-1445_79-1444ins others(93): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664000 | |||||
chrX:30664015
|
T | G | 1 | a0001c0003t0003g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.79-1496T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664015 | ||||||
chrX:30664028
|
AT | A | 15 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(12): Show | 15 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-1479delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664028 | |||||
chrX:30664031
|
T | TTATAGAT others(183): Show |
1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(190): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664031 | |||||
chrX:30664053
|
T | TATCTATA others(278): Show |
1 | a0001c0001t0016g0272 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.79-1444_79-1443ins others(285): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664053 | |||||
chrX:30664064
|
ATTTTATA others(30): Show |
A | 1 | a0001c0001t0003g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.79-1443_79-1407del others(37): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664064 | |||||
chrX:30664065
|
T | TTTTATAG others(28): Show |
7 | a0001c0001t0005g0100a0001c0001t0005g0203a0001c0001t0007g0102others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-1442_79-1408dup others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664065 | |||||
chrX:30664089
|
T | G | 9 | a0001c0001t0001g0213a0001c0001t0002g0205a0001c0001t0002g0212others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-1422T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664089 | ||||||
chrX:30664089
|
TATCTATA others(29): Show |
T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1383_79-1348del others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664089 | |||||
chrX:30664090
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-1421A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664090 | ||||||
chrX:30664100
|
AT | A | 69 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(66): Show | 72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.79-1407delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664100 | |||||
chrX:30664101
|
T | TTTATAGA others(27): Show |
1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(34): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | |||||
chrX:30664101
|
T | TTTATAGA others(63): Show |
1 | a0001c0001t0004g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79-1408_79-1407ins others(70): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | |||||
chrX:30664101
|
T | TTTTATAG others(28): Show |
10 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(7): Show | 10 | HG01515.hp1 HG01517.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | |||||
chrX:30664101
|
T | TTTTATAG others(64): Show |
1 | a0001c0001t0003g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(71): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664101 | |||||
chrX:30664103
|
T | TTATAGAT others(173): Show |
1 | a0001c0001t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(180): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664103 | |||||
chrX:30664103
|
T | TTATAGAT others(137): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.79-1387_79-1386ins others(144): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664103 | |||||
chrX:30664108
|
G | GATATATA others(29): Show |
1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664108 | |||||
chrX:30664111
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.79-1400A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664111 | ||||||
chrX:30664119
|
T | TATATATA others(28): Show |
1 | a0001c0001t0011g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79-1387_79-1386ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664119 | |||||
chrX:30664125
|
G | GATATATA others(28): Show |
1 | a0001c0001t0003g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79-1384_79-1383ins others(35): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664125 | |||||
chrX:30664125
|
G | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.79-1386G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664125 | ||||||
chrX:30664128
|
C | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79-1383C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664128 | ||||||
chrX:30664128
|
CTA | C | 1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.79-1375_79-1374del others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664128 | |||||
chrX:30664199
|
A | AT | 3 | a0001c0001t0002g0223a0001c0001t0003g0152a0001c0001t0019g0112 | 3 | HG01433.hp1 HG01978.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.79-1299dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664199 | |||||
chrX:30664702
|
C | CT | 56 | a0001c0001t0002g0155a0001c0001t0002g0168a0001c0001t0002g0205others(53): Show | 58 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.79-787dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | |||||
chrX:30664702
|
C | CTT | 30 | a0001c0001t0002g0146a0001c0001t0002g0212a0001c0001t0003g0004others(27): Show | 31 | HG00609.hp1 HG00642.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.79-788_79-787dupTT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | |||||
chrX:30664702
|
C | CTTT | 2 | a0001c0001t0003g0151a0001c0001t0019g0112 | 2 | HG00408.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.79-789_79-787dupTT others(1): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | |||||
chrX:30664702
|
CT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(89): Show | 95 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.79-787delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | |||||
chrX:30664702
|
CTT | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG03490.hp1 HG03704.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-788_79-787delTT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 30664702 | |||||
chrX:30664860
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79-651C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30664860 | ||||||
chrX:30665035
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.79-476G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665035 | ||||||
chrX:30665071
|
C | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-440C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665071 | ||||||
chrX:30665337
|
T | A | 1 | a0001c0001t0002g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.79-174T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 1/20 | chrX | 30665337 | ||||||
chrX:30665613
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152+29C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665613 | ||||||
chrX:30665620
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0003g0137 | 2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.152+36T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665620 | ||||||
chrX:30665681
|
A | G | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+97A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665681 | ||||||
chrX:30665833
|
G | C | 8 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+249G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30665833 | ||||||
chrX:30665904
|
TTGAG | T | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+323_152+326del others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 30665904 | |||||
chrX:30666047
|
TA | T | 1 | a0001c0001t0002g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.152+467delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 30666047 | |||||
chrX:30666157
|
GA | G | 1 | a0001c0001t0002g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.152+575delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 30666157 | |||||
chrX:30666178
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.152+594G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666178 | ||||||
chrX:30666191
|
A | G | 10 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0237others(7): Show | 10 | HG00597.hp2 NA18612.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+607A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666191 | ||||||
chrX:30666222
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+638G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666222 | ||||||
chrX:30666236
|
AC | A | 1 | a0001c0001t0002g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.152+654delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 30666236 | |||||
chrX:30666325
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+741C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666325 | ||||||
chrX:30666593
|
C | T | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+1009C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666593 | ||||||
chrX:30666654
|
T | C | 62 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0273others(59): Show | 65 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.152+1070T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666654 | ||||||
chrX:30666970
|
T | C | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.153-1042T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30666970 | ||||||
chrX:30667029
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-983C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667029 | ||||||
chrX:30667108
|
T | C | 2 | a0001c0001t0003g0138a0001c0001t0003g0139 | 2 | NA18993.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.153-904T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667108 | ||||||
chrX:30667118
|
C | T | 2 | a0001c0001t0005g0203a0001c0001t0015g0106 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.153-894C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667118 | ||||||
chrX:30667177
|
TA | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153-826delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 30667177 | |||||
chrX:30667238
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.153-774C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667238 | ||||||
chrX:30667402
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-610C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667402 | ||||||
chrX:30667709
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-303G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667709 | ||||||
chrX:30667920
|
A | C | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-92A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 2/20 | chrX | 30667920 | ||||||
chrX:30668607
|
A | G | 64 | a0001c0001t0001g0169a0001c0001t0002g0146a0001c0001t0002g0155others(61): Show | 67 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.259+489A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668607 | ||||||
chrX:30668903
|
G | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+785G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668903 | ||||||
chrX:30668942
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.259+824G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30668942 | ||||||
chrX:30669071
|
T | G | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.259+953T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669071 | ||||||
chrX:30669176
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0137 | 2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.259+1058C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669176 | ||||||
chrX:30669183
|
G | GT | 24 | a0001c0001t0001g0052a0001c0001t0001g0088a0001c0001t0002g0247others(21): Show | 24 | HG00423.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.259+1081dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30669183 | |||||
chrX:30669183
|
GT | G | 5 | a0001c0001t0001g0056a0001c0001t0001g0098a0001c0001t0001g0194others(2): Show | 5 | HG02615.hp2 HG02735.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+1081delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30669183 | |||||
chrX:30669340
|
G | T | 1 | a0001c0001t0003g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259+1222G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669340 | ||||||
chrX:30669364
|
T | C | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.259+1246T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669364 | ||||||
chrX:30669393
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259+1275A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669393 | ||||||
chrX:30669404
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259+1286G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669404 | ||||||
chrX:30669472
|
G | A | 86 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0168others(83): Show | 89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.259+1354G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669472 | ||||||
chrX:30669710
|
G | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1592G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669710 | ||||||
chrX:30669751
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.259+1633G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669751 | ||||||
chrX:30669793
|
T | TA | 1 | a0001c0001t0002g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.259+1684dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30669793 | |||||
chrX:30669859
|
G | A | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.259+1741G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30669859 | ||||||
chrX:30670115
|
C | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.259+1997C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670115 | ||||||
chrX:30670451
|
G | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(90): Show | 96 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.259+2333G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670451 | ||||||
chrX:30670598
|
A | AT | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.259+2491dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30670598 | |||||
chrX:30670598
|
AT | A | 13 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(10): Show | 13 | HG01515.hp1 HG01517.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+2491delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30670598 | |||||
chrX:30670598
|
ATT | A | 57 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(54): Show | 60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.259+2490_259+2491d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30670598 | |||||
chrX:30670850
|
G | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.259+2732G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670850 | ||||||
chrX:30670968
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.259+2850A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30670968 | ||||||
chrX:30671008
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.259+2890C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671008 | ||||||
chrX:30671135
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0201 | 2 | NA18992.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.259+3017C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671135 | ||||||
chrX:30671160
|
G | A | 8 | a0001c0001t0005g0100a0001c0001t0005g0104a0001c0001t0005g0203others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+3042G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671160 | ||||||
chrX:30671291
|
C | CA | 54 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0049others(51): Show | 54 | HG00423.hp2 HG00558.hp1 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.259+3197dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | |||||
chrX:30671291
|
C | CAA | 5 | a0001c0001t0002g0089a0001c0001t0002g0095a0001c0001t0002g0096others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3196_259+3197d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | |||||
chrX:30671291
|
C | CAAAAAAA | 1 | a0001c0001t0005g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259+3191_259+3197d others(9): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | |||||
chrX:30671291
|
CA | C | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(12): Show | 15 | HG00741.hp1 HG01515.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.259+3197delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | |||||
chrX:30671291
|
CAA | C | 3 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188 | 3 | HG01099.hp1 HG01168.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.259+3196_259+3197d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671291 | |||||
chrX:30671316
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259+3198C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671316 | ||||||
chrX:30671509
|
TTTC | T | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.259+3394_259+3396d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30671509 | |||||
chrX:30671629
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.259+3511T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30671629 | ||||||
chrX:30672062
|
G | GA | 1 | a0001c0003t0003g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.259+3946dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672062 | |||||
chrX:30672094
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+3976G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672094 | ||||||
chrX:30672159
|
C | CA | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(101): Show | 107 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.259+4066dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
C | CAA | 19 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 19 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.259+4065_259+4066d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
C | CAAA | 1 | a0001c0001t0007g0102 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.259+4064_259+4066d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
C | CAAAA | 7 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(4): Show | 7 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+4063_259+4066d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
C | CAAAAA | 3 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013 | 3 | HG02280.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.259+4062_259+4066d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
C | CAAAAAA | 2 | a0001c0001t0003g0010a0001c0001t0003g0179 | 2 | HG02622.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.259+4061_259+4066d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
CA | C | 57 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0245others(54): Show | 60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.259+4066delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672159
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0008g0101a0001c0001t0008g0165 | 2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.259+4056_259+4066d others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672159 | |||||
chrX:30672310
|
A | G | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+4192A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672310 | ||||||
chrX:30672363
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.259+4245C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672363 | ||||||
chrX:30672540
|
G | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.259+4422G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672540 | ||||||
chrX:30672727
|
T | G | 12 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(9): Show | 12 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+4609T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672727 | ||||||
chrX:30672753
|
G | T | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4622G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672753 | ||||||
chrX:30672760
|
GC | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4613delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672760 | |||||
chrX:30672814
|
C | CA | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4551dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672814 | |||||
chrX:30672919
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.260-4456T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672919 | ||||||
chrX:30672951
|
TTA | T | 6 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0085others(3): Show | 6 | HG00323.hp1 HG01175.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-4420_260-4419d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672951 | |||||
chrX:30672958
|
T | A | 4 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0223others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-4417T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30672958 | ||||||
chrX:30672958
|
T | TTA | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.260-4415_260-4414d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30672958 | |||||
chrX:30673003
|
AC | A | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4370delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30673003 | |||||
chrX:30673047
|
CT | C | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4322delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30673047 | |||||
chrX:30673168
|
G | C | 11 | a0001c0001t0002g0183a0001c0001t0003g0006a0001c0001t0003g0008others(8): Show | 11 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-4207G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673168 | ||||||
chrX:30673199
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.260-4176G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673199 | ||||||
chrX:30673235
|
C | T | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.260-4140C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673235 | ||||||
chrX:30673268
|
GA | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0278 | 2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.260-4104delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30673268 | |||||
chrX:30673284
|
A | AG | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-4089dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30673284 | |||||
chrX:30673389
|
G | A | 1 | a0001c0001t0003g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.260-3986G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673389 | ||||||
chrX:30673536
|
A | G | 60 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0273others(57): Show | 63 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.260-3839A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673536 | ||||||
chrX:30673621
|
C | T | 86 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0168others(83): Show | 89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.260-3754C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673621 | ||||||
chrX:30673649
|
T | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.260-3726T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673649 | ||||||
chrX:30673691
|
AG | A | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-3681delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30673691 | |||||
chrX:30673760
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.260-3615T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673760 | ||||||
chrX:30673945
|
A | G | 64 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0168others(61): Show | 67 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.260-3430A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30673945 | ||||||
chrX:30674077
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.260-3298T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674077 | ||||||
chrX:30674148
|
GA | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-3225delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30674148 | |||||
chrX:30674270
|
T | TG | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-3103dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30674270 | |||||
chrX:30674342
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-3033G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674342 | ||||||
chrX:30674345
|
G | GT | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-3030_260-3029i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674345 | ||||||
chrX:30674679
|
A | AAT | 1 | a0001c0001t0003g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260-2682_260-2681d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30674679 | |||||
chrX:30674681
|
T | A | 4 | a0001c0001t0001g0032a0001c0001t0002g0021a0001c0001t0009g0115others(1): Show | 4 | HG02080.hp2 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2694T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674681 | ||||||
chrX:30674729
|
GT | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2644delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30674729 | |||||
chrX:30674775
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.260-2600G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674775 | ||||||
chrX:30674778
|
AC | A | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2594delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30674778 | |||||
chrX:30674975
|
T | A | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2400T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674975 | ||||||
chrX:30674976
|
G | T | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2399G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674976 | ||||||
chrX:30674977
|
T | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2398T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30674977 | ||||||
chrX:30675012
|
GC | G | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2361delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675012 | |||||
chrX:30675021
|
A | AG | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-2352dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675021 | |||||
chrX:30675161
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.260-2214T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675161 | ||||||
chrX:30675198
|
A | AT | 19 | a0001c0001t0001g0034a0001c0001t0001g0037a0001c0001t0001g0074others(16): Show | 19 | HG00423.hp1 HG01069.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.260-2162dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675198 | |||||
chrX:30675198
|
A | ATT | 1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.260-2163_260-2162d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675198 | |||||
chrX:30675198
|
AT | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-2162delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675198 | |||||
chrX:30675265
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.260-2110G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675265 | ||||||
chrX:30675320
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-2055C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675320 | ||||||
chrX:30675341
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2034G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675341 | ||||||
chrX:30675399
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-1976G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675399 | ||||||
chrX:30675453
|
T | C | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1922T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675453 | ||||||
chrX:30675454
|
C | T | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1921C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675454 | ||||||
chrX:30675481
|
G | GC | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1892dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675481 | |||||
chrX:30675489
|
A | AC | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1883dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675489 | |||||
chrX:30675519
|
C | CT | 5 | a0001c0001t0001g0032a0001c0001t0001g0079a0001c0001t0002g0093others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-1839dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675519 | |||||
chrX:30675519
|
CT | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(18): Show | 21 | HG00323.hp1 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-1839delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675519 | |||||
chrX:30675519
|
CTT | C | 1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.260-1840_260-1839d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675519 | |||||
chrX:30675663
|
A | AC | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.260-1706dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675663 | |||||
chrX:30675725
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.260-1650C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675725 | ||||||
chrX:30675796
|
A | AT | 2 | a0001c0001t0001g0079a0001c0001t0003g0149 | 2 | HG02738.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.260-1568dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675796 | |||||
chrX:30675796
|
AT | A | 1 | a0001c0001t0001g0190 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.260-1568delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30675796 | |||||
chrX:30675816
|
G | A | 12 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(9): Show | 12 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.260-1559G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675816 | ||||||
chrX:30675880
|
C | G | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(4): Show | 7 | HG01934.hp1 NA18942.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1495C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30675880 | ||||||
chrX:30676082
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.260-1293C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676082 | ||||||
chrX:30676106
|
A | T | 1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.260-1269A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676106 | ||||||
chrX:30676118
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.260-1257A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676118 | ||||||
chrX:30676279
|
C | T | 7 | a0001c0001t0004g0172a0001c0001t0004g0174a0001c0001t0004g0175others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1096C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676279 | ||||||
chrX:30676468
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.260-907T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676468 | ||||||
chrX:30676621
|
T | C | 1 | a0001c0001t0009g0115 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.260-754T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676621 | ||||||
chrX:30676790
|
T | C | 5 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-585T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676790 | ||||||
chrX:30676879
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009 | 3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.260-496A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676879 | ||||||
chrX:30676888
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-487C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676888 | ||||||
chrX:30676943
|
G | GCA | 9 | a0001c0001t0002g0168a0001c0001t0003g0006a0001c0001t0003g0008others(6): Show | 9 | HG01515.hp1 HG01517.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.260-413_260-412dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30676943 | |||||
chrX:30676943
|
G | GCACA | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.260-415_260-412dup others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30676943 | |||||
chrX:30676948
|
C | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-427C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30676948 | ||||||
chrX:30677216
|
CACTCAAA others(6): Show |
C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.260-157_260-145del others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | 30677216 | |||||
chrX:30677247
|
A | T | 1 | a0001c0001t0003g0124 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.260-128A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 3/20 | chrX | 30677247 | ||||||
chrX:30677648
|
A | T | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337+196A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677648 | ||||||
chrX:30677655
|
T | G | 1 | a0001c0001t0003g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.337+203T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677655 | ||||||
chrX:30677806
|
G | A | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.337+354G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677806 | ||||||
chrX:30677824
|
C | CA | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(200): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.337+385dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30677824 | |||||
chrX:30677824
|
C | CAA | 2 | a0001c0001t0014g0185a0001c0001t0015g0106 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.337+384_337+385dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30677824 | |||||
chrX:30677842
|
GA | G | 2 | a0001c0001t0002g0216a0001c0001t0005g0104 | 2 | HG00323.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.337+401delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30677842 | |||||
chrX:30677844
|
A | G | 5 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+392A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677844 | ||||||
chrX:30677853
|
A | G | 5 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(2): Show | 5 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+401A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30677853 | ||||||
chrX:30678176
|
G | T | 1 | a0001c0001t0003g0179 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.337+724G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678176 | ||||||
chrX:30678632
|
T | C | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.337+1180T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678632 | ||||||
chrX:30678671
|
G | GT | 29 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 29 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.337+1233dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678671 | |||||
chrX:30678671
|
G | GTT | 1 | a0001c0001t0022g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.337+1232_337+1233d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678671 | |||||
chrX:30678671
|
GT | G | 60 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0002g0273others(57): Show | 63 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.337+1233delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678671 | |||||
chrX:30678685
|
T | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1233T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678685 | ||||||
chrX:30678695
|
G | GT | 11 | a0001c0001t0002g0262a0001c0001t0002g0267a0001c0001t0005g0100others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.337+1256dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678695 | |||||
chrX:30678695
|
GT | G | 1 | a0001c0001t0002g0232 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.337+1256delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678695 | |||||
chrX:30678701
|
T | C | 2 | a0001c0001t0003g0138a0001c0001t0003g0139 | 2 | NA18993.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.337+1249T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678701 | ||||||
chrX:30678821
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.337+1369G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678821 | ||||||
chrX:30678841
|
C | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0124a0001c0001t0003g0151 | 4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1389C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30678841 | ||||||
chrX:30678852
|
A | AT | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0043others(67): Show | 73 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.337+1419dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | |||||
chrX:30678852
|
A | ATT | 3 | a0001c0001t0003g0139a0001c0003t0003g0167a0001c0003t0003g0170 | 3 | HG02145.hp1 HG03195.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.337+1418_337+1419d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | |||||
chrX:30678852
|
AT | A | 16 | a0001c0001t0002g0041a0001c0001t0002g0221a0001c0001t0002g0224others(13): Show | 16 | HG00408.hp2 HG01515.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.337+1419delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | |||||
chrX:30678852
|
ATT | A | 6 | a0001c0001t0002g0183a0001c0001t0004g0184a0001c0002t0006g0186others(3): Show | 6 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+1418_337+1419d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30678852 | |||||
chrX:30679220
|
C | CT | 4 | a0001c0001t0001g0086a0001c0002t0006g0186a0001c0002t0006g0187others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1783dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30679220 | |||||
chrX:30679220
|
C | CTT | 1 | a0001c0002t0020g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.337+1782_337+1783d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30679220 | |||||
chrX:30679220
|
CT | C | 3 | a0001c0001t0001g0098a0001c0001t0002g0021a0001c0001t0010g0153 | 3 | HG02735.hp1 HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.337+1783delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30679220 | |||||
chrX:30679293
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.337+1841C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679293 | ||||||
chrX:30679321
|
G | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.337+1869G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679321 | ||||||
chrX:30679379
|
G | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+1927G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679379 | ||||||
chrX:30679446
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0240 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.337+1994G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679446 | ||||||
chrX:30679694
|
G | A | 57 | a0001c0001t0002g0146a0001c0001t0002g0155a0001c0001t0003g0002others(54): Show | 60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.337+2242G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30679694 | ||||||
chrX:30680035
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0002g0248 | 2 | NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.337+2583C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680035 | ||||||
chrX:30680036
|
G | A | 1 | a0001c0001t0018g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.337+2584G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680036 | ||||||
chrX:30680046
|
T | A | 1 | a0001c0001t0002g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.337+2594T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680046 | ||||||
chrX:30680197
|
A | G | 1 | a0001c0002t0020g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.337+2745A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680197 | ||||||
chrX:30680399
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337+2947C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680399 | ||||||
chrX:30680491
|
C | T | 1 | a0001c0001t0009g0115 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.337+3039C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680491 | ||||||
chrX:30680581
|
A | C | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337+3129A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680581 | ||||||
chrX:30680601
|
A | T | 71 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0002g0005others(68): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.337+3149A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680601 | ||||||
chrX:30680761
|
A | T | 2 | a0001c0001t0002g0183a0001c0001t0004g0184 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.337+3309A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680761 | ||||||
chrX:30680866
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.337+3414A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30680866 | ||||||
chrX:30681008
|
T | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337+3556T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681008 | ||||||
chrX:30681050
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.337+3598A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681050 | ||||||
chrX:30681149
|
C | T | 1 | a0001c0001t0004g0182 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.337+3697C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681149 | ||||||
chrX:30681416
|
C | G | 3 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0223 | 3 | HG00099.hp1 HG00323.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.337+3964C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681416 | ||||||
chrX:30681475
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337+4023G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681475 | ||||||
chrX:30681492
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.337+4040A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681492 | ||||||
chrX:30681533
|
C | T | 1 | a0001c0001t0003g0179 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.337+4081C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681533 | ||||||
chrX:30681660
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(220): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.337+4208T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681660 | ||||||
chrX:30681682
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.337+4230G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681682 | ||||||
chrX:30681826
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0002g0021 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.337+4374T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681826 | ||||||
chrX:30681963
|
A | C | 1 | a0001c0001t0005g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.337+4511A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681963 | ||||||
chrX:30681968
|
A | T | 8 | a0001c0001t0004g0016a0001c0001t0004g0172a0001c0001t0004g0174others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+4516A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30681968 | ||||||
chrX:30682127
|
A | AG | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+4680dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30682127 | |||||
chrX:30682360
|
A | G | 1 | a0001c0001t0022g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.337+4908A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682360 | ||||||
chrX:30682732
|
T | C | 1 | a0001c0001t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.337+5280T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682732 | ||||||
chrX:30682944
|
GTA | G | 9 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.337+5493_337+5494d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30682944 | ||||||
chrX:30683192
|
A | G | 1 | a0001c0001t0013g0023 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337+5740A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683192 | ||||||
chrX:30683225
|
T | G | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+5773T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683225 | ||||||
chrX:30683287
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337+5835C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683287 | ||||||
chrX:30683308
|
G | A | 1 | a0001c0001t0002g0248 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.337+5856G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683308 | ||||||
chrX:30683351
|
C | T | 6 | a0001c0001t0002g0214a0001c0001t0002g0236a0001c0001t0002g0242others(3): Show | 6 | HG00741.hp2 HG01070.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+5899C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683351 | ||||||
chrX:30683531
|
TTGG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6083_337+6085d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30683531 | |||||
chrX:30683538
|
C | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6086C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683538 | ||||||
chrX:30683542
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6090G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683542 | ||||||
chrX:30683543
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6091G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683543 | ||||||
chrX:30683544
|
C | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6092C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683544 | ||||||
chrX:30683546
|
T | TCGCG | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6094_337+6095i others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683546 | ||||||
chrX:30683547
|
A | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6095A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683547 | ||||||
chrX:30683549
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6097G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683549 | ||||||
chrX:30683550
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6098C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683550 | ||||||
chrX:30683886
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6434G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683886 | ||||||
chrX:30683887
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6435G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30683887 | ||||||
chrX:30683888
|
CCTTGGGC others(4): Show |
C | 1 | a0001c0001t0001g0062 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.337+6441_337+6451d others(13): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30683888 | |||||
chrX:30684000
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.337+6553delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684000 | |||||
chrX:30684063
|
T | TCTAA | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(200): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.337+6614_337+6615i others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684063 | |||||
chrX:30684216
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0078others(5): Show | 8 | HG00323.hp1 HG01175.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+6764C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684216 | ||||||
chrX:30684359
|
A | AT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-6761dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684359 | |||||
chrX:30684367
|
T | TA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-6751dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684367 | |||||
chrX:30684423
|
T | TG | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.338-6697dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684423 | |||||
chrX:30684423
|
TG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-6697delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684423 | |||||
chrX:30684432
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.338-6691C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684432 | ||||||
chrX:30684436
|
T | TG | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-6684dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684436 | |||||
chrX:30684527
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.338-6596G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684527 | ||||||
chrX:30684580
|
C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | NA18956.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-6543C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684580 | ||||||
chrX:30684666
|
C | CA | 24 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0006others(21): Show | 27 | HG00408.hp1 HG01074.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.338-6429dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
C | CAA | 4 | a0001c0001t0003g0011a0001c0001t0003g0013a0001c0001t0003g0137others(1): Show | 4 | HG02080.hp2 HG02280.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-6430_338-6429d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
C | CAAAA | 1 | a0001c0002t0006g0187 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.338-6432_338-6429d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
C | CAAAAA | 2 | a0001c0002t0006g0186a0001c0002t0006g0188 | 2 | HG01099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.338-6433_338-6429d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
C | CAAAAAA | 1 | a0001c0002t0020g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.338-6434_338-6429d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CA | C | 3 | a0001c0001t0004g0171a0001c0001t0011g0181a0001c0001t0014g0185 | 3 | HG02965.hp1 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.338-6429delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAA | C | 1 | a0001c0003t0003g0170 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.338-6430_338-6429d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAAA | C | 1 | a0001c0001t0002g0093 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.338-6431_338-6429d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAAAA | C | 33 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0051others(30): Show | 33 | HG00544.hp2 HG01175.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.338-6432_338-6429d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAAAAA | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(154): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.338-6433_338-6429d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAAAAAA | C | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.338-6434_338-6429d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684666
|
CAAAAAAA | C | 1 | a0001c0001t0003g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.338-6435_338-6429d others(9): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684666 | |||||
chrX:30684813
|
T | TA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-6307dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30684813 | |||||
chrX:30684926
|
T | C | 11 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 11 | HG01515.hp1 HG01517.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-6197T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684926 | ||||||
chrX:30684966
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.338-6157C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30684966 | ||||||
chrX:30685128
|
C | CT | 2 | a0001c0001t0002g0264a0001c0001t0008g0165 | 2 | HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.338-5984dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685128 | |||||
chrX:30685128
|
CT | C | 2 | a0001c0001t0002g0231a0001c0001t0002g0262 | 2 | HG01496.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.338-5984delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685128 | |||||
chrX:30685134
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.338-5989T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685134 | ||||||
chrX:30685289
|
TC | T | 1 | a0001c0001t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-5831delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685289 | |||||
chrX:30685296
|
TA | T | 1 | a0001c0001t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-5825delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685296 | |||||
chrX:30685366
|
C | G | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.338-5757C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685366 | ||||||
chrX:30685389
|
TC | T | 1 | a0001c0001t0001g0077 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.338-5731delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685389 | |||||
chrX:30685439
|
A | AT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-5676dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685439 | |||||
chrX:30685519
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.338-5604C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685519 | ||||||
chrX:30685735
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-5387dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685735 | |||||
chrX:30685769
|
G | T | 1 | a0001c0001t0003g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.338-5354G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30685769 | ||||||
chrX:30685789
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-5330dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30685789 | |||||
chrX:30686030
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(195): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.338-5093T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686030 | ||||||
chrX:30686125
|
T | C | 1 | a0001c0003t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338-4998T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686125 | ||||||
chrX:30686168
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-4952delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30686168 | |||||
chrX:30686221
|
G | GA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-4901dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30686221 | |||||
chrX:30686367
|
A | G | 1 | a0001c0001t0003g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.338-4756A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686367 | ||||||
chrX:30686388
|
A | G | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-4735A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686388 | ||||||
chrX:30686396
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-4725dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30686396 | |||||
chrX:30686451
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.338-4672T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686451 | ||||||
chrX:30686606
|
G | GT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-4513dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30686606 | |||||
chrX:30686716
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.338-4407T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686716 | ||||||
chrX:30686797
|
A | C | 2 | a0001c0001t0007g0102a0001c0001t0007g0103 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.338-4326A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686797 | ||||||
chrX:30686969
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-4154C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30686969 | ||||||
chrX:30687165
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(86): Show | 92 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.338-3958C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687165 | ||||||
chrX:30687518
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-3603dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30687518 | |||||
chrX:30687696
|
T | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-3427T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687696 | ||||||
chrX:30687978
|
C | T | 2 | a0001c0003t0003g0167a0001c0003t0003g0170 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.338-3145C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30687978 | ||||||
chrX:30688306
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.338-2817C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688306 | ||||||
chrX:30688307
|
TG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2813delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688307 | |||||
chrX:30688383
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2736delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688383 | |||||
chrX:30688397
|
G | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 64 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.338-2726G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688397 | ||||||
chrX:30688423
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2697delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688423 | |||||
chrX:30688501
|
C | CA | 16 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0076others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-2601dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688501 | |||||
chrX:30688501
|
C | CAA | 1 | a0001c0001t0001g0070 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.338-2602_338-2601d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688501 | |||||
chrX:30688501
|
CA | C | 16 | a0001c0001t0001g0195a0001c0001t0002g0214a0001c0001t0003g0113others(13): Show | 16 | HG00099.hp2 HG01496.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-2601delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688501 | |||||
chrX:30688586
|
CT | C | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2533delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688586 | |||||
chrX:30688617
|
AG | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2504delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688617 | |||||
chrX:30688658
|
G | GC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2463dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688658 | |||||
chrX:30688664
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2455delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688664 | |||||
chrX:30688744
|
T | TG | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2375dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688744 | |||||
chrX:30688757
|
T | TA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2362dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688757 | |||||
chrX:30688772
|
TG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2348delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688772 | |||||
chrX:30688863
|
G | GA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2254dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30688863 | |||||
chrX:30688911
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.338-2212G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688911 | ||||||
chrX:30688926
|
A | G | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-2197A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688926 | ||||||
chrX:30688929
|
G | A | 7 | a0001c0001t0004g0172a0001c0001t0004g0174a0001c0001t0004g0175others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.338-2194G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688929 | ||||||
chrX:30688932
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.338-2191T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688932 | ||||||
chrX:30688956
|
T | C | 1 | a0001c0003t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338-2167T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30688956 | ||||||
chrX:30689077
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2041delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30689077 | |||||
chrX:30689099
|
AC | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-2023delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689099 | ||||||
chrX:30689158
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.338-1965G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689158 | ||||||
chrX:30689326
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-1795dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30689326 | |||||
chrX:30689330
|
T | A | 1 | a0001c0001t0003g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.338-1793T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689330 | ||||||
chrX:30689337
|
G | A | 1 | a0001c0001t0012g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.338-1786G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689337 | ||||||
chrX:30689487
|
A | AG | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-1636_338-1635i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689487 | ||||||
chrX:30689585
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-1535delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30689585 | |||||
chrX:30689767
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(218): Show | 225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.338-1356G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689767 | ||||||
chrX:30689837
|
C | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-1286C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689837 | ||||||
chrX:30689870
|
GC | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-1251delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30689870 | |||||
chrX:30689888
|
C | G | 2 | a0001c0002t0006g0186a0001c0002t0006g0188 | 2 | HG01099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.338-1235C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30689888 | ||||||
chrX:30689957
|
A | AC | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.338-1163dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30689957 | |||||
chrX:30690035
|
A | G | 1 | a0001c0001t0005g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.338-1088A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690035 | ||||||
chrX:30690222
|
T | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-901T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690222 | ||||||
chrX:30690223
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-900G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690223 | ||||||
chrX:30690226
|
A | C | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-897A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690226 | ||||||
chrX:30690313
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.338-810G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690313 | ||||||
chrX:30690438
|
G | GT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-682dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30690438 | |||||
chrX:30690447
|
AG | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-671delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30690447 | |||||
chrX:30690537
|
GA | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-583delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30690537 | |||||
chrX:30690631
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.338-492G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690631 | ||||||
chrX:30690826
|
A | G | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.338-297A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | chrX | 30690826 | ||||||
chrX:30690945
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-173delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30690945 | |||||
chrX:30690971
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-149delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30690971 | |||||
chrX:30691080
|
TA | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.338-40delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 30691080 | |||||
chrX:30691323
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+127delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691323 | |||||
chrX:30691327
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.414+128G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691327 | ||||||
chrX:30691358
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+162delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691358 | |||||
chrX:30691432
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.414+233C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691432 | ||||||
chrX:30691434
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+238delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691434 | |||||
chrX:30691468
|
C | CT | 14 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0052others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+290dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691468 | |||||
chrX:30691468
|
C | CTT | 1 | a0001c0001t0019g0112 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.414+289_414+290dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691468 | |||||
chrX:30691468
|
CT | C | 33 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0080others(30): Show | 33 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.414+290delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691468 | |||||
chrX:30691600
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+401G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691600 | ||||||
chrX:30691643
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG02109.hp1 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.414+444T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691643 | ||||||
chrX:30691662
|
TG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+467delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691662 | |||||
chrX:30691703
|
A | AC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+506dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691703 | |||||
chrX:30691834
|
GT | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+640delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691834 | |||||
chrX:30691888
|
TATTGA | T | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+691_414+695del others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691888 | |||||
chrX:30691902
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+705delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30691902 | |||||
chrX:30691961
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.414+762A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30691961 | ||||||
chrX:30692012
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+821delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692012 | |||||
chrX:30692068
|
TTTTCTGT others(19): Show |
T | 73 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0002g0005others(70): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.414+872_414+897del others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692068 | |||||
chrX:30692196
|
T | TC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1003dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692196 | |||||
chrX:30692313
|
G | GC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1115dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692313 | |||||
chrX:30692342
|
C | CT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1147dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692342 | |||||
chrX:30692356
|
AC | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1162delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692356 | |||||
chrX:30692425
|
CT | C | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1230delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692425 | |||||
chrX:30692437
|
C | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.414+1238C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692437 | ||||||
chrX:30692485
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1296delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692485 | |||||
chrX:30692502
|
A | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1303A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692502 | ||||||
chrX:30692713
|
G | GC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1516dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692713 | |||||
chrX:30692724
|
TG | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1526delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692724 | ||||||
chrX:30692728
|
G | GGGAGA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1531_414+1532i others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692728 | |||||
chrX:30692731
|
T | G | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1532T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30692731 | ||||||
chrX:30692747
|
AC | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1550delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692747 | |||||
chrX:30692784
|
A | AT | 8 | a0001c0001t0004g0016a0001c0001t0004g0172a0001c0001t0004g0174others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+1597dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692784 | |||||
chrX:30692784
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414+1597delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692784 | |||||
chrX:30692966
|
A | AATC | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1431_415-1429d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30692966 | |||||
chrX:30693000
|
C | CT | 1 | a0001c0001t0002g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.415-1395dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693000 | |||||
chrX:30693006
|
CTTTTCTT others(5): Show |
C | 2 | a0001c0001t0002g0237a0001c0001t0002g0241 | 2 | HG00597.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.415-1389_415-1378d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693006 | |||||
chrX:30693011
|
C | CT | 28 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0067others(25): Show | 28 | HG00597.hp1 HG00621.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.415-1366dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | |||||
chrX:30693011
|
C | CTT | 3 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188 | 3 | HG01099.hp1 HG01168.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.415-1367_415-1366d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | |||||
chrX:30693011
|
C | CTTT | 1 | a0001c0002t0020g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.415-1368_415-1366d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | |||||
chrX:30693011
|
CT | C | 14 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(11): Show | 14 | HG00099.hp1 HG00323.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-1366delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693011 | |||||
chrX:30693016
|
T | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0030others(1): Show | 4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1384T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30693016 | ||||||
chrX:30693272
|
TC | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-1125delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693272 | |||||
chrX:30693287
|
A | AT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-1111dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693287 | |||||
chrX:30693363
|
G | GT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-1034dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693363 | |||||
chrX:30693387
|
G | GT | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-1011dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693387 | |||||
chrX:30693406
|
CA | C | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-992delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693406 | |||||
chrX:30693452
|
T | TC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-947dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693452 | |||||
chrX:30693470
|
T | TC | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-927dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693470 | |||||
chrX:30693558
|
AT | A | 1 | a0001c0001t0002g0240 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.415-834delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30693558 | |||||
chrX:30693688
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(143): Show | 149 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.415-712G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30693688 | ||||||
chrX:30694151
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0002g0021 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.415-249G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | chrX | 30694151 | ||||||
chrX:30694351
|
T | TA | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.415-46dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | 30694351 | |||||
chrX:30694578
|
A | G | 2 | a0001c0001t0003g0160a0001c0001t0003g0166 | 2 | HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.552+41A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694578 | ||||||
chrX:30694679
|
G | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(216): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.552+142G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694679 | ||||||
chrX:30694724
|
AT | A | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.552+193delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 30694724 | |||||
chrX:30694732
|
T | G | 3 | a0001c0001t0004g0174a0001c0001t0023g0173a0001c0004t0017g0111 | 3 | HG01884.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.552+195T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30694732 | ||||||
chrX:30695318
|
G | T | 1 | a0001c0001t0003g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.553-724G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695318 | ||||||
chrX:30695592
|
A | C | 1 | a0001c0001t0003g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.553-450A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695592 | ||||||
chrX:30695798
|
G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-244G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695798 | ||||||
chrX:30695846
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(87): Show | 93 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.553-196A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695846 | ||||||
chrX:30695940
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-102C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 6/20 | chrX | 30695940 | ||||||
chrX:30696336
|
C | CA | 18 | a0001c0001t0002g0183a0001c0001t0002g0236a0001c0001t0002g0245others(15): Show | 18 | HG00741.hp2 HG01070.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.662+188dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 30696336 | |||||
chrX:30696399
|
T | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-218T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | chrX | 30696399 | ||||||
chrX:30696443
|
A | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-174A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 7/20 | chrX | 30696443 | ||||||
chrX:30696700
|
C | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+17C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696700 | ||||||
chrX:30696723
|
C | A | 2 | a0001c0001t0001g0032a0001c0001t0002g0244 | 2 | HG01258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.729+40C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696723 | ||||||
chrX:30696735
|
C | CA | 1 | a0001c0001t0001g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.729+61dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 30696735 | |||||
chrX:30696735
|
CA | C | 1 | a0001c0001t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.729+61delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 30696735 | |||||
chrX:30696744
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729+61A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696744 | ||||||
chrX:30696963
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.729+280T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30696963 | ||||||
chrX:30697008
|
G | A | 8 | a0001c0001t0004g0016a0001c0001t0004g0172a0001c0001t0004g0174others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+325G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697008 | ||||||
chrX:30697334
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.730-398G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697334 | ||||||
chrX:30697385
|
T | G | 4 | a0001c0001t0007g0102a0001c0001t0007g0103a0001c0001t0008g0101others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-347T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697385 | ||||||
chrX:30697480
|
T | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-252T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697480 | ||||||
chrX:30697710
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(199): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.730-22C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 8/20 | chrX | 30697710 | ||||||
chrX:30697923
|
T | C | 3 | a0001c0001t0003g0114a0001c0001t0003g0143a0001c0001t0009g0144 | 3 | HG00558.hp1 HG02071.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.747+174T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30697923 | ||||||
chrX:30697968
|
G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+219G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30697968 | ||||||
chrX:30698004
|
A | G | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.747+255A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698004 | ||||||
chrX:30698319
|
T | G | 1 | a0001c0001t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747+570T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698319 | ||||||
chrX:30698464
|
G | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+715G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698464 | ||||||
chrX:30698599
|
G | T | 75 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0002g0005others(72): Show | 76 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.747+850G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698599 | ||||||
chrX:30698680
|
G | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.747+931G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698680 | ||||||
chrX:30698683
|
G | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+934G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698683 | ||||||
chrX:30698701
|
C | CA | 9 | a0001c0001t0002g0238a0001c0001t0003g0206a0001c0001t0004g0171others(6): Show | 9 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+967dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | |||||
chrX:30698701
|
C | CAA | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.747+966_747+967dup others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | |||||
chrX:30698701
|
C | CAAA | 10 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0079others(7): Show | 10 | HG00597.hp2 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.747+965_747+967dup others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | |||||
chrX:30698701
|
C | CAAAA | 1 | a0001c0002t0006g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.747+964_747+967dup others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698701 | |||||
chrX:30698823
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0108 | 2 | HG00423.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.747+1074G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698823 | ||||||
chrX:30698866
|
C | CA | 2 | a0001c0001t0002g0216a0001c0001t0002g0270 | 2 | HG00323.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.747+1135dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | |||||
chrX:30698866
|
C | CAA | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(179): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.747+1134_747+1135d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | |||||
chrX:30698866
|
C | CAAA | 14 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0002g0091others(11): Show | 14 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+1133_747+1135d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | |||||
chrX:30698866
|
CA | C | 1 | a0001c0001t0003g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.747+1135delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698866 | |||||
chrX:30698880
|
A | AAG | 1 | a0001c0001t0001g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.747+1132_747+1133i others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30698880 | |||||
chrX:30698881
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009 | 3 | HG01515.hp1 HG01517.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.747+1132A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698881 | ||||||
chrX:30698885
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747+1136G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30698885 | ||||||
chrX:30699161
|
C | G | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.748-1253C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699161 | ||||||
chrX:30699175
|
T | TTA | 3 | a0001c0001t0001g0213a0001c0001t0002g0248a0001c0001t0002g0256 | 3 | NA18942.hp2 NA18999.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.748-1225_748-1224d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699175 | |||||
chrX:30699214
|
T | TACATGTT others(20): Show |
15 | a0001c0001t0001g0265a0001c0001t0002g0207a0001c0001t0002g0208others(12): Show | 15 | HG01361.hp1 HG01891.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.748-1166_748-1140d others(29): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699214 | |||||
chrX:30699214
|
TACATGTT others(20): Show |
T | 6 | a0001c0001t0003g0006a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-1166_748-1140d others(29): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699214 | |||||
chrX:30699220
|
T | TTA | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748-1187_748-1186d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699220 | |||||
chrX:30699249
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0192 | 2 | HG03704.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.748-1165A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699249 | ||||||
chrX:30699267
|
TAACATGT others(8): Show |
T | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748-1139_748-1125d others(17): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699267 | |||||
chrX:30699273
|
G | GTTATATA others(18): Show |
1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.748-1140_748-1139i others(27): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699273 | |||||
chrX:30699273
|
GTA | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.748-1134_748-1133d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699273 | |||||
chrX:30699275
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.748-1139A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699275 | ||||||
chrX:30699280
|
TAC | T | 1 | a0001c0001t0002g0227 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.748-1132_748-1131d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699280 | |||||
chrX:30699298
|
A | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0009 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.748-1116A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699298 | ||||||
chrX:30699317
|
G | GTT | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(191): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.748-1096_748-1095d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699317 | |||||
chrX:30699318
|
T | TTA | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.748-1083_748-1082d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699318 | |||||
chrX:30699320
|
A | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(87): Show | 93 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.748-1094A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699320 | ||||||
chrX:30699331
|
T | C | 5 | a0001c0001t0003g0126a0001c0001t0003g0134a0001c0001t0003g0137others(2): Show | 5 | HG00621.hp1 HG02897.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-1083T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699331 | ||||||
chrX:30699368
|
C | CT | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.748-1031dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699368 | |||||
chrX:30699368
|
C | CTT | 3 | a0001c0001t0002g0257a0001c0001t0002g0258a0001c0001t0016g0272 | 3 | HG01070.hp2 HG01071.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.748-1032_748-1031d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699368 | |||||
chrX:30699368
|
CT | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-1031delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30699368 | |||||
chrX:30699552
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.748-862T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699552 | ||||||
chrX:30699555
|
G | T | 5 | a0001c0001t0002g0251a0001c0002t0006g0186a0001c0002t0006g0187others(2): Show | 5 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-859G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699555 | ||||||
chrX:30699595
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-819C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699595 | ||||||
chrX:30699630
|
C | T | 1 | a0001c0001t0011g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.748-784C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699630 | ||||||
chrX:30699660
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.748-754G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699660 | ||||||
chrX:30699931
|
T | C | 2 | a0001c0001t0002g0210a0001c0001t0002g0259 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.748-483T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30699931 | ||||||
chrX:30700126
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.748-288C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700126 | ||||||
chrX:30700145
|
T | TACTA | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.748-258_748-255dup others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | 30700145 | |||||
chrX:30700248
|
A | G | 2 | a0001c0001t0003g0120a0001c0001t0003g0123 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.748-166A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700248 | ||||||
chrX:30700367
|
G | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.748-47G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700367 | ||||||
chrX:30700409
|
A | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0245 | 2 | HG00741.hp2 HG01070.hp1 |
splice_region_variant&intron_variant | LOW | c.748-5A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 9/20 | chrX | 30700409 | ||||||
chrX:30700759
|
A | AAAAT | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(204): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.784-78_784-75dupAA others(2): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | 30700759 | |||||
chrX:30700953
|
T | C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.851+48T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30700953 | ||||||
chrX:30701239
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(198): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.851+334A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701239 | ||||||
chrX:30701375
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(202): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.851+470T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701375 | ||||||
chrX:30701376
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851+471G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701376 | ||||||
chrX:30701463
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+558T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701463 | ||||||
chrX:30701606
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.851+701T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701606 | ||||||
chrX:30701639
|
G | T | 1 | a0001c0003t0003g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.851+734G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701639 | ||||||
chrX:30701653
|
C | G | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.851+748C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30701653 | ||||||
chrX:30701985
|
CTA | C | 1 | a0001c0001t0002g0097 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.851+1084_851+1085d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30701985 | |||||
chrX:30702047
|
A | AT | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0065others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+1154dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30702047 | |||||
chrX:30702047
|
AT | A | 1 | a0001c0001t0001g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.851+1154delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30702047 | |||||
chrX:30702051
|
T | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1146T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702051 | ||||||
chrX:30702075
|
T | TC | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+1171dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30702075 | |||||
chrX:30702078
|
T | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+1173T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702078 | ||||||
chrX:30702191
|
C | T | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+1286C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702191 | ||||||
chrX:30702233
|
A | G | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+1328A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702233 | ||||||
chrX:30702261
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.851+1356C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702261 | ||||||
chrX:30702288
|
C | T | 7 | a0001c0001t0004g0172a0001c0001t0004g0174a0001c0001t0004g0175others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+1383C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702288 | ||||||
chrX:30702322
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0109 | 3 | HG02647.hp1 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.851+1417G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702322 | ||||||
chrX:30702378
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.851+1473A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702378 | ||||||
chrX:30702433
|
A | G | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1528A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702433 | ||||||
chrX:30702641
|
T | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1736T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702641 | ||||||
chrX:30702685
|
A | G | 1 | a0001c0001t0011g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.851+1780A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702685 | ||||||
chrX:30702707
|
T | C | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.851+1802T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702707 | ||||||
chrX:30702951
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851+2046A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702951 | ||||||
chrX:30702981
|
C | T | 7 | a0001c0001t0005g0100a0001c0001t0005g0104a0001c0001t0005g0203others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+2076C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30702981 | ||||||
chrX:30703012
|
C | A | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.851+2107C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703012 | ||||||
chrX:30703097
|
T | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+2192T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703097 | ||||||
chrX:30703417
|
C | G | 1 | a0001c0001t0005g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.851+2512C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703417 | ||||||
chrX:30703511
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(180): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.851+2606G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703511 | ||||||
chrX:30703777
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851+2872A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703777 | ||||||
chrX:30703781
|
C | G | 4 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0223others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+2876C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30703781 | ||||||
chrX:30703956
|
C | CA | 6 | a0001c0001t0002g0212a0001c0001t0003g0116a0001c0001t0003g0161others(3): Show | 6 | HG02451.hp1 HG02965.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+3063dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30703956 | |||||
chrX:30703956
|
CA | C | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.851+3063delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30703956 | |||||
chrX:30704128
|
T | TATATATA others(24): Show |
2 | a0001c0001t0005g0105a0001c0001t0007g0102 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.851+3223_851+3224i others(33): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704128 | ||||||
chrX:30704128
|
T | TTA | 73 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0002g0005others(70): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.851+3243_851+3244d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATA | 3 | a0001c0001t0002g0212a0001c0001t0002g0236a0001c0001t0002g0245 | 3 | HG00741.hp2 HG01070.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.851+3241_851+3244d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATA | 3 | a0001c0001t0002g0237a0001c0001t0012g0110a0001c0001t0012g0164 | 3 | HG00597.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.851+3239_851+3244d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(1): Show |
2 | a0001c0001t0005g0104a0001c0002t0006g0186 | 2 | HG01099.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.851+3237_851+3244d others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(3): Show |
1 | a0001c0002t0006g0187 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.851+3235_851+3244d others(12): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(5): Show |
2 | a0001c0002t0006g0188a0001c0002t0020g0189 | 2 | HG00741.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.851+3233_851+3244d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(7): Show |
56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(53): Show | 59 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.851+3231_851+3244d others(16): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(9): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0052a0001c0001t0001g0059others(11): Show | 14 | HG00597.hp1 HG01255.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.851+3229_851+3244d others(18): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(11): Show |
9 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0048others(6): Show | 9 | HG02572.hp1 HG02683.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+3227_851+3244d others(20): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(13): Show |
7 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0044others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+3225_851+3244d others(22): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0002g0168 | 3 | HG01884.hp2 HG03834.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(24): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(26): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(19): Show |
3 | a0001c0001t0001g0018a0001c0001t0004g0177a0001c0001t0014g0185 | 3 | HG02615.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(28): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(21): Show |
2 | a0001c0001t0005g0203a0001c0001t0023g0173 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(30): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(23): Show |
7 | a0001c0001t0001g0032a0001c0001t0002g0092a0001c0001t0004g0171others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(32): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(25): Show |
3 | a0001c0001t0002g0091a0001c0001t0004g0175a0001c0001t0004g0176 | 3 | HG02055.hp1 HG02293.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.851+3244_851+3245i others(34): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(27): Show |
6 | a0001c0001t0002g0093a0001c0001t0002g0095a0001c0001t0002g0096others(3): Show | 6 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(36): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(29): Show |
4 | a0001c0001t0004g0174a0001c0001t0005g0100a0001c0001t0008g0165others(1): Show | 4 | HG02809.hp2 HG02897.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+3244_851+3245i others(38): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(31): Show |
1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(40): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0002g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(42): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
TTA | T | 1 | a0001c0001t0011g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851+3243_851+3244d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704128
|
TTATATA | T | 1 | a0001c0001t0015g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.851+3239_851+3244d others(8): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704128 | |||||
chrX:30704149
|
T | TATATATA others(37): Show |
1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.851+3244_851+3245i others(46): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704149 | ||||||
chrX:30704243
|
C | G | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.852-3313C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704243 | ||||||
chrX:30704417
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.852-3139C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704417 | ||||||
chrX:30704495
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-3061C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704495 | ||||||
chrX:30704576
|
A | G | 1 | a0001c0001t0004g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.852-2980A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704576 | ||||||
chrX:30704577
|
C | CT | 19 | a0001c0001t0002g0093a0001c0001t0002g0236a0001c0001t0002g0245others(16): Show | 19 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.852-2966dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704577 | |||||
chrX:30704604
|
G | A | 1 | a0001c0001t0003g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.852-2952G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704604 | ||||||
chrX:30704611
|
C | CG | 1 | a0001c0001t0003g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.852-2945_852-2944i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704611 | ||||||
chrX:30704612
|
A | C | 1 | a0001c0001t0003g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.852-2944A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704612 | ||||||
chrX:30704696
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(187): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.852-2860C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704696 | ||||||
chrX:30704855
|
C | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(85): Show | 91 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.852-2701C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704855 | ||||||
chrX:30704859
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(187): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.852-2697C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704859 | ||||||
chrX:30704870
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(201): Show | 208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.852-2686G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30704870 | ||||||
chrX:30704893
|
G | GT | 1 | a0001c0001t0003g0137 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.852-2661dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30704893 | |||||
chrX:30705096
|
A | C | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.852-2460A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705096 | ||||||
chrX:30705262
|
A | G | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.852-2294A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705262 | ||||||
chrX:30705345
|
A | G | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.852-2211A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705345 | ||||||
chrX:30705374
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-2182C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705374 | ||||||
chrX:30705851
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.852-1705A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705851 | ||||||
chrX:30705876
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(200): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.852-1680C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705876 | ||||||
chrX:30705910
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.852-1646C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30705910 | ||||||
chrX:30706055
|
G | A | 8 | a0001c0001t0005g0100a0001c0001t0005g0104a0001c0001t0005g0203others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.852-1501G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706055 | ||||||
chrX:30706057
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.852-1499C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706057 | ||||||
chrX:30706065
|
C | T | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.852-1491C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706065 | ||||||
chrX:30706209
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(194): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.852-1347G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706209 | ||||||
chrX:30706272
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.852-1284G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706272 | ||||||
chrX:30706286
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.852-1270C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706286 | ||||||
chrX:30706434
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852-1122C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706434 | ||||||
chrX:30706476
|
CG | C | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.852-1076delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30706476 | |||||
chrX:30706500
|
C | G | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.852-1056C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706500 | ||||||
chrX:30706546
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.852-1010A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706546 | ||||||
chrX:30706699
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.852-857G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706699 | ||||||
chrX:30706767
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048 | 3 | HG02572.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852-789C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706767 | ||||||
chrX:30706850
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.852-706C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706850 | ||||||
chrX:30706898
|
A | T | 1 | a0001c0001t0003g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.852-658A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706898 | ||||||
chrX:30706985
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.852-571C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30706985 | ||||||
chrX:30707105
|
T | C | 1 | a0001c0001t0011g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.852-451T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30707105 | ||||||
chrX:30707307
|
T | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-249T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | chrX | 30707307 | ||||||
chrX:30707328
|
C | CA | 18 | a0001c0001t0001g0057a0001c0001t0003g0004a0001c0001t0003g0122others(15): Show | 19 | HG00408.hp1 HG00609.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.852-211dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30707328 | |||||
chrX:30707328
|
CA | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0075a0001c0001t0003g0133 | 3 | HG01993.hp1 HG02523.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.852-211delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30707328 | |||||
chrX:30707449
|
CT | C | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.852-101delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 30707449 | |||||
chrX:30707614
|
TA | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.894+22delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 30707614 | |||||
chrX:30707677
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(181): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.894+79C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707677 | ||||||
chrX:30707731
|
CAATACAA | C | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.894+137_894+143del others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 30707731 | |||||
chrX:30707755
|
A | G | 2 | a0001c0001t0007g0102a0001c0001t0007g0103 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.894+157A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707755 | ||||||
chrX:30707806
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(201): Show | 208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.894+208C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707806 | ||||||
chrX:30707936
|
A | T | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-118A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707936 | ||||||
chrX:30707986
|
TA | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.895-60delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 30707986 | |||||
chrX:30707997
|
T | A | 1 | a0001c0001t0002g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.895-57T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | chrX | 30707997 | ||||||
chrX:30708032
|
C | CT | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.895-12dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 30708032 | |||||
chrX:30708032
|
CT | C | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.895-12delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | 30708032 | |||||
chrX:30708400
|
G | GT | 2 | a0001c0001t0001g0075a0001c0001t0001g0086 | 2 | HG01978.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.975+280dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30708400 | |||||
chrX:30708400
|
GT | G | 13 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(10): Show | 13 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.975+280delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30708400 | |||||
chrX:30708715
|
A | G | 2 | a0001c0001t0002g0217a0001c0001t0016g0272 | 2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.975+581A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30708715 | ||||||
chrX:30708735
|
AG | A | 1 | a0001c0001t0002g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.975+602delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30708735 | ||||||
chrX:30708988
|
C | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(196): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.975+854C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30708988 | ||||||
chrX:30709171
|
G | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.975+1037G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709171 | ||||||
chrX:30709216
|
CT | C | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+1089delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30709216 | |||||
chrX:30709233
|
TG | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+1102delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30709233 | |||||
chrX:30709258
|
A | G | 1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.975+1124A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709258 | ||||||
chrX:30709304
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.975+1170G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709304 | ||||||
chrX:30709385
|
AC | A | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+1254delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30709385 | |||||
chrX:30709401
|
TA | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+1269delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30709401 | |||||
chrX:30709426
|
G | A | 4 | a0001c0001t0002g0235a0001c0001t0002g0252a0001c0001t0002g0254others(1): Show | 4 | HG01928.hp1 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+1292G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709426 | ||||||
chrX:30709708
|
CTAA | C | 1 | a0001c0001t0001g0017 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.975+1577_975+1579d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30709708 | |||||
chrX:30709972
|
TC | T | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.975+1839delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30709972 | ||||||
chrX:30710385
|
G | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.975+2251G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710385 | ||||||
chrX:30710461
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(192): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.975+2327T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710461 | ||||||
chrX:30710861
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0124a0001c0001t0003g0151 | 4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+2727T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30710861 | ||||||
chrX:30710968
|
TC | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+2839delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30710968 | |||||
chrX:30711053
|
G | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(192): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.975+2919G>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711053 | ||||||
chrX:30711113
|
CT | C | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+2986delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30711113 | |||||
chrX:30711116
|
T | C | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975+2982T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711116 | ||||||
chrX:30711127
|
C | CT | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.975+3004dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30711127 | |||||
chrX:30711127
|
C | CTT | 2 | a0001c0001t0002g0089a0001c0001t0002g0242 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+3003_975+3004d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30711127 | |||||
chrX:30711138
|
T | TTC | 1 | a0001c0001t0002g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.975+3004_975+3005i others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711138 | ||||||
chrX:30711225
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(193): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.975+3091A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711225 | ||||||
chrX:30711238
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.975+3104G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711238 | ||||||
chrX:30711292
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.975+3158G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30711292 | ||||||
chrX:30711574
|
AC | A | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+3443delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30711574 | |||||
chrX:30712414
|
TG | T | 2 | a0001c0001t0001g0075a0001c0001t0003g0161 | 2 | NA19054.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.975+4285delG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712414 | |||||
chrX:30712556
|
CT | C | 5 | a0001c0001t0002g0210a0001c0001t0002g0259a0001c0001t0002g0263others(2): Show | 5 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+4432delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712556 | |||||
chrX:30712589
|
GT | G | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+4460delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712589 | |||||
chrX:30712625
|
G | A | 4 | a0001c0001t0002g0216a0001c0001t0002g0218a0001c0001t0002g0223others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4491G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30712625 | ||||||
chrX:30712711
|
TC | T | 1 | a0001c0001t0002g0225 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.975+4578delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30712711 | ||||||
chrX:30712717
|
C | CT | 23 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0086others(20): Show | 23 | HG00597.hp1 HG00597.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.975+4608dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712717
|
C | CTT | 1 | a0001c0001t0021g0222 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.975+4607_975+4608d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712717
|
CT | C | 24 | a0001c0001t0001g0063a0001c0001t0001g0190a0001c0001t0001g0193others(21): Show | 24 | HG01515.hp1 HG01517.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.975+4608delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712717
|
CTTTT | C | 2 | a0001c0001t0005g0100a0001c0001t0007g0102 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.975+4605_975+4608d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712717
|
CTTTTT | C | 8 | a0001c0001t0005g0022a0001c0001t0005g0104a0001c0001t0005g0105others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+4604_975+4608d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712717
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4597_975+4608d others(14): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30712717 | |||||
chrX:30712964
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.975+4830G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30712964 | ||||||
chrX:30713063
|
C | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+4929C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713063 | ||||||
chrX:30713074
|
G | GA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+4942dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713074 | |||||
chrX:30713085
|
TC | T | 1 | a0001c0001t0001g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.975+4953delC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713085 | |||||
chrX:30713142
|
GT | G | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+5013delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713142 | |||||
chrX:30713185
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(191): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.975+5051T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713185 | ||||||
chrX:30713206
|
C | A | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+5072C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713206 | ||||||
chrX:30713249
|
T | TC | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.975+5116dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713249 | |||||
chrX:30713402
|
T | C | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.976-5136T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30713402 | ||||||
chrX:30713709
|
G | GA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-4825dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713709 | |||||
chrX:30713822
|
C | CA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-4711dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713822 | |||||
chrX:30713906
|
CTAGAA | C | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-4629_976-4625d others(7): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30713906 | |||||
chrX:30714141
|
G | A | 3 | a0001c0001t0003g0004a0001c0001t0003g0124a0001c0001t0003g0151 | 4 | HG00408.hp1 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-4397G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714141 | ||||||
chrX:30714219
|
A | G | 2 | a0001c0003t0003g0167a0001c0003t0003g0170 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.976-4319A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714219 | ||||||
chrX:30714542
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.976-3996C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714542 | ||||||
chrX:30714551
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(199): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.976-3987T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714551 | ||||||
chrX:30714619
|
T | C | 4 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0030others(1): Show | 4 | HG02970.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-3919T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714619 | ||||||
chrX:30714759
|
G | GT | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3779_976-3778i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714759 | ||||||
chrX:30714798
|
A | AC | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3739dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30714798 | |||||
chrX:30714828
|
T | A | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3710T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714828 | ||||||
chrX:30714832
|
G | A | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-3706G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714832 | ||||||
chrX:30714859
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.976-3679G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714859 | ||||||
chrX:30714926
|
T | C | 1 | a0001c0001t0003g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.976-3612T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30714926 | ||||||
chrX:30715044
|
A | AT | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3493dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30715044 | |||||
chrX:30715066
|
C | CA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3468dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30715066 | |||||
chrX:30715106
|
A | AT | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3429dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30715106 | |||||
chrX:30715261
|
G | GA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3272dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30715261 | |||||
chrX:30715326
|
C | A | 1 | a0001c0001t0002g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.976-3212C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715326 | ||||||
chrX:30715330
|
A | AG | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-3207dupG | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30715330 | |||||
chrX:30715354
|
T | A | 1 | a0001c0001t0002g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.976-3184T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715354 | ||||||
chrX:30715552
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.976-2986A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715552 | ||||||
chrX:30715627
|
G | GA | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-2911_976-2910i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715627 | ||||||
chrX:30715637
|
G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp1 HG02293.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2901G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715637 | ||||||
chrX:30715745
|
T | TG | 1 | a0001c0001t0003g0161 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.976-2793_976-2792i others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715745 | ||||||
chrX:30715752
|
T | C | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.976-2786T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715752 | ||||||
chrX:30715796
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.976-2742G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30715796 | ||||||
chrX:30716251
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.976-2287G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716251 | ||||||
chrX:30716449
|
C | CA | 3 | a0001c0001t0004g0171a0001c0001t0004g0180a0001c0001t0011g0181 | 3 | HG02451.hp1 HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.976-2080dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30716449 | |||||
chrX:30716544
|
CT | C | 1 | a0001c0001t0002g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.976-1989delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30716544 | |||||
chrX:30716627
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.976-1911A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716627 | ||||||
chrX:30716771
|
T | TA | 3 | a0001c0001t0004g0184a0001c0001t0011g0007a0001c0001t0015g0106 | 3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.976-1765dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30716771 | |||||
chrX:30716832
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(195): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.976-1706C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716832 | ||||||
chrX:30716886
|
C | T | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976-1652C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30716886 | ||||||
chrX:30717128
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.976-1410T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717128 | ||||||
chrX:30717227
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.976-1311T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717227 | ||||||
chrX:30717291
|
C | CT | 4 | a0001c0001t0001g0080a0001c0001t0002g0168a0001c0001t0002g0275others(1): Show | 4 | HG01884.hp2 HG03669.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.976-1236dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30717291 | |||||
chrX:30717424
|
C | G | 1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.976-1114C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717424 | ||||||
chrX:30717476
|
A | C | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.976-1062A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717476 | ||||||
chrX:30717536
|
T | TTG | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-1000_976-999du others(3): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30717536 | |||||
chrX:30717575
|
A | AT | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-962dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30717575 | |||||
chrX:30717728
|
G | GA | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-809dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30717728 | |||||
chrX:30717777
|
A | AT | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-758dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30717777 | |||||
chrX:30717810
|
T | TG | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-728_976-727ins others(1): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30717810 | ||||||
chrX:30718065
|
T | TC | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-473_976-472ins others(1): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30718065 | ||||||
chrX:30718167
|
A | T | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-371A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30718167 | ||||||
chrX:30718262
|
AAGAAGCA others(4): Show |
A | 1 | a0001c0001t0001g0061 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.976-275_976-265del others(11): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | chrX | 30718262 | ||||||
chrX:30718403
|
G | GT | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.976-132dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | 30718403 | |||||
chrX:30718638
|
G | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+22G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30718638 | ||||||
chrX:30718687
|
T | TA | 1 | a0001c0001t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1054+74dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 30718687 | |||||
chrX:30719092
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(191): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1055-327T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719092 | ||||||
chrX:30719162
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-257G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719162 | ||||||
chrX:30719225
|
G | A | 2 | a0001c0001t0004g0174a0001c0001t0023g0173 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1055-194G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719225 | ||||||
chrX:30719278
|
G | A | 1 | a0001c0001t0009g0115 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1055-141G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719278 | ||||||
chrX:30719284
|
A | G | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1055-135A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719284 | ||||||
chrX:30719355
|
G | T | 1 | a0001c0001t0003g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-64G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 14/20 | chrX | 30719355 | ||||||
chrX:30719552
|
T | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1151+37T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 15/20 | chrX | 30719552 | ||||||
chrX:30719640
|
G | A | 1 | a0001c0001t0011g0007 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1151+125G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 15/20 | chrX | 30719640 | ||||||
chrX:30720245
|
T | TC | 1 | a0001c0001t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1236+155dupC | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | 30720245 | |||||
chrX:30720761
|
T | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+20T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 17/20 | chrX | 30720761 | ||||||
chrX:30721038
|
C | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0245 | 2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1501+43C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721038 | ||||||
chrX:30721125
|
G | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1501+130G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721125 | ||||||
chrX:30721176
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(86): Show | 92 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1501+181T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721176 | ||||||
chrX:30721244
|
A | G | 8 | a0001c0001t0004g0016a0001c0001t0004g0172a0001c0001t0004g0174others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+249A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721244 | ||||||
chrX:30721296
|
C | CT | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(185): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1501+314dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721296 | |||||
chrX:30721296
|
C | CTT | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0169others(3): Show | 6 | HG01433.hp1 NA18946.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1501+313_1501+314d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721296 | |||||
chrX:30721377
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1501+382C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721377 | ||||||
chrX:30721448
|
C | T | 3 | a0001c0001t0004g0184a0001c0001t0011g0007a0001c0001t0014g0185 | 3 | HG02258.hp1 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1501+453C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721448 | ||||||
chrX:30721458
|
A | AT | 9 | a0001c0001t0001g0190a0001c0001t0002g0096a0001c0001t0003g0125others(6): Show | 9 | HG02080.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1501+482dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | |||||
chrX:30721458
|
AT | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(176): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1501+482delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | |||||
chrX:30721458
|
ATT | A | 4 | a0001c0001t0001g0278a0001c0001t0002g0021a0001c0001t0004g0180others(1): Show | 4 | HG02451.hp1 HG02809.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.1501+481_1501+482d others(4): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | |||||
chrX:30721458
|
ATTT | A | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1501+480_1501+482d others(5): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30721458 | |||||
chrX:30721506
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1501+511G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721506 | ||||||
chrX:30721508
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1501+513G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30721508 | ||||||
chrX:30722093
|
G | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0060others(9): Show | 12 | NA18941.hp1 NA18966.hp1 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1501+1098G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722093 | ||||||
chrX:30722334
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1501+1339A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722334 | ||||||
chrX:30722395
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(198): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1501+1400G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722395 | ||||||
chrX:30722780
|
A | G | 2 | a0001c0001t0003g0126a0001c0001t0003g0137 | 2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1502-1321A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30722780 | ||||||
chrX:30723116
|
C | T | 1 | a0001c0001t0002g0260 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1502-985C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723116 | ||||||
chrX:30723178
|
G | A | 4 | a0001c0001t0003g0130a0001c0001t0004g0171a0001c0001t0004g0180others(1): Show | 4 | HG02074.hp1 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-923G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723178 | ||||||
chrX:30723272
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1502-829G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723272 | ||||||
chrX:30723322
|
G | A | 1 | a0001c0001t0004g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1502-779G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723322 | ||||||
chrX:30723344
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1502-757G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723344 | ||||||
chrX:30723394
|
C | CA | 4 | a0001c0001t0002g0183a0001c0001t0004g0184a0001c0001t0011g0007others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-695dupA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30723394 | |||||
chrX:30723452
|
C | G | 1 | a0001c0001t0003g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1502-649C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723452 | ||||||
chrX:30723461
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1502-640G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723461 | ||||||
chrX:30723514
|
C | T | 2 | a0001c0001t0012g0110a0001c0001t0012g0164 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1502-587C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723514 | ||||||
chrX:30723562
|
A | G | 1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1502-539A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723562 | ||||||
chrX:30723611
|
T | TTTTG | 2 | a0001c0001t0002g0218a0001c0001t0002g0241 | 2 | HG00099.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1502-466_1502-463d others(6): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30723611 | |||||
chrX:30723611
|
TTTTGTTT others(1): Show |
T | 62 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 64 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1502-470_1502-463d others(10): Show |
GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chrX | 30723611 | |||||
chrX:30723839
|
A | C | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-262A>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 18/20 | chrX | 30723839 | ||||||
chrX:30724475
|
GA | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1582+305delA | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30724475 | |||||
chrX:30724574
|
T | G | 90 | a0001c0001t0001g0213a0001c0001t0001g0265a0001c0001t0002g0005others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1582+393T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724574 | ||||||
chrX:30724678
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1582+497G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724678 | ||||||
chrX:30724828
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0061 | 2 | NA18941.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1582+647G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724828 | ||||||
chrX:30724884
|
CT | C | 2 | a0001c0001t0003g0028a0001c0001t0016g0272 | 2 | HG03540.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1582+717delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30724884 | |||||
chrX:30724966
|
C | T | 6 | a0001c0001t0003g0113a0001c0001t0003g0121a0001c0001t0003g0128others(3): Show | 6 | HG01496.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1582+785C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724966 | ||||||
chrX:30724976
|
G | T | 4 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1582+795G>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30724976 | ||||||
chrX:30725473
|
T | A | 11 | a0001c0001t0005g0022a0001c0001t0005g0100a0001c0001t0005g0104others(8): Show | 11 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1582+1292T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725473 | ||||||
chrX:30725644
|
A | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(275): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1582+1463A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725644 | ||||||
chrX:30725857
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1583-1609C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725857 | ||||||
chrX:30725893
|
T | C | 1 | a0001c0001t0004g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1583-1573T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30725893 | ||||||
chrX:30726047
|
A | AT | 1 | a0001c0001t0004g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583-1415dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30726047 | |||||
chrX:30726072
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1583-1394A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726072 | ||||||
chrX:30726090
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0079 | 2 | HG02738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1583-1376C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726090 | ||||||
chrX:30726189
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1583-1277C>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726189 | ||||||
chrX:30726286
|
A | AT | 4 | a0001c0001t0001g0056a0001c0001t0001g0169a0001c0001t0003g0138others(1): Show | 4 | HG02258.hp1 NA18960.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1583-1162dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30726286 | |||||
chrX:30726286
|
AT | A | 9 | a0001c0001t0002g0155a0001c0001t0002g0214a0001c0001t0002g0236others(6): Show | 9 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1583-1162delT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 30726286 | |||||
chrX:30726437
|
G | A | 2 | a0001c0001t0004g0184a0001c0001t0011g0007 | 2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1583-1029G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726437 | ||||||
chrX:30726566
|
C | T | 1 | a0001c0001t0004g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1583-900C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 19/20 | chrX | 30726566 | ||||||
chrX:30727649
|
T | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0079 | 2 | HG02738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1669+97T>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727649 | ||||||
chrX:30727673
|
A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1669+121A>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727673 | ||||||
chrX:30727694
|
C | A | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1669+142C>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727694 | ||||||
chrX:30727749
|
T | A | 3 | a0001c0001t0004g0184a0001c0001t0011g0007a0001c0001t0015g0106 | 3 | HG02258.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1669+197T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30727749 | ||||||
chrX:30728024
|
A | G | 1 | a0001c0001t0014g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1669+472A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728024 | ||||||
chrX:30728042
|
C | T | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1669+490C>T | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728042 | ||||||
chrX:30728335
|
C | CT | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0014others(186): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1670-395dupT | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chrX | 30728335 | |||||
chrX:30728348
|
T | A | 1 | a0001c0004t0017g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1670-384T>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728348 | ||||||
chrX:30728384
|
A | G | 1 | a0001c0001t0003g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1670-348A>G | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728384 | ||||||
chrX:30728543
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1670-189G>A | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728543 | ||||||
chrX:30728616
|
T | C | 1 | a0001c0001t0009g0115 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1670-116T>C | GK | ENSG00000198814.14 | transcript | ENST00000427190.6 | protein_coding | 20/20 | chrX | 30728616 |