Item | Value |
---|---|
geneid | 84187 |
ensemblid | ENSG00000157600.12 |
hgncid | 26217 |
symbol | TMEM164 |
name | transmembrane protein 164 |
refseq_nuc | NM_032227.4 |
refseq_prot | NP_115603.2 |
ensembl_nuc | ENST00000372068.7 |
ensembl_prot | ENSP00000361138.2 |
mane_status | MANE Select |
chr | chrX |
start | 110003114 |
end | 110177788 |
strand | + |
ver | v1.2 |
region | chrX:110003114-110177788 |
region5000 | chrX:109998114-110182788 |
regionname0 | TMEM164_chrX_110003114_110177788 |
regionname5000 | TMEM164_chrX_109998114_110182788 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 297 | 196 | 58 | 39 | 73 | 5 | 19 | 54 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0002 | 0/0 | 297 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0003 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 894 | 196 | 58 | 39 | 73 | 5 | 19 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 | |
c0002 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 | |
c0003 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4676 | 73 | 1 | 13 | 50 | 0 | 8 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0002 | 1/0 | 4677 | 37 | 1 | 16 | 6 | 4 | 9 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0003 | 0/0 | 4677 | 29 | 25 | 3 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0004 | 0/0 | 4677 | 12 | 11 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0005 | 0/0 | 4677 | 6 | 0 | 2 | 4 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0006 | 0/0 | 4676 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0007 | 0/0 | 4677 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0008 | 0/0 | 4676 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0009 | 0/0 | 4677 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0010 | 0/0 | 4677 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0011 | 0/0 | 4677 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0012 | 0/0 | 4678 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0013 | 0/0 | 4678 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0014 | 0/0 | 4677 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0015 | 0/0 | 4675 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0016 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0017 | 0/0 | 4680 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0018 | 0/0 | 4676 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0019 | 0/0 | 4677 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0020 | 0/0 | 4675 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0021 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0022 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0023 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0024 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0025 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0026 | 0/0 | 4673 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0027 | 0/0 | 4677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
t0028 | 0/0 | 4676 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 894 | 196 | 58 | 39 | 73 | 5 | 19 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 | |
a0002c0002 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 | |
a0003c0003 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5569 | 72 | 1 | 13 | 50 | 0 | 7 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0002 | 1/0 | 5570 | 37 | 1 | 16 | 6 | 4 | 9 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0003 | 0/0 | 5570 | 29 | 25 | 3 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0004 | 0/0 | 5570 | 12 | 11 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0005 | 0/0 | 5570 | 6 | 0 | 2 | 4 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0006 | 0/0 | 5569 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0007 | 0/0 | 5570 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0008 | 0/0 | 5569 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0009 | 0/0 | 5570 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0010 | 0/0 | 5570 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0011 | 0/0 | 5570 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0012 | 0/0 | 5571 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0013 | 0/0 | 5571 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0014 | 0/0 | 5570 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0015 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0017 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0018 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0019 | 0/0 | 5570 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0020 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0021 | 0/0 | 5570 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0022 | 0/0 | 5570 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0023 | 0/0 | 5571 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0024 | 0/0 | 5570 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0025 | 0/0 | 5570 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0026 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0027 | 0/0 | 5570 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0001c0001t0028 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0002c0002t0001 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
a0003c0003t0016 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | copy fasta | chrX | 109998114 | 110182788 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0015g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0017g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0018g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0019g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0020g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0021g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0022g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0023g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0024g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0026g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0027g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0001c0001t0028g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
a0003c0003t0016g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0154 | EUR | GBR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0082 | EUR | FIN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00408 | hp2 | a0001 | c0001 | t0013 | g0135 | EAS | CHS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00609 | hp1 | a0001 | c0001 | t0020 | g0169 | EAS | CHS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0153 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0035 | AMR | PUR | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01346 | hp2 | a0001 | c0001 | t0026 | g0141 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | IBS | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0030 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0033 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02040 | hp1 | a0001 | c0001 | t0018 | g0191 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02055 | hp1 | a0001 | c0001 | t0023 | g0096 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02145 | hp1 | a0001 | c0001 | t0028 | g0042 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CDX | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0031 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0143 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02717 | hp1 | a0001 | c0001 | t0027 | g0084 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0139 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0090 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03209 | hp1 | a0001 | c0001 | t0022 | g0002 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03453 | hp1 | a0001 | c0001 | t0021 | g0017 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0047 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03669 | hp2 | a0001 | c0001 | t0019 | g0163 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | STU | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0101 | SAS | STU | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | YRI | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18906 | hp1 | a0001 | c0001 | t0024 | g0001 | AFR | YRI | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18989 | hp1 | a0001 | c0001 | t0017 | g0179 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19011 | hp1 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | LWK | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | LWK | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | LWK | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19072 | hp1 | a0003 | c0003 | t0016 | g0142 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19082 | hp1 | a0001 | c0001 | t0015 | g0196 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02109 | hp1 | a0001 | c0001 | t0025 | g0005 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02109 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | USA | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | USA | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | USA | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0091 | AFR | LWK | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0050 | REF | REF | TMEM164_chrX_109998114_110182788 | TMEM164 | chrX | 109998114 | 110182788 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:110067386 | G | A | 1 | a0002 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.430G>A | p.Val144Ile | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/7 | 769/5570 | 430/894 | 144/297 | chrX | 110067386 | ||
chrX:110171484 | CT | C | 1 | a0003 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.655delT | p.Tyr219fs | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/7 | 994/5570 | 655/894 | 219/297 | INFO_REALIGN_3_PRIME | chrX | 110171484 |
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 |
---|
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:110173460 | AT | A | 10 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(7): Show | 93 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*23delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 23 | INFO_REALIGN_3_PRIME | chrX | 110173460 | ||||
chrX:110173460 | ATT | A | 1 | a0001c0001t0015 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22_*23delTT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 22 | INFO_REALIGN_3_PRIME | chrX | 110173460 | ||||
chrX:110173563 | AT | A | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*115delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 115 | INFO_REALIGN_3_PRIME | chrX | 110173563 | ||||
chrX:110173609 | T | C | 9 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(6): Show | 28 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*158T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 158 | chrX | 110173609 | |||||
chrX:110173960 | AG | A | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 512 | INFO_REALIGN_3_PRIME | chrX | 110173960 | ||||
chrX:110174094 | GC | G | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 646 | INFO_REALIGN_3_PRIME | chrX | 110174094 | ||||
chrX:110174357 | C | G | 4 | a0001c0001t0004a0001c0001t0011a0001c0001t0023others(1): Show | 16 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*906C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 906 | chrX | 110174357 | |||||
chrX:110174375 | C | CCT | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924_*925insCT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 925 | chrX | 110174375 | |||||
chrX:110174376 | T | C | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 925 | chrX | 110174376 | |||||
chrX:110174376 | T | TC | 5 | a0001c0001t0005a0001c0001t0012a0001c0001t0013others(2): Show | 12 | HG00408.hp2 HG00642.hp1 HG01099.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*931dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 932 | INFO_REALIGN_3_PRIME | chrX | 110174376 | ||||
chrX:110174376 | TC | T | 1 | a0001c0001t0020 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 931 | INFO_REALIGN_3_PRIME | chrX | 110174376 | ||||
chrX:110174968 | AT | A | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1521 | INFO_REALIGN_3_PRIME | chrX | 110174968 | ||||
chrX:110174994 | C | A | 1 | a0001c0001t0009 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1543C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1543 | chrX | 110174994 | |||||
chrX:110175049 | TC | T | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1602delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1602 | INFO_REALIGN_3_PRIME | chrX | 110175049 | ||||
chrX:110175127 | GT | G | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1681 | INFO_REALIGN_3_PRIME | chrX | 110175127 | ||||
chrX:110175139 | C | CT | 1 | a0003c0003t0016 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1692 | INFO_REALIGN_3_PRIME | chrX | 110175139 | ||||
chrX:110175376 | G | A | 4 | a0001c0001t0007a0001c0001t0009a0001c0001t0021others(1): Show | 9 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1925G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 1925 | chrX | 110175376 | |||||
chrX:110175563 | A | AC | 1 | a0001c0001t0019 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 2117 | INFO_REALIGN_3_PRIME | chrX | 110175563 | ||||
chrX:110175661 | GAGGA | G | 1 | a0001c0001t0026 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2217_*2220delGAAG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 2217 | INFO_REALIGN_3_PRIME | chrX | 110175661 | ||||
chrX:110175937 | G | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 155 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*2486G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 2486 | chrX | 110175937 | |||||
chrX:110176417 | A | G | 1 | a0001c0001t0011 | 2 | HG02258.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2966A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 2966 | chrX | 110176417 | |||||
chrX:110176434 | C | T | 1 | a0001c0001t0018 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2983C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 2983 | chrX | 110176434 | |||||
chrX:110176538 | C | T | 1 | a0001c0001t0006 | 6 | NA18959.hp1 NA18962.hp1 NA18966.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3087C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3087 | chrX | 110176538 | |||||
chrX:110176576 | T | C | 1 | a0001c0001t0027 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3125 | chrX | 110176576 | |||||
chrX:110176684 | G | T | 1 | a0001c0001t0014 | 2 | HG01884.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3233G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3233 | chrX | 110176684 | |||||
chrX:110176807 | C | A | 5 | a0001c0001t0007a0001c0001t0009a0001c0001t0022others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3356C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3356 | chrX | 110176807 | |||||
chrX:110176923 | A | AG | 1 | a0001c0001t0017 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3475dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3476 | INFO_REALIGN_3_PRIME | chrX | 110176923 | ||||
chrX:110177010 | G | GC | 1 | a0001c0001t0017 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3559_*3560insC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3560 | chrX | 110177010 | |||||
chrX:110177012 | C | G | 1 | a0001c0001t0017 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3561C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3561 | chrX | 110177012 | |||||
chrX:110177207 | G | GT | 1 | a0001c0001t0017 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3760dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3761 | INFO_REALIGN_3_PRIME | chrX | 110177207 | ||||
chrX:110177435 | AC | A | 1 | a0001c0001t0028 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3989delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 7/7 | 3989 | INFO_REALIGN_3_PRIME | chrX | 110177435 |
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:110003377 | C | T | 96 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0111others(93): Show | 96 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-274-124C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 1/6 | chrX | 110003377 | ||||||
chrX:110003469 | C | CT | 3 | a0001c0001t0001g0102a0001c0001t0005g0100a0001c0001t0008g0101 | 3 | HG04115.hp1 NA19000.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-274-18dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 110003469 | |||||
chrX:110003469 | CT | C | 117 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0111others(114): Show | 117 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-274-18delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 110003469 | |||||
chrX:110003469 | CTT | C | 2 | a0001c0001t0022g0002a0001c0001t0024g0001 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-274-19_-274-18del others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 110003469 | |||||
chrX:110005021 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.390+857C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005021 | ||||||
chrX:110005251 | C | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+1087C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005251 | ||||||
chrX:110005286 | C | T | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+1122C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005286 | ||||||
chrX:110005307 | G | A | 123 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0111others(120): Show | 123 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.390+1143G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005307 | ||||||
chrX:110005425 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.390+1261A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005425 | ||||||
chrX:110005672 | C | T | 4 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+1508C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005672 | ||||||
chrX:110005791 | G | C | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.390+1627G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110005791 | ||||||
chrX:110006240 | T | C | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+2076T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110006240 | ||||||
chrX:110006639 | G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.390+2475G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110006639 | ||||||
chrX:110006672 | C | T | 2 | a0001c0001t0003g0018a0001c0001t0021g0017 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+2508C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110006672 | ||||||
chrX:110006754 | GCCT | G | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.390+2591_390+2593d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110006754 | ||||||
chrX:110007344 | G | A | 113 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.390+3180G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110007344 | ||||||
chrX:110008006 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.390+3842C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008006 | ||||||
chrX:110008126 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+3962T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008126 | ||||||
chrX:110008136 | T | A | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+3972T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008136 | ||||||
chrX:110008277 | A | C | 2 | a0001c0001t0001g0197a0001c0001t0015g0196 | 2 | NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.390+4113A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008277 | ||||||
chrX:110008318 | C | G | 6 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+4154C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008318 | ||||||
chrX:110008385 | C | T | 113 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.390+4221C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110008385 | ||||||
chrX:110009279 | A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 4 | HG02015.hp1 NA18984.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+5115A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009279 | ||||||
chrX:110009350 | C | G | 1 | a0001c0001t0003g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390+5186C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009350 | ||||||
chrX:110009500 | TCCA | T | 44 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(41): Show | 44 | HG00280.hp1 HG00408.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.390+5340_390+5342d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110009500 | |||||
chrX:110009731 | A | G | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0011g0026 | 3 | HG02258.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.390+5567A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009731 | ||||||
chrX:110009866 | G | A | 1 | a0001c0001t0014g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.390+5702G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009866 | ||||||
chrX:110009888 | G | A | 113 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.390+5724G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009888 | ||||||
chrX:110009907 | C | T | 112 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0111others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.390+5743C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110009907 | ||||||
chrX:110009992 | C | CA | 4 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0002g0056others(1): Show | 4 | HG01261.hp1 HG01433.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+5844dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110009992 | |||||
chrX:110009992 | CA | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(2): Show | 5 | HG03239.hp2 HG03492.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+5844delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110009992 | |||||
chrX:110009992 | CAAA | C | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.390+5842_390+5844d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110009992 | |||||
chrX:110010000 | A | T | 1 | a0001c0001t0018g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.390+5836A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110010000 | ||||||
chrX:110010366 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.390+6202T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110010366 | ||||||
chrX:110010441 | G | T | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.390+6277G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110010441 | ||||||
chrX:110010541 | A | G | 113 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(110): Show | 113 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.390+6377A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110010541 | ||||||
chrX:110010766 | G | C | 4 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+6602G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110010766 | ||||||
chrX:110011189 | C | CA | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+7035dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110011189 | |||||
chrX:110011197 | AAAG | A | 1 | a0001c0001t0004g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.390+7040_390+7042d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110011197 | |||||
chrX:110011447 | C | T | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+7283C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011447 | ||||||
chrX:110011561 | A | G | 10 | a0001c0001t0002g0015a0001c0001t0003g0012a0001c0001t0003g0018others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+7397A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011561 | ||||||
chrX:110011588 | T | C | 2 | a0001c0001t0010g0010a0001c0001t0011g0009 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.390+7424T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011588 | ||||||
chrX:110011623 | G | A | 7 | a0001c0001t0003g0036a0001c0001t0004g0034a0001c0001t0004g0054others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+7459G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011623 | ||||||
chrX:110011728 | G | A | 4 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+7564G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011728 | ||||||
chrX:110011775 | G | A | 2 | a0001c0001t0001g0197a0001c0001t0015g0196 | 2 | NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.390+7611G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110011775 | ||||||
chrX:110012058 | A | G | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+7894A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110012058 | ||||||
chrX:110012081 | C | G | 175 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(172): Show | 175 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.390+7917C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110012081 | ||||||
chrX:110012329 | T | C | 10 | a0001c0001t0002g0015a0001c0001t0003g0012a0001c0001t0003g0018others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+8165T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110012329 | ||||||
chrX:110012628 | C | T | 7 | a0001c0001t0003g0036a0001c0001t0004g0034a0001c0001t0004g0054others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+8464C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110012628 | ||||||
chrX:110012734 | G | A | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.390+8570G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110012734 | ||||||
chrX:110013435 | G | C | 1 | a0001c0001t0011g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390+9271G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110013435 | ||||||
chrX:110013624 | G | A | 1 | a0001c0001t0004g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+9460G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110013624 | ||||||
chrX:110013810 | A | G | 3 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0023g0096 | 3 | HG02055.hp1 HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.390+9646A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110013810 | ||||||
chrX:110014022 | T | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0111a0001c0001t0002g0109others(4): Show | 7 | HG02155.hp1 NA18961.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+9858T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110014022 | ||||||
chrX:110014050 | AGTT | A | 2 | a0001c0001t0002g0112a0001c0001t0003g0113 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.390+9892_390+9894d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014050 | |||||
chrX:110014142 | A | AATG | 102 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.390+9995_390+9997d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014142 | |||||
chrX:110014234 | C | T | 1 | a0001c0001t0011g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390+10070C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110014234 | ||||||
chrX:110014295 | A | C | 1 | a0001c0001t0018g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.390+10131A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110014295 | ||||||
chrX:110014669 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.390+10505G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110014669 | ||||||
chrX:110014724 | G | GT | 3 | a0001c0001t0003g0025a0001c0001t0003g0028a0001c0001t0011g0026 | 3 | HG02257.hp2 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.390+10571dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014724 | |||||
chrX:110014744 | C | CT | 3 | a0001c0001t0001g0097a0001c0001t0003g0052a0001c0001t0003g0053 | 3 | HG02622.hp2 HG03486.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.390+10603dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014744 | C | CTTT | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.390+10601_390+1060 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014744 | C | CTTTT | 1 | a0001c0001t0023g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.390+10600_390+1060 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014744 | CT | C | 20 | a0001c0001t0002g0015a0001c0001t0003g0012a0001c0001t0003g0018others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.390+10603delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014744 | CTT | C | 102 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.390+10602_390+1060 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014744 | CTTT | C | 10 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(7): Show | 10 | HG01167.hp1 HG01943.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.390+10601_390+1060 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014744 | |||||
chrX:110014919 | GAGA | G | 10 | a0001c0001t0002g0015a0001c0001t0003g0012a0001c0001t0003g0018others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+10758_390+1076 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110014919 | |||||
chrX:110015021 | T | C | 1 | a0001c0001t0004g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.390+10857T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015021 | ||||||
chrX:110015461 | T | A | 1 | a0001c0001t0005g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.390+11297T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015461 | ||||||
chrX:110015501 | G | A | 110 | a0001c0001t0001g0029a0001c0001t0001g0105a0001c0001t0001g0107others(107): Show | 110 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.390+11337G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015501 | ||||||
chrX:110015550 | A | AGT | 4 | a0001c0001t0001g0029a0001c0001t0003g0055a0001c0001t0005g0092others(1): Show | 4 | HG02132.hp1 HG03130.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+11416_390+1141 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015550 | |||||
chrX:110015550 | A | AGTGT | 6 | a0001c0001t0002g0015a0001c0001t0002g0184a0001c0001t0003g0012others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+11414_390+1141 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015550 | |||||
chrX:110015550 | AGT | A | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0003g0004others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.390+11416_390+1141 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015550 | |||||
chrX:110015550 | AGTGT | A | 2 | a0001c0001t0001g0122a0001c0001t0007g0006 | 2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.390+11414_390+1141 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015550 | |||||
chrX:110015550 | AGTGTGT | A | 1 | a0001c0001t0002g0121 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.390+11412_390+1141 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015550 | |||||
chrX:110015580 | T | C | 1 | a0001c0001t0003g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.390+11416T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015580 | ||||||
chrX:110015580 | T | TGC | 8 | a0001c0001t0003g0036a0001c0001t0004g0008a0001c0001t0004g0034others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+11421_390+1142 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110015580 | |||||
chrX:110015715 | G | T | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+11551G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015715 | ||||||
chrX:110015738 | G | C | 11 | a0001c0001t0003g0004a0001c0001t0003g0020a0001c0001t0003g0021others(8): Show | 11 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.390+11574G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015738 | ||||||
chrX:110015768 | T | C | 6 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(3): Show | 6 | HG01891.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+11604T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110015768 | ||||||
chrX:110016070 | G | C | 169 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.390+11906G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016070 | ||||||
chrX:110016132 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.390+11968C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016132 | ||||||
chrX:110016398 | C | A | 2 | a0001c0001t0009g0031a0001c0001t0009g0032 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.390+12234C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016398 | ||||||
chrX:110016450 | G | A | 155 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.390+12286G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016450 | ||||||
chrX:110016601 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.390+12437A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016601 | ||||||
chrX:110016643 | G | GT | 2 | a0001c0001t0003g0018a0001c0001t0021g0017 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.390+12485dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110016643 | |||||
chrX:110016666 | TG | T | 1 | a0001c0001t0001g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.390+12503delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016666 | ||||||
chrX:110016667 | G | T | 132 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0001g0060others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.390+12503G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016667 | ||||||
chrX:110016779 | C | T | 2 | a0001c0001t0004g0007a0001c0001t0025g0005 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.390+12615C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016779 | ||||||
chrX:110016888 | C | T | 6 | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+12724C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110016888 | ||||||
chrX:110017121 | C | G | 133 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0001g0060others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.390+12957C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017121 | ||||||
chrX:110017349 | T | C | 1 | a0001c0001t0014g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.390+13185T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017349 | ||||||
chrX:110017405 | C | CCTTCCTT others(5): Show |
2 | a0001c0001t0002g0015a0001c0001t0004g0016 | 2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.390+13244_390+1324 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTCCTT others(21): Show |
2 | a0001c0001t0004g0094a0001c0001t0023g0096 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.390+13244_390+1324 others(32): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.390+13244_390+1324 others(36): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTCCTT others(29): Show |
1 | a0001c0001t0004g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+13244_390+1324 others(40): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTT | 3 | a0001c0001t0003g0012a0001c0001t0004g0008a0001c0001t0007g0013 | 3 | HG02451.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.390+13280_390+1328 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(1): Show |
1 | a0001c0001t0012g0090 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.390+13276_390+1328 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.390+13254_390+1325 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(13): Show |
6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0125others(3): Show | 6 | HG01258.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+13254_390+1325 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(17): Show |
28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(25): Show | 28 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.390+13254_390+1325 others(28): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(21): Show |
39 | a0001c0001t0001g0079a0001c0001t0001g0107a0001c0001t0001g0114others(36): Show | 39 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.390+13254_390+1325 others(32): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(25): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0102a0001c0001t0001g0164others(6): Show | 9 | HG00280.hp1 HG02132.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+13254_390+1325 others(36): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(29): Show |
8 | a0001c0001t0001g0120a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG01168.hp1 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+13254_390+1325 others(40): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(33): Show |
2 | a0001c0001t0003g0113a0001c0001t0017g0179 | 2 | HG01168.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.390+13254_390+1325 others(44): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(37): Show |
1 | a0001c0001t0005g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.390+13254_390+1325 others(48): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(23): Show |
1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.390+13256_390+1325 others(34): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(9): Show |
2 | a0001c0001t0003g0025a0001c0001t0004g0011 | 2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.390+13268_390+1328 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.390+13264_390+1328 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017405 | C | CCTTTCTT others(17): Show |
1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.390+13260_390+1328 others(28): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017405 | |||||
chrX:110017407 | T | TTTCTTTC others(5): Show |
1 | a0001c0001t0002g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.390+13254_390+1325 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017407 | |||||
chrX:110017411 | T | TTTCTTTC others(1): Show |
1 | a0001c0001t0004g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+13254_390+1325 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017411 | |||||
chrX:110017415 | T | TTTCC | 3 | a0001c0001t0002g0085a0001c0001t0003g0027a0001c0001t0005g0175 | 3 | HG02723.hp1 NA19009.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.390+13254_390+1325 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017415 | |||||
chrX:110017419 | T | C | 72 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058others(69): Show | 72 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.390+13255T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017419 | ||||||
chrX:110017442 | CTT | C | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390+13280_390+1328 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017442 | |||||
chrX:110017444 | T | C | 89 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0001g0060others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.390+13280T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017444 | ||||||
chrX:110017444 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.390+13283_390+1328 others(18): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(9): Show |
1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390+13283_390+1328 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(11): Show |
7 | a0001c0001t0001g0183a0001c0001t0003g0020a0001c0001t0003g0024others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(22): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+13283_390+1328 others(26): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(15): Show |
14 | a0001c0001t0001g0058a0001c0001t0001g0088a0001c0001t0001g0099others(11): Show | 14 | HG00408.hp2 HG00673.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(26): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(19): Show |
1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.390+13283_390+1328 others(30): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(19): Show |
7 | a0001c0001t0001g0122a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00735.hp2 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(30): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(23): Show |
9 | a0001c0001t0001g0105a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG00609.hp1 HG00735.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(34): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0001g0178 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.390+13283_390+1328 others(38): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(31): Show |
4 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0110others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(42): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | T | TTCTTTCT others(31): Show |
2 | a0001c0001t0001g0181a0001c0001t0003g0062 | 2 | HG01978.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.390+13283_390+1328 others(42): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | TTCTCTCT others(1): Show |
T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+13292_390+1329 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017444 | TTCTCTCT others(5): Show |
T | 1 | a0001c0001t0025g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+13288_390+1329 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017444 | |||||
chrX:110017446 | C | CTT | 6 | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+13283_390+1328 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017446 | |||||
chrX:110017446 | C | CTTTCTTT others(11): Show |
1 | a0001c0001t0004g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390+13283_390+1328 others(22): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017446 | |||||
chrX:110017448 | C | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(26): Show | 29 | HG01346.hp2 HG02027.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.390+13284C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017448 | ||||||
chrX:110017452 | C | T | 28 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(25): Show | 28 | HG01346.hp2 HG02027.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.390+13288C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017452 | ||||||
chrX:110017456 | C | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(26): Show | 29 | HG01346.hp2 HG02027.hp1 HG02559.hp2 others(26): Show |
intron_variant | MODIFIER | c.390+13292C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017456 | ||||||
chrX:110017460 | C | T | 30 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(27): Show | 30 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.390+13296C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017460 | ||||||
chrX:110017464 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.390+13300T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017464 | ||||||
chrX:110017466 | CTTTCCT | C | 2 | a0001c0001t0001g0040a0001c0001t0003g0038 | 2 | HG02559.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.390+13304_390+1330 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017466 | |||||
chrX:110017468 | T | C | 7 | a0001c0001t0001g0073a0001c0001t0003g0021a0001c0001t0003g0023others(4): Show | 7 | HG02572.hp1 HG02965.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+13304T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017468 | ||||||
chrX:110017470 | C | CTTT | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.390+13306_390+1330 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017470 | ||||||
chrX:110017470 | CCT | C | 8 | a0001c0001t0001g0097a0001c0001t0003g0021a0001c0001t0003g0023others(5): Show | 8 | HG02572.hp1 HG02965.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+13307_390+1330 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017470 | ||||||
chrX:110017471 | C | T | 19 | a0001c0001t0001g0073a0001c0001t0001g0173a0001c0001t0001g0180others(16): Show | 19 | HG01346.hp2 HG02109.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.390+13307C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017471 | ||||||
chrX:110017472 | T | C | 6 | a0001c0001t0001g0073a0001c0001t0003g0022a0001c0001t0003g0046others(3): Show | 6 | HG01346.hp2 HG02630.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+13308T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017472 | ||||||
chrX:110017472 | T | TTCCC | 1 | a0001c0001t0009g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.390+13348_390+1335 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017472 | |||||
chrX:110017472 | T | TTCTTTCT others(23): Show |
1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.390+13310_390+1331 others(34): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017472 | |||||
chrX:110017472 | TTCCC | T | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+13348_390+1335 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017472 | |||||
chrX:110017472 | TTCCCTCC others(5): Show |
T | 2 | a0001c0001t0002g0015a0001c0001t0003g0028 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.390+13340_390+1335 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017472 | |||||
chrX:110017474 | C | CTTTCTTT others(18): Show |
1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.390+13310_390+1331 others(29): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017474 | ||||||
chrX:110017475 | C | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(26): Show | 29 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.390+13311C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017475 | ||||||
chrX:110017476 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.390+13312C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017476 | ||||||
chrX:110017479 | C | T | 30 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(27): Show | 30 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.390+13315C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017479 | ||||||
chrX:110017480 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.390+13316C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017480 | ||||||
chrX:110017483 | C | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(26): Show | 29 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.390+13319C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017483 | ||||||
chrX:110017484 | C | CTCTCTCT others(10): Show |
1 | a0001c0001t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.390+13322_390+1332 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017484 | |||||
chrX:110017484 | C | CTCTCTCT others(8): Show |
1 | a0001c0001t0005g0175 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.390+13322_390+1332 others(19): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017484 | |||||
chrX:110017484 | C | CTCTCTCT others(6): Show |
3 | a0001c0001t0006g0140a0001c0001t0013g0139a0001c0001t0026g0141 | 3 | HG01346.hp2 HG02738.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.390+13322_390+1332 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017484 | |||||
chrX:110017484 | C | T | 2 | a0001c0001t0001g0180a0001c0001t0003g0004 | 2 | NA18974.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390+13320C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017484 | ||||||
chrX:110017487 | C | T | 24 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(21): Show | 24 | HG02027.hp1 HG02109.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.390+13323C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017487 | ||||||
chrX:110017488 | C | CTT | 2 | a0001c0001t0003g0022a0001c0001t0003g0046 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.390+13325_390+1332 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017488 | |||||
chrX:110017488 | C | T | 14 | a0001c0001t0001g0073a0001c0001t0002g0085a0001c0001t0003g0004others(11): Show | 14 | HG01346.hp2 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+13324C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017488 | ||||||
chrX:110017490 | C | CT | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.390+13326_390+1332 others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017490 | ||||||
chrX:110017491 | C | T | 22 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(19): Show | 22 | HG02109.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.390+13327C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017491 | ||||||
chrX:110017492 | C | CTCTCTTT others(3): Show |
1 | a0001c0001t0014g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.390+13330_390+1333 others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017492 | |||||
chrX:110017492 | C | CTT | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.390+13329_390+1333 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017492 | |||||
chrX:110017492 | C | CTTTCTT | 5 | a0001c0001t0003g0027a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02723.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+13329_390+1333 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017492 | |||||
chrX:110017492 | C | T | 17 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(14): Show | 17 | HG02027.hp1 HG02109.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.390+13328C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017492 | ||||||
chrX:110017495 | C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0097a0001c0001t0001g0124others(4): Show | 7 | HG02027.hp1 HG02109.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+13331C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017495 | ||||||
chrX:110017496 | C | T | 23 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(20): Show | 23 | HG02027.hp1 HG02109.hp1 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.390+13332C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017496 | ||||||
chrX:110017496 | CTCCCTCC others(25): Show |
C | 1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.390+13336_390+1336 others(36): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017496 | |||||
chrX:110017500 | C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0097a0001c0001t0001g0124others(4): Show | 7 | HG02027.hp1 HG02109.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+13336C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017500 | ||||||
chrX:110017500 | CTCCCTCC others(9): Show |
C | 3 | a0001c0001t0004g0016a0001c0001t0004g0094a0001c0001t0004g0095 | 3 | HG02486.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.390+13340_390+1335 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017500 | |||||
chrX:110017500 | CTCCCTCC others(13): Show |
C | 3 | a0001c0001t0001g0177a0001c0001t0023g0096a0001c0001t0027g0084 | 3 | HG02055.hp1 HG02717.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.390+13340_390+1335 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017500 | |||||
chrX:110017500 | CTCCCTCC others(21): Show |
C | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.390+13340_390+1336 others(32): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017500 | |||||
chrX:110017504 | CTCCCTCC others(5): Show |
C | 20 | a0001c0001t0001g0029a0001c0001t0001g0120a0001c0001t0001g0126others(17): Show | 20 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.390+13344_390+1335 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017504 | |||||
chrX:110017504 | CTCCCTCC others(9): Show |
C | 101 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.390+13344_390+1335 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017504 | |||||
chrX:110017504 | CTCCCTCC others(13): Show |
C | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0002g0056others(6): Show | 9 | HG01358.hp1 HG01433.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.390+13344_390+1336 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017504 | |||||
chrX:110017504 | CTCCCTCC others(17): Show |
C | 4 | a0001c0001t0003g0020a0001c0001t0003g0024a0001c0001t0004g0045others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+13344_390+1336 others(28): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017504 | |||||
chrX:110017508 | CTCCCTCC others(5): Show |
C | 3 | a0001c0001t0003g0052a0001c0001t0003g0064a0001c0001t0021g0017 | 3 | HG02622.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.390+13348_390+1335 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017508 | |||||
chrX:110017508 | CTCCCTCC others(9): Show |
C | 5 | a0001c0001t0002g0184a0001c0001t0003g0018a0001c0001t0007g0006others(2): Show | 5 | HG01106.hp1 HG02258.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+13348_390+1336 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017508 | |||||
chrX:110017508 | CTCCCTCC others(13): Show |
C | 3 | a0001c0001t0001g0058a0001c0001t0001g0099a0001c0001t0001g0183 | 3 | HG02602.hp1 NA18747.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.390+13348_390+1336 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017508 | |||||
chrX:110017512 | C | CTCCCTCC others(5): Show |
1 | a0001c0001t0009g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.390+13351_390+1335 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017512 | |||||
chrX:110017512 | C | CTCCCTCC others(1): Show |
1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.390+13351_390+1335 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017512 | |||||
chrX:110017512 | CTCCT | C | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.390+13394_390+1339 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017512 | |||||
chrX:110017512 | CTCCTTCC others(1): Show |
C | 2 | a0001c0001t0003g0012a0001c0001t0007g0013 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.390+13390_390+1339 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017512 | |||||
chrX:110017512 | CTCCTTCC others(9): Show |
C | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.390+13382_390+1339 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017512 | |||||
chrX:110017516 | T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(29): Show | 32 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+13352T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017516 | ||||||
chrX:110017520 | T | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(29): Show | 32 | HG01346.hp2 HG02027.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.390+13356T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017520 | ||||||
chrX:110017524 | T | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(23): Show | 26 | HG02027.hp1 HG02109.hp1 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.390+13360T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017524 | ||||||
chrX:110017528 | T | C | 21 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0097others(18): Show | 21 | HG02027.hp1 HG02559.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.390+13364T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017528 | ||||||
chrX:110017532 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.390+13368T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017532 | ||||||
chrX:110017572 | A | AT | 7 | a0001c0001t0003g0089a0001c0001t0004g0007a0001c0001t0004g0011others(4): Show | 7 | HG01106.hp1 HG01109.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+13422dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017572 | |||||
chrX:110017572 | AT | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0111a0001c0001t0001g0158others(3): Show | 6 | HG01069.hp1 HG01256.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+13422delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110017572 | |||||
chrX:110017592 | G | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058others(36): Show | 39 | HG01891.hp2 HG02027.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.390+13428G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017592 | ||||||
chrX:110017618 | G | A | 2 | a0001c0001t0003g0012a0001c0001t0007g0013 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.390+13454G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017618 | ||||||
chrX:110017694 | C | T | 6 | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+13530C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017694 | ||||||
chrX:110017799 | C | T | 1 | a0001c0001t0028g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390+13635C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017799 | ||||||
chrX:110017807 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.390+13643G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017807 | ||||||
chrX:110017848 | C | T | 38 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058others(35): Show | 38 | HG01891.hp2 HG02027.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.390+13684C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017848 | ||||||
chrX:110017861 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.390+13697G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110017861 | ||||||
chrX:110018098 | C | T | 182 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(179): Show | 182 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.390+13934C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110018098 | ||||||
chrX:110018117 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.390+13953C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110018117 | ||||||
chrX:110018242 | G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0117 | 2 | NA18960.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.390+14078G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110018242 | ||||||
chrX:110018537 | A | G | 3 | a0001c0001t0003g0012a0001c0001t0007g0013a0001c0001t0007g0014 | 3 | HG02647.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.390+14373A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110018537 | ||||||
chrX:110018578 | T | G | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+14414T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110018578 | ||||||
chrX:110018863 | GTGAATGT others(12): Show |
G | 4 | a0001c0001t0003g0089a0001c0001t0004g0011a0001c0001t0010g0091others(1): Show | 4 | HG01109.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+14719_390+1473 others(23): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110018863 | |||||
chrX:110019283 | A | C | 197 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(194): Show | 197 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.390+15119A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110019283 | ||||||
chrX:110019614 | AAC | A | 6 | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+15454_390+1545 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110019614 | |||||
chrX:110019861 | CT | C | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+15705delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110019861 | |||||
chrX:110020002 | T | G | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390+15838T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020002 | ||||||
chrX:110020207 | G | A | 1 | a0001c0001t0014g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.390+16043G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020207 | ||||||
chrX:110020216 | G | A | 3 | a0001c0001t0003g0089a0001c0001t0010g0091a0001c0001t0012g0090 | 3 | HG02559.hp1 HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.390+16052G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020216 | ||||||
chrX:110020252 | TA | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.390+16093delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020252 | |||||
chrX:110020389 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.390+16225A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020389 | ||||||
chrX:110020521 | T | C | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+16357T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020521 | ||||||
chrX:110020622 | C | T | 2 | a0001c0001t0004g0054a0001c0001t0024g0001 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.390+16458C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020622 | ||||||
chrX:110020930 | T | C | 6 | a0001c0001t0002g0015a0001c0001t0003g0028a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+16766T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020930 | ||||||
chrX:110020968 | T | TA | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0002g0076others(3): Show | 6 | HG01109.hp1 HG02083.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+16831dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020968 | |||||
chrX:110020968 | TA | T | 25 | a0001c0001t0001g0122a0001c0001t0001g0185a0001c0001t0002g0070others(22): Show | 25 | HG00280.hp1 HG01106.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.390+16831delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020968 | |||||
chrX:110020968 | TAA | T | 39 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(36): Show | 39 | HG01884.hp1 HG02015.hp1 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.390+16830_390+1683 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020968 | |||||
chrX:110020968 | TAAA | T | 92 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0097others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.390+16829_390+1683 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020968 | |||||
chrX:110020968 | TAAAA | T | 1 | a0001c0001t0001g0178 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.390+16828_390+1683 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110020968 | |||||
chrX:110020999 | C | G | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.390+16835C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110020999 | ||||||
chrX:110021023 | G | A | 6 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0126others(3): Show | 6 | HG02071.hp1 NA18953.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+16859G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021023 | ||||||
chrX:110021070 | A | G | 1 | a0001c0001t0005g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.390+16906A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021070 | ||||||
chrX:110021268 | C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02027.hp1 NA18940.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+17104C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021268 | ||||||
chrX:110021372 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.390+17208G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021372 | ||||||
chrX:110021379 | T | C | 196 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.390+17215T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021379 | ||||||
chrX:110021523 | A | ATG | 1 | a0001c0001t0003g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.390+17373_390+1737 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110021523 | |||||
chrX:110021523 | ATG | A | 4 | a0001c0001t0002g0063a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+17373_390+1737 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110021523 | |||||
chrX:110021645 | C | G | 43 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(40): Show | 43 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.390+17481C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021645 | ||||||
chrX:110021659 | A | G | 45 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(42): Show | 45 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.390+17495A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021659 | ||||||
chrX:110021676 | G | A | 1 | a0001c0001t0019g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.390+17512G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021676 | ||||||
chrX:110021782 | A | G | 1 | a0001c0001t0025g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+17618A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110021782 | ||||||
chrX:110022199 | A | ATG | 2 | a0001c0001t0001g0145a0001c0001t0005g0100 | 2 | HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.390+18055_390+1805 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110022199 | |||||
chrX:110022199 | A | ATGTGTGT others(9): Show |
5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+18041_390+1805 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110022199 | |||||
chrX:110022199 | A | ATGTGTGT others(17): Show |
2 | a0001c0001t0004g0007a0001c0001t0025g0005 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.390+18056_390+1805 others(28): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110022199 | |||||
chrX:110022199 | A | ATGTGTGT others(21): Show |
1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+18056_390+1805 others(32): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110022199 | |||||
chrX:110022244 | T | C | 5 | a0001c0001t0003g0027a0001c0001t0003g0043a0001c0001t0003g0044others(2): Show | 5 | HG02145.hp1 HG02723.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+18080T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110022244 | ||||||
chrX:110022269 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.390+18105C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110022269 | ||||||
chrX:110022306 | A | T | 102 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.390+18142A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110022306 | ||||||
chrX:110022315 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.390+18151G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110022315 | ||||||
chrX:110022468 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+18304C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110022468 | ||||||
chrX:110023324 | AT | A | 2 | a0001c0001t0004g0007a0001c0001t0025g0005 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.390+19171delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110023324 | |||||
chrX:110023437 | G | C | 1 | a0001c0001t0002g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.390+19273G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110023437 | ||||||
chrX:110024080 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.390+19916G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024080 | ||||||
chrX:110024087 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+19923T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024087 | ||||||
chrX:110024390 | T | TC | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+20227dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110024390 | |||||
chrX:110024395 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.390+20231C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024395 | ||||||
chrX:110024438 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+20274C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024438 | ||||||
chrX:110024520 | G | A | 1 | a0001c0001t0004g0037 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+20356G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024520 | ||||||
chrX:110024639 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.390+20475C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024639 | ||||||
chrX:110024739 | G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0174 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.390+20575G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024739 | ||||||
chrX:110024840 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.390+20676C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110024840 | ||||||
chrX:110024991 | G | GGGGTGTG others(1): Show |
1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+20828_390+2082 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110024991 | |||||
chrX:110024991 | G | GGT | 90 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.390+20854_390+2085 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110024991 | |||||
chrX:110024991 | G | GGTGT | 1 | a0001c0001t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.390+20852_390+2085 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110024991 | |||||
chrX:110024991 | GGT | G | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+20854_390+2085 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110024991 | |||||
chrX:110025150 | T | A | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.390+20986T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110025150 | ||||||
chrX:110025680 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.390+21516G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110025680 | ||||||
chrX:110025996 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+21832T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110025996 | ||||||
chrX:110026378 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.390+22214T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110026378 | ||||||
chrX:110026671 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.390+22507G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110026671 | ||||||
chrX:110026686 | A | G | 1 | a0001c0001t0012g0090 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.390+22522A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110026686 | ||||||
chrX:110026779 | G | C | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+22615G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110026779 | ||||||
chrX:110027356 | A | T | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+23192A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027356 | ||||||
chrX:110027476 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.390+23312G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027476 | ||||||
chrX:110027483 | C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0001g0189others(1): Show | 4 | HG02602.hp1 HG03239.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+23319C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027483 | ||||||
chrX:110027593 | C | G | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.390+23429C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027593 | ||||||
chrX:110027763 | A | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390+23599A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027763 | ||||||
chrX:110027902 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.390+23738A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027902 | ||||||
chrX:110027910 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390+23746T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110027910 | ||||||
chrX:110028153 | T | A | 1 | a0001c0001t0023g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.390+23989T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110028153 | ||||||
chrX:110028991 | CA | C | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+24831delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110028991 | |||||
chrX:110029182 | A | G | 2 | a0001c0001t0011g0026a0001c0001t0022g0002 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.390+25018A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110029182 | ||||||
chrX:110029558 | A | G | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+25394A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110029558 | ||||||
chrX:110029628 | C | T | 36 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0002g0041others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.390+25464C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110029628 | ||||||
chrX:110029943 | CT | C | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.390+25786delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110029943 | |||||
chrX:110029950 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.390+25786T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110029950 | ||||||
chrX:110030015 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+25851T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110030015 | ||||||
chrX:110030038 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+25874A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110030038 | ||||||
chrX:110030108 | G | GT | 3 | a0001c0001t0002g0136a0001c0001t0002g0167a0001c0001t0003g0036 | 3 | HG01978.hp2 HG02572.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.390+25973dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030108 | G | GTT | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.390+25972_390+2597 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030108 | GT | G | 121 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(118): Show | 121 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.390+25973delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030108 | GTT | G | 7 | a0001c0001t0002g0104a0001c0001t0002g0184a0001c0001t0003g0021others(4): Show | 7 | HG01169.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+25972_390+2597 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030108 | GTTT | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+25971_390+2597 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030108 | GTTTT | G | 4 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+25970_390+2597 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030108 | |||||
chrX:110030110 | T | G | 1 | a0001c0001t0003g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+25946T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110030110 | ||||||
chrX:110030111 | T | G | 4 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(1): Show | 4 | HG01891.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+25947T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110030111 | ||||||
chrX:110030415 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.390+26251C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110030415 | ||||||
chrX:110030421 | CT | C | 14 | a0001c0001t0001g0029a0001c0001t0002g0116a0001c0001t0003g0028others(11): Show | 14 | HG01243.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+26272delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030421 | |||||
chrX:110030810 | C | CA | 1 | a0001c0001t0001g0146 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.390+26661dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030810 | |||||
chrX:110030810 | CA | C | 91 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0066others(88): Show | 91 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.390+26661delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110030810 | |||||
chrX:110031069 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.390+26905C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110031069 | ||||||
chrX:110031374 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+27210C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110031374 | ||||||
chrX:110031516 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+27352T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110031516 | ||||||
chrX:110031523 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.390+27359A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110031523 | ||||||
chrX:110031620 | T | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+27456T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110031620 | ||||||
chrX:110031655 | G | GT | 4 | a0001c0001t0001g0177a0001c0001t0002g0081a0001c0001t0002g0154others(1): Show | 4 | HG00140.hp1 HG00735.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.390+27498dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110031655 | |||||
chrX:110031863 | T | TTTA | 5 | a0001c0001t0004g0007a0001c0001t0007g0006a0001c0001t0007g0019others(2): Show | 5 | HG01106.hp1 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+27716_390+2771 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110031863 | |||||
chrX:110031863 | T | TTTATTA | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+27713_390+2771 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110031863 | |||||
chrX:110032165 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.390+28001G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110032165 | ||||||
chrX:110032447 | G | GT | 2 | a0001c0001t0001g0146a0001c0001t0002g0121 | 2 | HG02155.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.390+28292dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110032447 | |||||
chrX:110032447 | G | T | 1 | a0001c0001t0003g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.390+28283G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110032447 | ||||||
chrX:110032480 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.390+28316T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110032480 | ||||||
chrX:110032516 | A | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+28352A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110032516 | ||||||
chrX:110033049 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.390+28885G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110033049 | ||||||
chrX:110033163 | G | A | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+28999G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110033163 | ||||||
chrX:110033283 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.390+29119C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110033283 | ||||||
chrX:110033955 | T | TC | 2 | a0001c0001t0001g0180a0001c0001t0028g0042 | 2 | HG02145.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.390+29798dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110033955 | |||||
chrX:110033964 | C | T | 1 | a0001c0001t0019g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.390+29800C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110033964 | ||||||
chrX:110034434 | T | G | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+30270T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110034434 | ||||||
chrX:110034498 | A | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+30334A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110034498 | ||||||
chrX:110034663 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+30499G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110034663 | ||||||
chrX:110034770 | C | T | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+30606C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110034770 | ||||||
chrX:110034844 | G | A | 193 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.390+30680G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110034844 | ||||||
chrX:110035081 | G | GA | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.390+30918dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035081 | |||||
chrX:110035237 | T | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+31073T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110035237 | ||||||
chrX:110035311 | TCTC | T | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.390+31150_390+3115 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035311 | |||||
chrX:110035388 | A | G | 1 | a0001c0001t0003g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+31224A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110035388 | ||||||
chrX:110035497 | C | T | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+31333C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110035497 | ||||||
chrX:110035504 | C | CT | 3 | a0001c0001t0001g0102a0001c0001t0013g0139a0001c0001t0024g0001 | 3 | HG02738.hp1 NA18906.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.390+31353dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035504 | |||||
chrX:110035504 | C | CTT | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.390+31352_390+3135 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035504 | |||||
chrX:110035747 | C | T | 2 | a0001c0001t0002g0125a0001c0001t0013g0139 | 2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.390+31583C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110035747 | ||||||
chrX:110035756 | C | T | 36 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.391-31591C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110035756 | ||||||
chrX:110035776 | A | AT | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-31558dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035776 | |||||
chrX:110035776 | AT | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.391-31558delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110035776 | |||||
chrX:110036061 | TA | T | 1 | a0001c0001t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.391-31279delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110036061 | |||||
chrX:110036270 | T | C | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-31077T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110036270 | ||||||
chrX:110036326 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391-31021T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110036326 | ||||||
chrX:110037241 | C | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(1): Show | 4 | HG01106.hp1 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-30106C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110037241 | ||||||
chrX:110037342 | G | A | 2 | a0001c0001t0002g0071a0001c0001t0003g0065 | 2 | HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.391-30005G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110037342 | ||||||
chrX:110037626 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.391-29721G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110037626 | ||||||
chrX:110037866 | C | T | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.391-29481C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110037866 | ||||||
chrX:110037984 | A | AT | 24 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0120others(21): Show | 24 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.391-29339dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | A | ATT | 2 | a0001c0001t0004g0095a0001c0001t0023g0096 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.391-29340_391-2933 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.391-29348_391-2933 others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.391-29349_391-2933 others(15): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.391-29350_391-2933 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | AT | A | 5 | a0001c0001t0001g0183a0001c0001t0002g0015a0001c0001t0004g0016others(2): Show | 5 | HG01884.hp1 HG02630.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-29339delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110037984 | ATT | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-29340_391-2933 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110037984 | |||||
chrX:110038021 | C | T | 1 | a0001c0001t0011g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391-29326C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038021 | ||||||
chrX:110038051 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.391-29296C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038051 | ||||||
chrX:110038178 | GA | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-29167delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110038178 | |||||
chrX:110038237 | C | T | 1 | a0001c0001t0008g0078 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.391-29110C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038237 | ||||||
chrX:110038238 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.391-29109G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038238 | ||||||
chrX:110038695 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-28652C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038695 | ||||||
chrX:110038714 | T | C | 3 | a0001c0001t0002g0085a0001c0001t0002g0162a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.391-28633T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038714 | ||||||
chrX:110038873 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.391-28474T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110038873 | ||||||
chrX:110039126 | T | G | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-28221T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110039126 | ||||||
chrX:110039290 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.391-28057G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110039290 | ||||||
chrX:110039341 | G | C | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-28006G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110039341 | ||||||
chrX:110039945 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-27402G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110039945 | ||||||
chrX:110040320 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-27027G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110040320 | ||||||
chrX:110040887 | G | A | 1 | a0001c0001t0014g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.391-26460G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110040887 | ||||||
chrX:110041095 | A | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-26252A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041095 | ||||||
chrX:110041172 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.391-26175T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041172 | ||||||
chrX:110041254 | C | A | 89 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.391-26093C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041254 | ||||||
chrX:110041259 | A | G | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.391-26088A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041259 | ||||||
chrX:110041278 | G | A | 1 | a0001c0001t0011g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391-26069G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041278 | ||||||
chrX:110041415 | G | A | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.391-25932G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041415 | ||||||
chrX:110041857 | A | T | 5 | a0001c0001t0002g0071a0001c0001t0002g0075a0001c0001t0002g0098others(2): Show | 5 | HG01258.hp1 HG01515.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-25490A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110041857 | ||||||
chrX:110042094 | T | C | 98 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.391-25253T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110042094 | ||||||
chrX:110042124 | C | G | 1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.391-25223C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110042124 | ||||||
chrX:110042130 | C | CT | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0109others(1): Show | 4 | NA18971.hp1 NA18988.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-25203dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110042130 | |||||
chrX:110042130 | CT | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-25203delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110042130 | |||||
chrX:110042621 | G | T | 3 | a0001c0001t0002g0015a0001c0001t0004g0016a0001c0001t0014g0047 | 3 | HG01884.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.391-24726G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110042621 | ||||||
chrX:110043142 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.391-24205G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110043142 | ||||||
chrX:110043673 | CA | C | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-23667delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110043673 | |||||
chrX:110043824 | T | A | 2 | a0001c0001t0002g0063a0001c0001t0004g0007 | 2 | HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.391-23523T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110043824 | ||||||
chrX:110043986 | T | C | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.391-23361T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110043986 | ||||||
chrX:110044080 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.391-23267G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110044080 | ||||||
chrX:110044425 | G | GT | 3 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0181 | 3 | HG01952.hp1 HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.391-22912dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110044425 | |||||
chrX:110044593 | C | CTTT | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-22727_391-2272 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110044593 | |||||
chrX:110044593 | CT | C | 127 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0058others(124): Show | 127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.391-22725delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110044593 | |||||
chrX:110044593 | CTT | C | 45 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0115others(42): Show | 45 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.391-22726_391-2272 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110044593 | |||||
chrX:110044593 | CTTT | C | 12 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0003g0043others(9): Show | 12 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-22727_391-2272 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110044593 | |||||
chrX:110044622 | T | C | 8 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0164others(5): Show | 8 | HG02015.hp1 HG02040.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-22725T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110044622 | ||||||
chrX:110045364 | A | G | 4 | a0001c0001t0004g0051a0001c0001t0004g0094a0001c0001t0004g0095others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-21983A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110045364 | ||||||
chrX:110046105 | A | G | 2 | a0001c0001t0003g0036a0001c0001t0003g0046 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.391-21242A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046105 | ||||||
chrX:110046138 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.391-21209G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046138 | ||||||
chrX:110046326 | G | A | 1 | a0001c0001t0015g0196 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.391-21021G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046326 | ||||||
chrX:110046435 | T | C | 8 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-20912T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046435 | ||||||
chrX:110046728 | C | A | 1 | a0001c0001t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.391-20619C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046728 | ||||||
chrX:110046840 | G | T | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.391-20507G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110046840 | ||||||
chrX:110047003 | A | T | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.391-20344A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110047003 | ||||||
chrX:110047134 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.391-20213A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110047134 | ||||||
chrX:110047136 | C | A | 1 | a0001c0001t0003g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.391-20211C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110047136 | ||||||
chrX:110047403 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.391-19944C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110047403 | ||||||
chrX:110047864 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.391-19483C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110047864 | ||||||
chrX:110048090 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.391-19257G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048090 | ||||||
chrX:110048092 | ACTCTATA others(51): Show |
A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391-19192_391-1913 others(62): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110048092 | |||||
chrX:110048138 | G | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391-19209G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048138 | ||||||
chrX:110048148 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.391-19199A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048148 | ||||||
chrX:110048240 | T | C | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.391-19107T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048240 | ||||||
chrX:110048431 | C | G | 1 | a0001c0001t0008g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.391-18916C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048431 | ||||||
chrX:110048486 | G | A | 3 | a0001c0001t0007g0019a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.391-18861G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048486 | ||||||
chrX:110048560 | G | GT | 2 | a0001c0001t0007g0019a0001c0001t0023g0096 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.391-18774dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110048560 | |||||
chrX:110048560 | GT | G | 1 | a0001c0001t0028g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.391-18774delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110048560 | |||||
chrX:110048573 | T | C | 1 | a0001c0001t0013g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391-18774T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048573 | ||||||
chrX:110048726 | T | C | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.391-18621T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048726 | ||||||
chrX:110048960 | A | G | 44 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.391-18387A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110048960 | ||||||
chrX:110049555 | C | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391-17792C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110049555 | ||||||
chrX:110049575 | T | C | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.391-17772T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110049575 | ||||||
chrX:110049580 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.391-17767G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110049580 | ||||||
chrX:110049581 | C | A | 1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.391-17766C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110049581 | ||||||
chrX:110049814 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-17533C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110049814 | ||||||
chrX:110050455 | C | A | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.391-16892C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110050455 | ||||||
chrX:110050543 | CTG | C | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-16801_391-1680 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110050543 | |||||
chrX:110050709 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.391-16638A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110050709 | ||||||
chrX:110051054 | CCTAT | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.391-16290_391-1628 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051054 | |||||
chrX:110051379 | G | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-15968G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110051379 | ||||||
chrX:110051583 | CA | C | 4 | a0001c0001t0001g0114a0001c0001t0002g0103a0001c0001t0002g0162others(1): Show | 4 | HG00738.hp1 HG01167.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-15751delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051583 | |||||
chrX:110051593 | A | AAAAAGAA others(2): Show |
1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-15751_391-1575 others(13): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051593 | |||||
chrX:110051593 | A | AAAAG | 44 | a0001c0001t0001g0115a0001c0001t0002g0041a0001c0001t0002g0063others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.391-15726_391-1572 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051593 | |||||
chrX:110051593 | A | AAAAGAAA others(1): Show |
1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.391-15730_391-1572 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051593 | |||||
chrX:110051593 | A | AAAG | 1 | a0001c0001t0003g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.391-15752_391-1575 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051593 | |||||
chrX:110051593 | AAAAG | A | 1 | a0001c0001t0002g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.391-15726_391-1572 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110051593 | |||||
chrX:110051876 | A | G | 2 | a0001c0001t0010g0010a0001c0001t0011g0009 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-15471A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110051876 | ||||||
chrX:110052224 | T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.391-15123T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110052224 | ||||||
chrX:110052604 | G | T | 44 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.391-14743G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110052604 | ||||||
chrX:110052745 | G | GT | 53 | a0001c0001t0001g0102a0001c0001t0001g0131a0001c0001t0001g0132others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.391-14579dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110052745 | |||||
chrX:110052745 | G | GTT | 4 | a0001c0001t0002g0136a0001c0001t0008g0077a0001c0001t0011g0026others(1): Show | 4 | HG01978.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-14580_391-1457 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110052745 | |||||
chrX:110052745 | GT | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0128 | 2 | HG02129.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.391-14579delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110052745 | |||||
chrX:110052876 | G | T | 1 | a0001c0001t0002g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.391-14471G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110052876 | ||||||
chrX:110052942 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.391-14405G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110052942 | ||||||
chrX:110052987 | A | G | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391-14360A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110052987 | ||||||
chrX:110053468 | T | C | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-13879T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110053468 | ||||||
chrX:110053504 | TAA | T | 1 | a0001c0001t0005g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.391-13838_391-1383 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110053504 | |||||
chrX:110053535 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.391-13812C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110053535 | ||||||
chrX:110054128 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.391-13219C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110054128 | ||||||
chrX:110054440 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.391-12907A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110054440 | ||||||
chrX:110054446 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.391-12901G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110054446 | ||||||
chrX:110054664 | A | G | 48 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(45): Show | 48 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.391-12683A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110054664 | ||||||
chrX:110054772 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.391-12575C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110054772 | ||||||
chrX:110055057 | G | T | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-12290G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110055057 | ||||||
chrX:110055116 | A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0171 | 2 | HG01928.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.391-12231A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110055116 | ||||||
chrX:110055186 | G | A | 47 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(44): Show | 47 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.391-12161G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110055186 | ||||||
chrX:110055330 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-12017C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110055330 | ||||||
chrX:110055761 | C | T | 2 | a0001c0001t0010g0010a0001c0001t0011g0009 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-11586C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110055761 | ||||||
chrX:110056002 | G | GT | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391-11339dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110056002 | |||||
chrX:110056102 | A | G | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.391-11245A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110056102 | ||||||
chrX:110056186 | C | T | 13 | a0001c0001t0003g0027a0001c0001t0003g0036a0001c0001t0003g0043others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.391-11161C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110056186 | ||||||
chrX:110056867 | A | G | 48 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(45): Show | 48 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.391-10480A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110056867 | ||||||
chrX:110056941 | T | TTA | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.391-10394_391-1039 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110056941 | |||||
chrX:110057020 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.391-10327G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110057020 | ||||||
chrX:110057448 | C | T | 196 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.391-9899C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110057448 | ||||||
chrX:110057532 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-9815G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110057532 | ||||||
chrX:110057548 | C | CT | 5 | a0001c0001t0002g0112a0001c0001t0003g0113a0001c0001t0004g0051others(2): Show | 5 | HG01106.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-9780dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110057548 | |||||
chrX:110057548 | C | CTT | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-9781_391-9780d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110057548 | |||||
chrX:110057548 | CT | C | 11 | a0001c0001t0001g0122a0001c0001t0001g0158a0001c0001t0001g0166others(8): Show | 11 | HG00408.hp2 HG00735.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.391-9780delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110057548 | |||||
chrX:110057950 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-9397C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110057950 | ||||||
chrX:110057988 | A | G | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.391-9359A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110057988 | ||||||
chrX:110058218 | T | C | 1 | a0001c0001t0002g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.391-9129T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110058218 | ||||||
chrX:110058344 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.391-9003T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110058344 | ||||||
chrX:110058609 | C | CT | 13 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0004g0003others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.391-8724dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110058609 | |||||
chrX:110058609 | C | CTT | 34 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.391-8725_391-8724d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110058609 | |||||
chrX:110058609 | C | CTTT | 3 | a0001c0001t0002g0070a0001c0001t0002g0093a0001c0001t0013g0139 | 3 | HG02293.hp2 HG02738.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.391-8726_391-8724d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110058609 | |||||
chrX:110058789 | A | AT | 1 | a0001c0001t0013g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.391-8544dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110058789 | |||||
chrX:110058789 | AT | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-8544delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110058789 | |||||
chrX:110058935 | A | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-8412A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110058935 | ||||||
chrX:110059193 | T | G | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-8154T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110059193 | ||||||
chrX:110059528 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.391-7819C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110059528 | ||||||
chrX:110059792 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-7555G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110059792 | ||||||
chrX:110059841 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-7506C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110059841 | ||||||
chrX:110060266 | G | GA | 4 | a0001c0001t0001g0177a0001c0001t0010g0010a0001c0001t0010g0091others(1): Show | 4 | HG02109.hp2 HG03486.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-7063dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110060266 | |||||
chrX:110060266 | G | GAA | 3 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0008g0078 | 3 | HG02451.hp2 HG03098.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.391-7064_391-7063d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110060266 | |||||
chrX:110060266 | G | GAAA | 39 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.391-7065_391-7063d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110060266 | |||||
chrX:110060266 | GA | G | 4 | a0001c0001t0001g0181a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-7063delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110060266 | |||||
chrX:110060281 | A | AAAG | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.391-7064_391-7063i others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110060281 | |||||
chrX:110060584 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-6763A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110060584 | ||||||
chrX:110060613 | T | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-6734T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110060613 | ||||||
chrX:110060752 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.391-6595A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110060752 | ||||||
chrX:110060821 | T | A | 2 | a0001c0001t0004g0051a0001c0001t0021g0017 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.391-6526T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110060821 | ||||||
chrX:110061180 | A | G | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-6167A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061180 | ||||||
chrX:110061299 | G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.391-6048G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061299 | ||||||
chrX:110061368 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-5979C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061368 | ||||||
chrX:110061412 | CT | C | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.391-5932delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110061412 | |||||
chrX:110061655 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.391-5692C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061655 | ||||||
chrX:110061781 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.391-5566G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061781 | ||||||
chrX:110061814 | G | T | 2 | a0001c0001t0003g0089a0001c0001t0012g0090 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.391-5533G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110061814 | ||||||
chrX:110062327 | A | G | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.391-5020A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110062327 | ||||||
chrX:110062356 | T | TTG | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.391-4975_391-4974d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110062356 | |||||
chrX:110062627 | A | AG | 3 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0005g0143 | 3 | HG01934.hp1 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.391-4718dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110062627 | |||||
chrX:110062726 | G | A | 1 | a0001c0001t0019g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.391-4621G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110062726 | ||||||
chrX:110062771 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.391-4576G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110062771 | ||||||
chrX:110062858 | A | G | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.391-4489A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110062858 | ||||||
chrX:110063530 | G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0146others(1): Show | 4 | HG02027.hp1 NA18940.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-3817G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110063530 | ||||||
chrX:110063542 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.391-3805A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110063542 | ||||||
chrX:110064994 | C | CA | 8 | a0001c0001t0003g0089a0001c0001t0004g0034a0001c0001t0009g0031others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-2328dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110064994 | CA | C | 98 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(95): Show | 98 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.391-2328delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110064994 | CAA | C | 8 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0114others(5): Show | 8 | HG01256.hp1 HG03209.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-2329_391-2328d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110064994 | CAAA | C | 4 | a0001c0001t0002g0041a0001c0001t0002g0093a0001c0001t0004g0003others(1): Show | 4 | HG02293.hp2 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-2330_391-2328d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110064994 | CAAAA | C | 34 | a0001c0001t0002g0063a0001c0001t0002g0068a0001c0001t0002g0069others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.391-2331_391-2328d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110064994 | CAAAAA | C | 4 | a0001c0001t0002g0074a0001c0001t0002g0125a0001c0001t0002g0184others(1): Show | 4 | HG01074.hp1 HG01168.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-2332_391-2328d others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110064994 | |||||
chrX:110065155 | A | G | 48 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(45): Show | 48 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.391-2192A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065155 | ||||||
chrX:110065225 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.391-2122T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065225 | ||||||
chrX:110065813 | CAT | C | 1 | a0001c0001t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.391-1531_391-1530d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110065813 | |||||
chrX:110065851 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.391-1496A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065851 | ||||||
chrX:110065857 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.391-1490A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065857 | ||||||
chrX:110065886 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.391-1461C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065886 | ||||||
chrX:110065898 | C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0001g0189others(1): Show | 4 | HG02602.hp1 HG03239.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-1449C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110065898 | ||||||
chrX:110066612 | A | G | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391-735A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110066612 | ||||||
chrX:110066632 | G | C | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391-715G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110066632 | ||||||
chrX:110066788 | G | A | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.391-559G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110066788 | ||||||
chrX:110066865 | A | C | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.391-482A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110066865 | ||||||
chrX:110066948 | G | C | 12 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0162others(9): Show | 12 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.391-399G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110066948 | ||||||
chrX:110067131 | CCTTCTCC others(4): Show |
C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.391-213_391-203del others(11): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067131 | |||||
chrX:110067151 | T | TGC | 2 | a0001c0001t0010g0010a0001c0001t0011g0009 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.391-193_391-192dup others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067151 | |||||
chrX:110067154 | G | GCA | 42 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0103others(39): Show | 42 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.391-169_391-168dup others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067154 | G | GCACA | 10 | a0001c0001t0002g0015a0001c0001t0003g0036a0001c0001t0003g0048others(7): Show | 10 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.391-171_391-168dup others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067154 | G | GCACACA | 2 | a0001c0001t0007g0014a0001c0001t0010g0091 | 2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.391-173_391-168dup others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067154 | G | GCGCA | 40 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(37): Show | 40 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-192_391-191ins others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067154 | G | GCGCACA | 2 | a0001c0001t0002g0112a0001c0001t0003g0113 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.391-192_391-191ins others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067154 | GCA | G | 2 | a0001c0001t0001g0189a0001c0001t0004g0007 | 2 | HG03098.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.391-169_391-168del others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 110067154 | |||||
chrX:110067156 | A | G | 1 | a0001c0001t0022g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.391-191A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110067156 | ||||||
chrX:110067203 | CAT | C | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391-143_391-142del others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110067203 | ||||||
chrX:110067278 | A | C | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.391-69A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 2/6 | chrX | 110067278 | ||||||
chrX:110067436 | T | C | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+40T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110067436 | ||||||
chrX:110067593 | G | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.440+197G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110067593 | ||||||
chrX:110068185 | G | C | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.440+789G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110068185 | ||||||
chrX:110068407 | A | C | 3 | a0001c0001t0002g0015a0001c0001t0004g0016a0001c0001t0014g0047 | 3 | HG01884.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.440+1011A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110068407 | ||||||
chrX:110069244 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.440+1848T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069244 | ||||||
chrX:110069248 | A | T | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.440+1852A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069248 | ||||||
chrX:110069326 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.440+1930G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069326 | ||||||
chrX:110069545 | C | T | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.440+2149C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069545 | ||||||
chrX:110069570 | C | CT | 2 | a0001c0001t0001g0164a0001c0001t0003g0018 | 2 | NA18906.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.440+2190dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110069570 | |||||
chrX:110069570 | C | CTTT | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+2188_440+2190d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110069570 | |||||
chrX:110069570 | CT | C | 54 | a0001c0001t0001g0039a0001c0001t0001g0097a0001c0001t0002g0041others(51): Show | 54 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.440+2190delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110069570 | |||||
chrX:110069570 | CTT | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+2189_440+2190d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110069570 | |||||
chrX:110069586 | T | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0174 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.440+2190T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069586 | ||||||
chrX:110069631 | C | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+2235C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069631 | ||||||
chrX:110069799 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+2403G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110069799 | ||||||
chrX:110070107 | G | A | 45 | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(42): Show | 45 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+2711G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110070107 | ||||||
chrX:110070142 | C | T | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.440+2746C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110070142 | ||||||
chrX:110070512 | G | A | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+3116G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110070512 | ||||||
chrX:110070714 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.440+3318G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110070714 | ||||||
chrX:110071151 | A | ATATT | 40 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(37): Show | 40 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.440+3790_440+3793d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071151 | |||||
chrX:110071151 | A | ATATTTAT others(1): Show |
1 | a0001c0001t0026g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.440+3786_440+3793d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071151 | |||||
chrX:110071151 | ATATT | A | 107 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(104): Show | 107 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.440+3790_440+3793d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071151 | |||||
chrX:110071151 | ATATTTAT others(1): Show |
A | 3 | a0001c0001t0002g0116a0001c0001t0002g0136a0001c0001t0013g0135 | 3 | HG00408.hp2 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.440+3786_440+3793d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071151 | |||||
chrX:110071255 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+3859G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110071255 | ||||||
chrX:110071677 | C | A | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.440+4281C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110071677 | ||||||
chrX:110071716 | C | CA | 14 | a0001c0001t0001g0133a0001c0001t0001g0178a0001c0001t0002g0075others(11): Show | 14 | HG00609.hp1 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.440+4343dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | C | CAA | 33 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(30): Show | 33 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.440+4342_440+4343d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | C | CAAA | 4 | a0001c0001t0002g0072a0001c0001t0002g0081a0001c0001t0002g0134others(1): Show | 4 | HG00735.hp2 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+4341_440+4343d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | C | CAAAA | 1 | a0001c0001t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.440+4340_440+4343d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | C | CAAAAA | 1 | a0001c0001t0002g0110 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.440+4339_440+4343d others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | CA | C | 4 | a0001c0001t0001g0122a0001c0001t0004g0007a0001c0001t0005g0092others(1): Show | 4 | HG01496.hp1 HG03098.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+4343delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | CAAAAAAA | C | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.440+4337_440+4343d others(9): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110071716 | CAAAAAAA others(1): Show |
C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.440+4336_440+4343d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110071716 | |||||
chrX:110072088 | G | A | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+4692G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072088 | ||||||
chrX:110072093 | G | A | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+4697G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072093 | ||||||
chrX:110072118 | T | A | 43 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.440+4722T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072118 | ||||||
chrX:110072296 | C | CA | 21 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0001g0188others(18): Show | 21 | HG01884.hp1 HG02074.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.440+4921dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110072296 | |||||
chrX:110072296 | C | CAA | 2 | a0001c0001t0003g0046a0001c0001t0028g0042 | 2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.440+4920_440+4921d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110072296 | |||||
chrX:110072296 | CA | C | 46 | a0001c0001t0001g0156a0001c0001t0001g0192a0001c0001t0002g0041others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.440+4921delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110072296 | |||||
chrX:110072296 | CAA | C | 1 | a0001c0001t0002g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.440+4920_440+4921d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110072296 | |||||
chrX:110072593 | T | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.440+5197T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072593 | ||||||
chrX:110072658 | T | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.440+5262T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072658 | ||||||
chrX:110072793 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.440+5397A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072793 | ||||||
chrX:110072838 | T | C | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.440+5442T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072838 | ||||||
chrX:110072839 | T | C | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.440+5443T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110072839 | ||||||
chrX:110073348 | C | A | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.440+5952C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073348 | ||||||
chrX:110073737 | C | A | 1 | a0001c0001t0004g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440+6341C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073737 | ||||||
chrX:110073874 | T | TTTG | 1 | a0001c0001t0001g0176 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.440+6493_440+6495d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110073874 | |||||
chrX:110073908 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.440+6512C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073908 | ||||||
chrX:110073967 | T | C | 150 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(147): Show | 150 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.440+6571T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073967 | ||||||
chrX:110073971 | G | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.440+6575G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073971 | ||||||
chrX:110073971 | G | T | 149 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(146): Show | 149 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.440+6575G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110073971 | ||||||
chrX:110074208 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.440+6812A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110074208 | ||||||
chrX:110074211 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.440+6815G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110074211 | ||||||
chrX:110074373 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+6977G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110074373 | ||||||
chrX:110074891 | C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0159others(1): Show | 4 | HG02074.hp1 HG02132.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+7495C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110074891 | ||||||
chrX:110074892 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.440+7496G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110074892 | ||||||
chrX:110075636 | A | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+8240A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110075636 | ||||||
chrX:110075679 | T | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+8283T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110075679 | ||||||
chrX:110075886 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.440+8490T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110075886 | ||||||
chrX:110075995 | TCTC | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG02027.hp1 NA18940.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.440+8605_440+8607d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110075995 | |||||
chrX:110076006 | AT | A | 10 | a0001c0001t0001g0166a0001c0001t0001g0173a0001c0001t0001g0181others(7): Show | 10 | HG01891.hp1 HG01978.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.440+8629delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110076006 | |||||
chrX:110076006 | ATT | A | 181 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(178): Show | 181 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.440+8628_440+8629d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110076006 | |||||
chrX:110076006 | ATTT | A | 5 | a0001c0001t0001g0117a0001c0001t0002g0071a0001c0001t0003g0022others(2): Show | 5 | HG01981.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+8627_440+8629d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110076006 | |||||
chrX:110076010 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.440+8614T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076010 | ||||||
chrX:110076096 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+8700G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076096 | ||||||
chrX:110076125 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+8729T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076125 | ||||||
chrX:110076271 | T | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.440+8875T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076271 | ||||||
chrX:110076499 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.440+9103T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076499 | ||||||
chrX:110076637 | GC | G | 1 | a0001c0001t0003g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.440+9242delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110076637 | ||||||
chrX:110077030 | G | T | 38 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.440+9634G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110077030 | ||||||
chrX:110077409 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+10013A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110077409 | ||||||
chrX:110077706 | T | C | 5 | a0001c0001t0004g0045a0001c0001t0004g0054a0001c0001t0004g0094others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+10310T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110077706 | ||||||
chrX:110077776 | A | G | 2 | a0001c0001t0004g0051a0001c0001t0021g0017 | 2 | HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.440+10380A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110077776 | ||||||
chrX:110077926 | A | G | 48 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(45): Show | 48 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.440+10530A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110077926 | ||||||
chrX:110078140 | A | G | 1 | a0001c0001t0013g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.440+10744A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078140 | ||||||
chrX:110078163 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+10767C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078163 | ||||||
chrX:110078169 | T | TA | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+10773_440+1077 others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078169 | ||||||
chrX:110078446 | A | G | 1 | a0001c0001t0012g0153 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.440+11050A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078446 | ||||||
chrX:110078705 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.440+11309G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078705 | ||||||
chrX:110078861 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.440+11465A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110078861 | ||||||
chrX:110079168 | C | T | 45 | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(42): Show | 45 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+11772C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110079168 | ||||||
chrX:110079552 | T | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.440+12156T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110079552 | ||||||
chrX:110079842 | A | AG | 1 | a0001c0001t0002g0110 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.440+12452dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110079842 | |||||
chrX:110079987 | T | TA | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+12599dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110079987 | |||||
chrX:110080233 | G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0018 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.440+12837G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110080233 | ||||||
chrX:110080261 | A | G | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.440+12865A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110080261 | ||||||
chrX:110080356 | G | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.440+12960G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110080356 | ||||||
chrX:110080463 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+13067G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110080463 | ||||||
chrX:110080566 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.440+13170G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110080566 | ||||||
chrX:110080888 | A | AT | 29 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0102others(26): Show | 29 | HG00735.hp1 HG01261.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.440+13520dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110080888 | AT | A | 44 | a0001c0001t0001g0073a0001c0001t0001g0189a0001c0001t0002g0015others(41): Show | 44 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.440+13520delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110080888 | ATT | A | 3 | a0001c0001t0003g0004a0001c0001t0003g0048a0001c0001t0027g0084 | 3 | HG02717.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.440+13519_440+1352 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110080888 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0143 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.440+13511_440+1352 others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110080888 | ATTTTTTT others(4): Show |
A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.440+13510_440+1352 others(15): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110080888 | ATTTTTTT others(6): Show |
A | 41 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(38): Show | 41 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.440+13508_440+1352 others(17): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110080888 | |||||
chrX:110081379 | A | G | 44 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.440+13983A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110081379 | ||||||
chrX:110081640 | A | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0116a0001c0001t0002g0136others(2): Show | 5 | HG00408.hp2 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.440+14244A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110081640 | ||||||
chrX:110081826 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+14430C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110081826 | ||||||
chrX:110081923 | G | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+14527G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110081923 | ||||||
chrX:110082206 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.440+14810C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110082206 | ||||||
chrX:110082258 | T | C | 44 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.440+14862T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110082258 | ||||||
chrX:110082464 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.440+15068G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110082464 | ||||||
chrX:110082598 | G | T | 47 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(44): Show | 47 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.440+15202G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110082598 | ||||||
chrX:110082729 | C | T | 4 | a0001c0001t0002g0071a0001c0001t0002g0098a0001c0001t0003g0065others(1): Show | 4 | HG01258.hp1 HG01515.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+15333C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110082729 | ||||||
chrX:110083744 | A | G | 2 | a0001c0001t0007g0006a0001c0001t0010g0091 | 2 | HG01106.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.440+16348A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110083744 | ||||||
chrX:110083930 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+16534G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110083930 | ||||||
chrX:110084349 | C | CTATACTA others(62): Show |
1 | a0001c0001t0002g0069 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.440+16957_440+1695 others(73): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(80): Show |
1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.440+16965_440+1696 others(91): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(49): Show |
46 | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(43): Show | 46 | HG01099.hp1 HG01106.hp1 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.440+16965_440+1696 others(60): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(80): Show |
80 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0058others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.440+16965_440+1696 others(91): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(109): Show |
1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.440+16965_440+1696 others(120): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(111): Show |
9 | a0001c0001t0001g0040a0001c0001t0001g0099a0001c0001t0001g0128others(6): Show | 9 | HG00621.hp1 HG02129.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.440+16965_440+1696 others(122): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(111): Show |
1 | a0001c0001t0023g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.440+16965_440+1696 others(122): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(142): Show |
4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0133others(1): Show | 4 | HG02135.hp1 NA18944.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+16965_440+1696 others(153): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(84): Show |
2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.440+16965_440+1696 others(95): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(50): Show |
1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.440+16965_440+1696 others(61): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(61): Show |
42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+16965_440+1696 others(72): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(62): Show |
2 | a0001c0001t0002g0075a0001c0001t0027g0084 | 2 | HG02717.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.440+16965_440+1696 others(73): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(61): Show |
1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+16965_440+1696 others(72): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084349 | C | CTATATAT others(84): Show |
1 | a0001c0001t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.440+16965_440+1696 others(95): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084349 | |||||
chrX:110084351 | A | ATATATAT others(80): Show |
3 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0028 | 3 | HG02257.hp2 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.440+16965_440+1696 others(91): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084351 | |||||
chrX:110084362 | G | C | 2 | a0001c0001t0005g0092a0001c0001t0010g0091 | 2 | NA19005.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.440+16966G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084362 | ||||||
chrX:110084365 | T | TACTATAT others(30): Show |
1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+16970_440+1697 others(41): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084365 | |||||
chrX:110084366 | A | ACTATATA others(64): Show |
1 | a0001c0001t0005g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.440+16970_440+1697 others(75): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084366 | ||||||
chrX:110084367 | G | A | 1 | a0001c0001t0005g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.440+16971G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084367 | ||||||
chrX:110084367 | G | GTA | 17 | a0001c0001t0001g0040a0001c0001t0001g0099a0001c0001t0001g0128others(14): Show | 17 | HG00621.hp1 HG01891.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.440+16980_440+1698 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084367 | |||||
chrX:110084377 | AGT | A | 1 | a0001c0001t0002g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.440+16984_440+1698 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084377 | |||||
chrX:110084378 | G | T | 90 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.440+16982G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084378 | ||||||
chrX:110084379 | T | A | 45 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(42): Show | 45 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+16983T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084379 | ||||||
chrX:110084379 | T | AGTATATA others(24): Show |
45 | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(42): Show | 45 | HG01099.hp1 HG01106.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+16982_440+1698 others(35): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084379 | ||||||
chrX:110084380 | G | A | 4 | a0001c0001t0005g0092a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+16984G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084380 | ||||||
chrX:110084380 | G | GTATATAT others(26): Show |
2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.440+17016_440+1701 others(37): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084380 | |||||
chrX:110084382 | A | AG | 1 | a0001c0001t0005g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.440+16986_440+1698 others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084382 | ||||||
chrX:110084382 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.440+16986A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084382 | ||||||
chrX:110084398 | GTA | G | 2 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.440+17013_440+1701 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084398 | |||||
chrX:110084400 | A | ATATATAT others(20): Show |
1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+17016_440+1701 others(31): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084400 | |||||
chrX:110084413 | G | A | 65 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0129others(62): Show | 65 | HG00621.hp1 HG00738.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.440+17017G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084413 | ||||||
chrX:110084413 | G | GTGTATAT others(26): Show |
1 | a0001c0001t0001g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.440+17018_440+1701 others(37): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084413 | |||||
chrX:110084431 | G | C | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.440+17035G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084431 | ||||||
chrX:110084433 | A | ATATATAT others(24): Show |
2 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.440+17048_440+1707 others(35): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084433 | |||||
chrX:110084446 | A | G | 3 | a0001c0001t0001g0161a0001c0001t0004g0007a0001c0001t0027g0084 | 3 | HG01928.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.440+17050A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084446 | ||||||
chrX:110084464 | G | GTA | 3 | a0001c0001t0003g0027a0001c0001t0007g0019a0001c0001t0017g0179 | 3 | HG02723.hp1 NA18989.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.440+17081_440+1708 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084464 | |||||
chrX:110084466 | A | ATATATAT others(24): Show |
1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+17080_440+1708 others(35): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084466 | |||||
chrX:110084477 | T | G | 3 | a0001c0001t0004g0007a0001c0001t0005g0175a0001c0001t0010g0010 | 3 | HG02109.hp2 HG03098.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.440+17081T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084477 | ||||||
chrX:110084477 | T | TAG | 1 | a0001c0001t0003g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.440+17103_440+1710 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084477 | |||||
chrX:110084477 | TAG | T | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+17103_440+1710 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110084477 | |||||
chrX:110084479 | G | T | 119 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0059others(116): Show | 119 | HG00609.hp1 HG00621.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.440+17083G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084479 | ||||||
chrX:110084481 | G | T | 27 | a0001c0001t0001g0128a0001c0001t0001g0152a0001c0001t0001g0166others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.440+17085G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084481 | ||||||
chrX:110084483 | G | T | 6 | a0001c0001t0001g0197a0001c0001t0002g0103a0001c0001t0002g0104others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+17087G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084483 | ||||||
chrX:110084868 | T | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0138a0001c0001t0001g0158others(2): Show | 5 | HG00609.hp1 HG01256.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+17472T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110084868 | ||||||
chrX:110085157 | C | CT | 2 | a0001c0001t0001g0197a0001c0001t0015g0196 | 2 | NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.440+17776dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110085157 | |||||
chrX:110085304 | G | A | 7 | a0001c0001t0003g0036a0001c0001t0003g0046a0001c0001t0003g0048others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+17908G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085304 | ||||||
chrX:110085329 | T | TA | 42 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.440+17941dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110085329 | |||||
chrX:110085329 | TA | T | 2 | a0001c0001t0002g0086a0001c0001t0004g0016 | 2 | HG01168.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.440+17941delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110085329 | |||||
chrX:110085335 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+17939A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085335 | ||||||
chrX:110085336 | A | AAT | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.440+17957_440+1795 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110085336 | |||||
chrX:110085336 | A | AT | 2 | a0001c0001t0002g0015a0001c0001t0014g0047 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.440+17940_440+1794 others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085336 | ||||||
chrX:110085336 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.440+17940A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085336 | ||||||
chrX:110085337 | AT | A | 55 | a0001c0001t0002g0085a0001c0001t0002g0103a0001c0001t0002g0104others(52): Show | 55 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.440+17942delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085337 | ||||||
chrX:110085338 | T | A | 6 | a0001c0001t0001g0130a0001c0001t0002g0110a0001c0001t0006g0106others(3): Show | 6 | HG02040.hp1 HG02135.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+17942T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085338 | ||||||
chrX:110085340 | T | A | 8 | a0001c0001t0001g0130a0001c0001t0004g0045a0001c0001t0004g0054others(5): Show | 8 | HG02055.hp1 HG02135.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.440+17944T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085340 | ||||||
chrX:110085822 | A | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+18426A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085822 | ||||||
chrX:110085890 | G | C | 7 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(4): Show | 7 | HG00621.hp1 HG02129.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.440+18494G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110085890 | ||||||
chrX:110086190 | T | C | 1 | a0001c0001t0022g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.440+18794T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110086190 | ||||||
chrX:110086584 | ATATATAT others(11): Show |
A | 196 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.440+19232_440+1924 others(22): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110086584 | |||||
chrX:110086674 | A | ATG | 45 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(42): Show | 45 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+19292_440+1929 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110086674 | |||||
chrX:110086688 | G | GTA | 49 | a0001c0001t0002g0015a0001c0001t0002g0085a0001c0001t0002g0086others(46): Show | 49 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.440+19301_440+1930 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110086688 | |||||
chrX:110086690 | A | G | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.440+19294A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110086690 | ||||||
chrX:110087286 | T | A | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.440+19890T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087286 | ||||||
chrX:110087359 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.440+19963C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087359 | ||||||
chrX:110087448 | C | A | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.440+20052C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087448 | ||||||
chrX:110087509 | T | C | 45 | a0001c0001t0002g0041a0001c0001t0002g0063a0001c0001t0002g0068others(42): Show | 45 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.440+20113T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087509 | ||||||
chrX:110087788 | G | C | 1 | a0001c0001t0005g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.440+20392G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087788 | ||||||
chrX:110087881 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.440+20485A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110087881 | ||||||
chrX:110088098 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.440+20702T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088098 | ||||||
chrX:110088252 | A | AC | 1 | a0001c0001t0001g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441-20823dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110088252 | |||||
chrX:110088357 | G | T | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441-20723G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088357 | ||||||
chrX:110088393 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-20687G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088393 | ||||||
chrX:110088418 | T | A | 1 | a0002c0002t0001g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.441-20662T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088418 | ||||||
chrX:110088666 | G | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-20414G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088666 | ||||||
chrX:110088684 | G | C | 13 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.441-20396G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088684 | ||||||
chrX:110088737 | A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0066 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.441-20343A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088737 | ||||||
chrX:110088907 | T | C | 13 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.441-20173T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110088907 | ||||||
chrX:110090114 | T | C | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.441-18966T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110090114 | ||||||
chrX:110090226 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.441-18854G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110090226 | ||||||
chrX:110090263 | C | CT | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.441-18806dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110090263 | |||||
chrX:110090311 | A | AT | 14 | a0001c0001t0003g0036a0001c0001t0003g0038a0001c0001t0003g0046others(11): Show | 14 | HG01106.hp1 HG01243.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.441-18756dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110090311 | |||||
chrX:110090311 | A | ATT | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-18757_441-1875 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110090311 | |||||
chrX:110090356 | A | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-18724A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110090356 | ||||||
chrX:110090859 | G | GC | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.441-18215dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110090859 | |||||
chrX:110091037 | T | C | 7 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-18043T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091037 | ||||||
chrX:110091425 | C | T | 8 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-17655C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091425 | ||||||
chrX:110091434 | T | C | 1 | a0001c0001t0018g0191 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.441-17646T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091434 | ||||||
chrX:110091457 | A | G | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441-17623A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091457 | ||||||
chrX:110091550 | G | A | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.441-17530G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091550 | ||||||
chrX:110091601 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.441-17479C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110091601 | ||||||
chrX:110092043 | G | C | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-17037G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092043 | ||||||
chrX:110092317 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-16763A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092317 | ||||||
chrX:110092383 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.441-16697A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092383 | ||||||
chrX:110092445 | G | C | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-16635G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092445 | ||||||
chrX:110092606 | G | T | 11 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-16474G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092606 | ||||||
chrX:110092838 | C | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.441-16242C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110092838 | ||||||
chrX:110093140 | A | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.441-15940A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093140 | ||||||
chrX:110093179 | G | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0052a0001c0001t0003g0055others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-15901G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093179 | ||||||
chrX:110093280 | G | A | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-15800G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093280 | ||||||
chrX:110093724 | C | T | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.441-15356C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093724 | ||||||
chrX:110093755 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-15325C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093755 | ||||||
chrX:110093884 | A | G | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.441-15196A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093884 | ||||||
chrX:110093944 | A | G | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.441-15136A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110093944 | ||||||
chrX:110094339 | A | G | 8 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-14741A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110094339 | ||||||
chrX:110094502 | A | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.441-14578A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110094502 | ||||||
chrX:110094540 | C | A | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441-14540C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110094540 | ||||||
chrX:110094693 | G | T | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.441-14387G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110094693 | ||||||
chrX:110094839 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-14241G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110094839 | ||||||
chrX:110095011 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-14069T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095011 | ||||||
chrX:110095038 | C | T | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441-14042C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095038 | ||||||
chrX:110095193 | T | C | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441-13887T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095193 | ||||||
chrX:110095297 | C | T | 18 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0162others(15): Show | 18 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.441-13783C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095297 | ||||||
chrX:110095709 | G | C | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.441-13371G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095709 | ||||||
chrX:110095848 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.441-13232C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095848 | ||||||
chrX:110095926 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-13154G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095926 | ||||||
chrX:110095989 | CTGCAGAA others(10): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.441-13078_441-1306 others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110095989 | |||||
chrX:110095990 | T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0066 | 2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.441-13090T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110095990 | ||||||
chrX:110096091 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.441-12989G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096091 | ||||||
chrX:110096481 | C | A | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.441-12599C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096481 | ||||||
chrX:110096517 | G | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441-12563G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096517 | ||||||
chrX:110096530 | A | T | 1 | a0001c0001t0002g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.441-12550A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096530 | ||||||
chrX:110096566 | A | G | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441-12514A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096566 | ||||||
chrX:110096634 | C | G | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-12446C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096634 | ||||||
chrX:110096636 | C | A | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.441-12444C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096636 | ||||||
chrX:110096949 | G | A | 13 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.441-12131G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110096949 | ||||||
chrX:110097089 | C | T | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.441-11991C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097089 | ||||||
chrX:110097117 | G | C | 1 | a0001c0001t0008g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441-11963G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097117 | ||||||
chrX:110097652 | T | G | 13 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(10): Show | 13 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.441-11428T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097652 | ||||||
chrX:110097785 | G | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441-11295G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097785 | ||||||
chrX:110097856 | G | A | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.441-11224G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097856 | ||||||
chrX:110097906 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.441-11174T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110097906 | ||||||
chrX:110098161 | G | A | 9 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(6): Show | 9 | HG01106.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.441-10919G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098161 | ||||||
chrX:110098444 | A | G | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441-10636A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098444 | ||||||
chrX:110098573 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.441-10507G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098573 | ||||||
chrX:110098587 | C | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441-10493C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098587 | ||||||
chrX:110098758 | G | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441-10322G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098758 | ||||||
chrX:110098795 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.441-10285T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098795 | ||||||
chrX:110098801 | C | CT | 3 | a0001c0001t0001g0144a0001c0001t0001g0180a0001c0001t0007g0006 | 3 | HG01106.hp1 HG01934.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.441-10266dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110098801 | |||||
chrX:110098801 | CT | C | 4 | a0001c0001t0001g0115a0001c0001t0002g0075a0001c0001t0008g0077others(1): Show | 4 | HG01884.hp2 HG03239.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-10266delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110098801 | |||||
chrX:110098909 | C | A | 100 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(97): Show | 100 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.441-10171C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110098909 | ||||||
chrX:110098950 | A | AT | 16 | a0001c0001t0001g0039a0001c0001t0001g0130a0001c0001t0001g0160others(13): Show | 16 | HG00280.hp1 HG00735.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.441-10109dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110098950 | |||||
chrX:110098950 | A | ATT | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441-10110_441-1010 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110098950 | |||||
chrX:110098950 | AT | A | 8 | a0001c0001t0004g0007a0001c0001t0007g0006a0001c0001t0007g0019others(5): Show | 8 | HG01106.hp1 HG02258.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-10109delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110098950 | |||||
chrX:110099020 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-10060G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110099020 | ||||||
chrX:110099284 | A | AT | 4 | a0001c0001t0001g0099a0001c0001t0001g0187a0001c0001t0001g0189others(1): Show | 4 | HG02602.hp1 HG03239.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-9786dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110099284 | |||||
chrX:110099602 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.441-9478G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110099602 | ||||||
chrX:110099955 | C | A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.441-9125C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110099955 | ||||||
chrX:110100229 | G | A | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441-8851G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100229 | ||||||
chrX:110100267 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441-8813C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100267 | ||||||
chrX:110100413 | A | G | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-8667A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100413 | ||||||
chrX:110100636 | A | G | 1 | a0001c0001t0008g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441-8444A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100636 | ||||||
chrX:110100716 | C | T | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-8364C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100716 | ||||||
chrX:110100746 | A | AT | 2 | a0001c0001t0001g0181a0001c0001t0004g0007 | 2 | HG01978.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.441-8324dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110100746 | |||||
chrX:110100817 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.441-8263C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100817 | ||||||
chrX:110100856 | T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.441-8224T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100856 | ||||||
chrX:110100894 | T | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0155 | 3 | HG01069.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.441-8186T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110100894 | ||||||
chrX:110101311 | A | G | 4 | a0001c0001t0002g0071a0001c0001t0002g0098a0001c0001t0003g0065others(1): Show | 4 | HG01258.hp1 HG01515.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-7769A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110101311 | ||||||
chrX:110101527 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441-7553G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110101527 | ||||||
chrX:110101579 | GA | G | 3 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0028 | 3 | HG02257.hp2 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.441-7500delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110101579 | ||||||
chrX:110101580 | A | AT | 8 | a0001c0001t0001g0105a0001c0001t0001g0168a0001c0001t0001g0180others(5): Show | 8 | HG00735.hp1 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-7483dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110101580 | |||||
chrX:110101580 | A | ATT | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0037others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.441-7484_441-7483d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110101580 | |||||
chrX:110101580 | A | ATTT | 2 | a0001c0001t0007g0006a0001c0001t0010g0035 | 2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.441-7485_441-7483d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110101580 | |||||
chrX:110101580 | AT | A | 2 | a0001c0001t0001g0040a0001c0001t0011g0026 | 2 | HG02258.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.441-7483delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110101580 | |||||
chrX:110101769 | G | C | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-7311G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110101769 | ||||||
chrX:110102010 | G | A | 1 | a0001c0001t0012g0153 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.441-7070G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110102010 | ||||||
chrX:110102085 | G | A | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441-6995G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110102085 | ||||||
chrX:110102171 | C | CA | 12 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0158others(9): Show | 12 | HG00621.hp1 HG01256.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.441-6895dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110102171 | |||||
chrX:110102171 | CA | C | 3 | a0001c0001t0001g0170a0001c0001t0002g0015a0001c0001t0014g0047 | 3 | HG01884.hp1 HG03579.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.441-6895delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110102171 | |||||
chrX:110102207 | A | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-6873A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110102207 | ||||||
chrX:110103102 | T | C | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441-5978T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110103102 | ||||||
chrX:110103265 | T | C | 8 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-5815T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110103265 | ||||||
chrX:110103474 | G | A | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-5606G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110103474 | ||||||
chrX:110103530 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441-5550G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110103530 | ||||||
chrX:110103559 | G | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-5521G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110103559 | ||||||
chrX:110104410 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441-4670C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110104410 | ||||||
chrX:110104554 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.441-4526T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110104554 | ||||||
chrX:110104681 | T | C | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-4399T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110104681 | ||||||
chrX:110104708 | TTC | T | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.441-4368_441-4367d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110104708 | |||||
chrX:110104718 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441-4362G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110104718 | ||||||
chrX:110105063 | C | T | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-4017C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105063 | ||||||
chrX:110105072 | A | AT | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.441-4000dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105072 | |||||
chrX:110105107 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.441-3973C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105107 | ||||||
chrX:110105175 | A | ACCAT | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.441-3863_441-3860d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105175 | |||||
chrX:110105175 | ACCAT | A | 98 | a0001c0001t0001g0115a0001c0001t0001g0166a0001c0001t0001g0193others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.441-3863_441-3860d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105175 | |||||
chrX:110105175 | ACCATCCA others(13): Show |
A | 2 | a0001c0001t0007g0006a0001c0001t0007g0019 | 2 | HG01106.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.441-3879_441-3860d others(22): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105175 | |||||
chrX:110105679 | G | GAC | 24 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0088others(21): Show | 24 | HG00642.hp1 HG00738.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.441-3361_441-3360d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | G | GACAC | 18 | a0001c0001t0001g0197a0001c0001t0002g0015a0001c0001t0003g0025others(15): Show | 18 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.441-3363_441-3360d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | G | GACACAC | 19 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0003g0004others(16): Show | 19 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-3365_441-3360d others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | G | GACACACA others(1): Show |
2 | a0001c0001t0002g0085a0001c0001t0004g0034 | 2 | NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.441-3367_441-3360d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | GAC | G | 20 | a0001c0001t0001g0040a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG00621.hp1 HG01071.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.441-3361_441-3360d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | GACAC | G | 4 | a0001c0001t0002g0041a0001c0001t0002g0056a0001c0001t0002g0072others(1): Show | 4 | HG01358.hp1 HG01433.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-3363_441-3360d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105679 | GACACACA others(11): Show |
G | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441-3377_441-3360d others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105679 | |||||
chrX:110105683 | C | CACAG | 1 | a0001c0001t0022g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441-3394_441-3393i others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105683 | |||||
chrX:110105684 | A | ACACAC | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.441-3395_441-3391d others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105684 | |||||
chrX:110105685 | C | CAG | 2 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441-3394_441-3393i others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105685 | |||||
chrX:110105691 | CACACACA others(23): Show |
C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.441-3377_441-3348d others(32): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105691 | |||||
chrX:110105705 | CACACACA others(31): Show |
C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-3373_441-3336d others(40): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105705 | |||||
chrX:110105733 | G | C | 2 | a0001c0001t0002g0162a0001c0001t0012g0153 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.441-3347G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105733 | ||||||
chrX:110105748 | AAT | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-3331_441-3330d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105748 | ||||||
chrX:110105750 | T | TAGA | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.441-3330_441-3329i others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105750 | ||||||
chrX:110105750 | T | TGA | 51 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0060others(48): Show | 51 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.441-3287_441-3286d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGA | 14 | a0001c0001t0001g0040a0001c0001t0001g0102a0001c0001t0001g0105others(11): Show | 14 | HG00609.hp1 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.441-3289_441-3286d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGA | 12 | a0001c0001t0001g0039a0001c0001t0001g0131a0001c0001t0001g0137others(9): Show | 12 | HG00280.hp1 HG00673.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.441-3291_441-3286d others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(1): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0010g0010 | 3 | HG00735.hp1 HG02109.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.441-3293_441-3286d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(3): Show |
3 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0172 | 3 | HG00621.hp1 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.441-3295_441-3286d others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(5): Show |
2 | a0001c0001t0001g0067a0001c0001t0005g0100 | 2 | HG02083.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.441-3297_441-3286d others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(7): Show |
2 | a0001c0001t0001g0128a0001c0001t0006g0150 | 2 | HG02129.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.441-3299_441-3286d others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(9): Show |
1 | a0001c0001t0006g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.441-3301_441-3286d others(18): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | T | TGAGAGAG others(11): Show |
1 | a0001c0001t0006g0140 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.441-3303_441-3286d others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | TGA | T | 18 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0192others(15): Show | 18 | HG01074.hp1 HG01169.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.441-3287_441-3286d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | TGAGA | T | 58 | a0001c0001t0002g0015a0001c0001t0002g0063a0001c0001t0002g0070others(55): Show | 58 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.441-3289_441-3286d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | TGAGAGA | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0145others(4): Show | 7 | HG00735.hp2 HG01106.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-3291_441-3286d others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | TGAGAGAG others(1): Show |
T | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-3293_441-3286d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105750 | TGAGAGAG others(3): Show |
T | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-3295_441-3286d others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105750 | |||||
chrX:110105751 | GAGA | G | 1 | a0002c0002t0001g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.441-3328_441-3326d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105751 | ||||||
chrX:110105763 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-3317G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105763 | ||||||
chrX:110105764 | A | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-3316A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105764 | ||||||
chrX:110105791 | GAGA | G | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.441-3287_441-3285d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105791 | |||||
chrX:110105792 | A | AGG | 1 | a0001c0001t0005g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.441-3287_441-3286i others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110105792 | |||||
chrX:110105851 | T | G | 8 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(5): Show | 8 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.441-3229T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110105851 | ||||||
chrX:110106373 | C | CT | 19 | a0001c0001t0001g0040a0001c0001t0001g0088a0001c0001t0001g0105others(16): Show | 19 | HG00673.hp1 HG01106.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.441-2689dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110106373 | |||||
chrX:110106373 | C | CTT | 3 | a0001c0001t0003g0038a0001c0001t0027g0084a0001c0001t0028g0042 | 3 | HG02145.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.441-2690_441-2689d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110106373 | |||||
chrX:110106373 | CT | C | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441-2689delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110106373 | |||||
chrX:110106422 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441-2658G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110106422 | ||||||
chrX:110106562 | C | T | 2 | a0001c0001t0001g0190a0001c0001t0010g0010 | 2 | HG02109.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.441-2518C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110106562 | ||||||
chrX:110106707 | A | AT | 2 | a0001c0001t0003g0087a0001c0001t0008g0101 | 2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.441-2364dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110106707 | |||||
chrX:110106788 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.441-2292T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110106788 | ||||||
chrX:110106885 | G | A | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441-2195G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110106885 | ||||||
chrX:110107134 | G | A | 12 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.441-1946G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107134 | ||||||
chrX:110107159 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.441-1921C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107159 | ||||||
chrX:110107214 | G | A | 2 | a0001c0001t0007g0013a0001c0001t0007g0014 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.441-1866G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107214 | ||||||
chrX:110107706 | C | A | 1 | a0001c0001t0011g0026 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.441-1374C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107706 | ||||||
chrX:110107706 | C | CT | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.441-1373dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110107706 | |||||
chrX:110107816 | T | C | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441-1264T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107816 | ||||||
chrX:110107950 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.441-1130G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110107950 | ||||||
chrX:110108068 | C | CTG | 27 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0105others(24): Show | 27 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.441-955_441-954dup others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTG | 39 | a0001c0001t0001g0029a0001c0001t0001g0059a0001c0001t0001g0061others(36): Show | 39 | HG00621.hp1 HG00673.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.441-957_441-954dup others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTG | 32 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0102others(29): Show | 32 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441-959_441-954dup others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(1): Show |
25 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0111others(22): Show | 25 | HG01256.hp1 HG01884.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.441-961_441-954dup others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(3): Show |
17 | a0001c0001t0001g0040a0001c0001t0001g0067a0001c0001t0001g0097others(14): Show | 17 | HG00735.hp1 HG01346.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.441-963_441-954dup others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(5): Show |
4 | a0001c0001t0002g0174a0001c0001t0003g0046a0001c0001t0004g0016others(1): Show | 4 | HG01255.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-965_441-954dup others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(7): Show |
8 | a0001c0001t0002g0056a0001c0001t0003g0043a0001c0001t0003g0089others(5): Show | 8 | HG01433.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-967_441-954dup others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(9): Show |
2 | a0001c0001t0002g0125a0001c0001t0003g0018 | 2 | HG03490.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.441-969_441-954dup others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(11): Show |
2 | a0001c0001t0003g0012a0001c0001t0022g0002 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.441-971_441-954dup others(18): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0003g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.441-973_441-954dup others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | C | CTGTGTGT others(15): Show |
1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441-975_441-954dup others(22): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTG | C | 4 | a0001c0001t0003g0049a0001c0001t0004g0011a0001c0001t0026g0141others(1): Show | 4 | HG01109.hp1 HG01346.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-955_441-954del others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTG | C | 1 | a0001c0001t0002g0070 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.441-957_441-954del others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTG | C | 2 | a0001c0001t0010g0091a0001c0001t0027g0084 | 2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.441-959_441-954del others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTGT others(1): Show |
C | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.441-961_441-954del others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441-963_441-954del others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0004g0003a0001c0001t0004g0037 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.441-965_441-954del others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTGT others(9): Show |
C | 4 | a0001c0001t0005g0175a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-969_441-954del others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108068 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-973_441-954del others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108068 | |||||
chrX:110108123 | T | TGTGTGA | 3 | a0001c0001t0006g0118a0001c0001t0006g0140a0001c0001t0006g0150 | 3 | NA18959.hp1 NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.441-954_441-953ins others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108123 | |||||
chrX:110108142 | A | G | 9 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(6): Show | 9 | HG01106.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.441-938A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108142 | ||||||
chrX:110108183 | G | A | 2 | a0001c0001t0007g0006a0001c0001t0010g0035 | 2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.441-897G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108183 | ||||||
chrX:110108215 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441-865G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108215 | ||||||
chrX:110108244 | T | C | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.441-836T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108244 | ||||||
chrX:110108359 | C | T | 21 | a0001c0001t0002g0063a0001c0001t0002g0069a0001c0001t0002g0070others(18): Show | 21 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.441-721C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108359 | ||||||
chrX:110108593 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441-487G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108593 | ||||||
chrX:110108602 | G | GT | 1 | a0001c0001t0001g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.441-476dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 110108602 | |||||
chrX:110108722 | C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18971.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.441-358C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110108722 | ||||||
chrX:110109071 | C | T | 9 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(6): Show | 9 | HG01106.hp1 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.441-9C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110109071 | ||||||
chrX:110109074 | C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0174 | 2 | HG00738.hp1 HG01255.hp1 |
splice_region_variant&intron_variant | LOW | c.441-6C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 3/6 | chrX | 110109074 | ||||||
chrX:110109244 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.507+98G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110109244 | ||||||
chrX:110109264 | TC | T | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.507+121delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110109264 | |||||
chrX:110109602 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.507+456C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110109602 | ||||||
chrX:110109605 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.507+459G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110109605 | ||||||
chrX:110109799 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.507+653C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110109799 | ||||||
chrX:110110314 | C | T | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+1168C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110110314 | ||||||
chrX:110110498 | G | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.507+1352G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110110498 | ||||||
chrX:110110607 | C | T | 5 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+1461C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110110607 | ||||||
chrX:110110788 | G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+1642G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110110788 | ||||||
chrX:110110798 | C | T | 1 | a0001c0001t0013g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.507+1652C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110110798 | ||||||
chrX:110111535 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+2389T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110111535 | ||||||
chrX:110111709 | T | A | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0063others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.507+2563T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110111709 | ||||||
chrX:110111785 | A | C | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+2639A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110111785 | ||||||
chrX:110111793 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.507+2647C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110111793 | ||||||
chrX:110111900 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.507+2754G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110111900 | ||||||
chrX:110112409 | G | A | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.507+3263G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110112409 | ||||||
chrX:110112434 | T | C | 12 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+3288T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110112434 | ||||||
chrX:110112452 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507+3306C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110112452 | ||||||
chrX:110112860 | T | C | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.507+3714T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110112860 | ||||||
chrX:110113026 | TCCTCCCT others(1): Show |
T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507+3887_507+3894d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110113026 | |||||
chrX:110113228 | C | T | 7 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+4082C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110113228 | ||||||
chrX:110113261 | T | C | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4115T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110113261 | ||||||
chrX:110113358 | G | T | 1 | a0001c0001t0025g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.507+4212G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110113358 | ||||||
chrX:110114094 | T | C | 4 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+4948T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110114094 | ||||||
chrX:110114254 | A | G | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+5108A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110114254 | ||||||
chrX:110115579 | G | T | 54 | a0001c0001t0002g0041a0001c0001t0002g0056a0001c0001t0002g0063others(51): Show | 54 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.507+6433G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110115579 | ||||||
chrX:110115865 | G | C | 1 | a0001c0001t0004g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.507+6719G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110115865 | ||||||
chrX:110116073 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.507+6927G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116073 | ||||||
chrX:110116295 | C | T | 14 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.507+7149C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116295 | ||||||
chrX:110116303 | T | G | 1 | a0001c0001t0021g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.507+7157T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116303 | ||||||
chrX:110116313 | A | G | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.507+7167A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116313 | ||||||
chrX:110116385 | T | C | 7 | a0001c0001t0003g0036a0001c0001t0003g0046a0001c0001t0003g0048others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+7239T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116385 | ||||||
chrX:110116523 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.507+7377A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116523 | ||||||
chrX:110116524 | T | C | 13 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.507+7378T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116524 | ||||||
chrX:110116822 | T | TTG | 5 | a0001c0001t0001g0122a0001c0001t0001g0156a0001c0001t0004g0045others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+7705_507+7706d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116822 | |||||
chrX:110116822 | T | TTGTG | 1 | a0001c0001t0001g0097 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.507+7703_507+7706d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116822 | |||||
chrX:110116822 | TTG | T | 12 | a0001c0001t0001g0115a0001c0001t0001g0137a0001c0001t0001g0159others(9): Show | 12 | HG00673.hp1 HG02074.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.507+7705_507+7706d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116822 | |||||
chrX:110116822 | TTGTG | T | 4 | a0001c0001t0002g0121a0001c0001t0004g0007a0001c0001t0007g0014others(1): Show | 4 | HG02155.hp2 HG03098.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+7703_507+7706d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116822 | |||||
chrX:110116822 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.507+7697_507+7706d others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116822 | |||||
chrX:110116845 | T | C | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7699T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116845 | ||||||
chrX:110116847 | T | C | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7701T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116847 | ||||||
chrX:110116851 | T | C | 12 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+7705T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116851 | ||||||
chrX:110116855 | C | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7709C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116855 | ||||||
chrX:110116861 | C | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7715C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116861 | ||||||
chrX:110116868 | GT | G | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7723delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110116868 | ||||||
chrX:110116875 | TG | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+7731delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116875 | |||||
chrX:110116876 | G | GGT | 5 | a0001c0001t0002g0098a0001c0001t0003g0012a0001c0001t0004g0007others(2): Show | 5 | HG01515.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+7754_507+7755d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116876 | |||||
chrX:110116876 | G | GGTGT | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+7752_507+7755d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116876 | |||||
chrX:110116876 | GGT | G | 5 | a0001c0001t0001g0117a0001c0001t0002g0083a0001c0001t0009g0031others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+7754_507+7755d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116876 | |||||
chrX:110116876 | GGTGT | G | 1 | a0001c0001t0002g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.507+7752_507+7755d others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116876 | |||||
chrX:110116876 | GGTGTGT | G | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.507+7750_507+7755d others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116876 | |||||
chrX:110116903 | AG | A | 8 | a0001c0001t0004g0016a0001c0001t0004g0045a0001c0001t0004g0051others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+7763delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110116903 | |||||
chrX:110117052 | G | A | 14 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.507+7906G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110117052 | ||||||
chrX:110117631 | TA | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+8490delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110117631 | |||||
chrX:110117835 | A | T | 1 | a0001c0001t0004g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.507+8689A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110117835 | ||||||
chrX:110118351 | T | G | 1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.507+9205T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110118351 | ||||||
chrX:110118394 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.507+9248G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110118394 | ||||||
chrX:110118429 | C | CA | 15 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0008others(12): Show | 15 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.507+9289dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110118429 | |||||
chrX:110118745 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.507+9599G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110118745 | ||||||
chrX:110118816 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.507+9670G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110118816 | ||||||
chrX:110118922 | G | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.507+9776G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110118922 | ||||||
chrX:110119313 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.507+10167G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119313 | ||||||
chrX:110119452 | GA | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.507+10307delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119452 | ||||||
chrX:110119643 | G | A | 4 | a0001c0001t0010g0091a0001c0001t0011g0009a0001c0001t0011g0026others(1): Show | 4 | HG02258.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+10497G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119643 | ||||||
chrX:110119711 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.507+10565G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119711 | ||||||
chrX:110119741 | G | A | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+10595G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119741 | ||||||
chrX:110119797 | A | G | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.507+10651A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110119797 | ||||||
chrX:110120036 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507+10890G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110120036 | ||||||
chrX:110120468 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.507+11322T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110120468 | ||||||
chrX:110121297 | T | C | 1 | a0001c0001t0013g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.507+12151T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110121297 | ||||||
chrX:110121519 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.507+12373A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110121519 | ||||||
chrX:110121719 | G | C | 9 | a0001c0001t0004g0034a0001c0001t0009g0031a0001c0001t0009g0032others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+12573G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110121719 | ||||||
chrX:110121894 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.507+12748C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110121894 | ||||||
chrX:110121940 | G | GT | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+12797dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110121940 | |||||
chrX:110122032 | A | T | 89 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.507+12886A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122032 | ||||||
chrX:110122067 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.507+12921G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122067 | ||||||
chrX:110122214 | G | A | 8 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+13068G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122214 | ||||||
chrX:110122360 | G | C | 1 | a0001c0001t0008g0078 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.507+13214G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122360 | ||||||
chrX:110122730 | T | C | 88 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.507+13584T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122730 | ||||||
chrX:110122868 | A | G | 3 | a0001c0001t0006g0118a0001c0001t0006g0140a0001c0001t0006g0150 | 3 | NA18959.hp1 NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.507+13722A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110122868 | ||||||
chrX:110123153 | A | T | 89 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(86): Show | 89 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.507+14007A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110123153 | ||||||
chrX:110123715 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507+14569C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110123715 | ||||||
chrX:110124088 | G | A | 73 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(70): Show | 73 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.507+14942G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124088 | ||||||
chrX:110124121 | T | TGGAA | 4 | a0001c0001t0001g0188a0001c0001t0003g0046a0001c0001t0003g0062others(1): Show | 4 | HG01109.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+15030_507+1503 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124121 | |||||
chrX:110124121 | T | TGGAAGGA others(1): Show |
3 | a0001c0001t0003g0036a0001c0001t0003g0052a0001c0001t0003g0055 | 3 | HG02572.hp1 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.507+15026_507+1503 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124121 | |||||
chrX:110124121 | T | TGGAAGGA others(5): Show |
1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.507+15022_507+1503 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124121 | |||||
chrX:110124121 | TGGAA | T | 10 | a0001c0001t0002g0069a0001c0001t0002g0103a0001c0001t0002g0104others(7): Show | 10 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.507+15030_507+1503 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124121 | |||||
chrX:110124121 | TGGAAGGA others(5): Show |
T | 3 | a0001c0001t0002g0085a0001c0001t0002g0162a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.507+15022_507+1503 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124121 | |||||
chrX:110124130 | G | GGAAGGAA others(9): Show |
1 | a0001c0001t0001g0178 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.507+14999_507+1500 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124130 | |||||
chrX:110124164 | A | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507+15018A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124164 | ||||||
chrX:110124168 | A | AAGGC | 2 | a0001c0001t0004g0094a0001c0001t0023g0096 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+15025_507+1502 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124168 | |||||
chrX:110124168 | A | C | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507+15022A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124168 | ||||||
chrX:110124172 | A | AAGGAAGG others(13): Show |
1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507+15033_507+1503 others(24): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124172 | |||||
chrX:110124172 | A | AAGGC | 5 | a0001c0001t0001g0114a0001c0001t0003g0028a0001c0001t0004g0016others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+15029_507+1503 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124172 | |||||
chrX:110124172 | A | AAGGCAGG others(1): Show |
2 | a0001c0001t0004g0045a0001c0001t0004g0054 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.507+15029_507+1503 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124172 | |||||
chrX:110124172 | A | C | 3 | a0001c0001t0004g0007a0001c0001t0004g0094a0001c0001t0023g0096 | 3 | HG02055.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.507+15026A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124172 | ||||||
chrX:110124176 | A | AAGGAAGG others(9): Show |
1 | a0001c0001t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.507+15033_507+1503 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGAAGG others(5): Show |
13 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG01496.hp2 HG01978.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.507+15033_507+1503 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGAAGG others(1): Show |
46 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0066others(43): Show | 46 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.507+15033_507+1503 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGAAGG others(5): Show |
7 | a0001c0001t0001g0079a0001c0001t0001g0102a0001c0001t0001g0126others(4): Show | 7 | HG00408.hp1 HG02071.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+15033_507+1503 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGAAGG others(9): Show |
1 | a0001c0001t0004g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.507+15033_507+1503 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGC | 55 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0105others(52): Show | 55 | HG00673.hp1 HG01074.hp1 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.507+15034_507+1503 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | AAGGCAGG others(1): Show |
9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0123others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+15037_507+1503 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124176 | |||||
chrX:110124176 | A | C | 52 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0111others(49): Show | 52 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.507+15030A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124176 | ||||||
chrX:110124184 | A | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.507+15038A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124184 | ||||||
chrX:110124184 | AAGGC | A | 1 | a0001c0001t0005g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.507+15062_507+1506 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124184 | |||||
chrX:110124188 | C | CAGGA | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.507+15045_507+1504 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124188 | |||||
chrX:110124229 | T | TG | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.507+15085dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110124229 | |||||
chrX:110124444 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.507+15298G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124444 | ||||||
chrX:110124581 | C | A | 196 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.507+15435C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124581 | ||||||
chrX:110124629 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.507+15483G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110124629 | ||||||
chrX:110125348 | C | T | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+16202C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110125348 | ||||||
chrX:110125481 | G | A | 81 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(78): Show | 81 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.507+16335G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110125481 | ||||||
chrX:110125565 | G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0133others(1): Show | 4 | HG02135.hp1 NA18944.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+16419G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110125565 | ||||||
chrX:110125566 | G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0133others(1): Show | 4 | HG02135.hp1 NA18944.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+16420G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110125566 | ||||||
chrX:110125659 | C | CT | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.507+16514dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110125659 | |||||
chrX:110125694 | G | C | 2 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.507+16548G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110125694 | ||||||
chrX:110126147 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.507+17001G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126147 | ||||||
chrX:110126198 | G | GT | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.507+17053dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126198 | |||||
chrX:110126264 | A | G | 4 | a0001c0001t0004g0034a0001c0001t0007g0006a0001c0001t0007g0019others(1): Show | 4 | HG01106.hp1 HG01243.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+17118A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126264 | ||||||
chrX:110126350 | C | A | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.507+17204C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126350 | ||||||
chrX:110126508 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.507+17362C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126508 | ||||||
chrX:110126688 | T | C | 86 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.507+17542T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126688 | ||||||
chrX:110126732 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.507+17586G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110126732 | ||||||
chrX:110126810 | C | CTG | 18 | a0001c0001t0002g0015a0001c0001t0002g0083a0001c0001t0002g0103others(15): Show | 18 | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.507+17717_507+1771 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | C | CTGTG | 12 | a0001c0001t0002g0056a0001c0001t0002g0063a0001c0001t0002g0075others(9): Show | 12 | HG01433.hp1 HG01978.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+17715_507+1771 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | C | CTGTGTG | 4 | a0001c0001t0003g0021a0001c0001t0003g0036a0001c0001t0004g0094others(1): Show | 4 | HG02486.hp1 HG02572.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+17713_507+1771 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0003g0027a0001c0001t0004g0045a0001c0001t0024g0001others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+17711_507+1771 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0002g0116a0001c0001t0003g0062 | 2 | HG01943.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.507+17709_507+1771 others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0003g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.507+17707_507+1771 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTG | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0002g0041others(9): Show | 12 | HG00140.hp1 HG01255.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.507+17717_507+1771 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTG | C | 14 | a0001c0001t0001g0040a0001c0001t0001g0127a0001c0001t0001g0144others(11): Show | 14 | HG01099.hp1 HG01256.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.507+17715_507+1771 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTG | C | 73 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0058others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.507+17713_507+1771 others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTGT others(1): Show |
C | 20 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0114others(17): Show | 20 | HG01346.hp1 HG01891.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.507+17711_507+1771 others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.507+17709_507+1771 others(14): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0007g0014a0001c0001t0023g0096 | 2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507+17707_507+1771 others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0004g0034a0001c0001t0010g0035 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.507+17705_507+1771 others(18): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126810 | CTGTGTGT others(9): Show |
C | 6 | a0001c0001t0002g0070a0001c0001t0002g0076a0001c0001t0002g0109others(3): Show | 6 | NA18522.hp1 NA18957.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+17703_507+1771 others(20): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126810 | |||||
chrX:110126859 | TGTGTG | T | 1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.507+17718_507+1772 others(9): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110126859 | |||||
chrX:110127262 | C | G | 1 | a0001c0001t0004g0003 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.508-17536C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110127262 | ||||||
chrX:110127391 | TA | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.508-17405delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110127391 | |||||
chrX:110127402 | AC | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.508-17395delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110127402 | ||||||
chrX:110127513 | C | CAAACA | 1 | a0001c0001t0002g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.508-17258_508-1725 others(9): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110127513 | |||||
chrX:110127513 | CAAACA | C | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.508-17258_508-1725 others(9): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110127513 | |||||
chrX:110127883 | G | A | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508-16915G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110127883 | ||||||
chrX:110127915 | G | A | 1 | a0001c0001t0008g0078 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.508-16883G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110127915 | ||||||
chrX:110128189 | TC | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.508-16604delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110128189 | |||||
chrX:110128429 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.508-16369A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128429 | ||||||
chrX:110128563 | G | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-16235G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128563 | ||||||
chrX:110128564 | G | A | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.508-16234G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128564 | ||||||
chrX:110128636 | A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0102 | 2 | HG00408.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.508-16162A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128636 | ||||||
chrX:110128926 | C | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0116a0001c0001t0002g0136others(2): Show | 5 | HG00408.hp2 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.508-15872C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128926 | ||||||
chrX:110128970 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508-15828G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110128970 | ||||||
chrX:110129112 | C | CT | 103 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.508-15685dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110129112 | |||||
chrX:110129218 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-15580T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110129218 | ||||||
chrX:110129497 | T | C | 2 | a0001c0001t0004g0007a0001c0001t0007g0006 | 2 | HG01106.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.508-15301T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110129497 | ||||||
chrX:110130234 | T | A | 2 | a0001c0001t0011g0009a0001c0001t0011g0026 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.508-14564T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110130234 | ||||||
chrX:110130681 | CT | C | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-14102delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110130681 | |||||
chrX:110130821 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-13977G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110130821 | ||||||
chrX:110130900 | A | G | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.508-13898A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110130900 | ||||||
chrX:110131236 | G | C | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.508-13562G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110131236 | ||||||
chrX:110131257 | C | A | 1 | a0001c0001t0002g0167 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.508-13541C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110131257 | ||||||
chrX:110131653 | C | CT | 4 | a0001c0001t0004g0034a0001c0001t0007g0006a0001c0001t0007g0019others(1): Show | 4 | HG01106.hp1 HG01243.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-13143dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110131653 | |||||
chrX:110131882 | A | G | 86 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.508-12916A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110131882 | ||||||
chrX:110131891 | A | G | 1 | a0001c0001t0006g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.508-12907A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110131891 | ||||||
chrX:110131973 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.508-12825C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110131973 | ||||||
chrX:110132179 | T | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0152a0001c0001t0005g0100 | 3 | HG00621.hp1 HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.508-12619T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110132179 | ||||||
chrX:110132326 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.508-12472G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110132326 | ||||||
chrX:110132430 | G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.508-12368G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110132430 | ||||||
chrX:110132753 | GT | G | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.508-12040delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110132753 | |||||
chrX:110132994 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.508-11804C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110132994 | ||||||
chrX:110133156 | G | GT | 7 | a0001c0001t0004g0045a0001c0001t0004g0051a0001c0001t0004g0054others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-11635dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110133156 | |||||
chrX:110133431 | A | G | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.508-11367A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110133431 | ||||||
chrX:110133451 | C | T | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.508-11347C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110133451 | ||||||
chrX:110133772 | C | A | 83 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.508-11026C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110133772 | ||||||
chrX:110134079 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.508-10719G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134079 | ||||||
chrX:110134091 | G | A | 84 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.508-10707G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134091 | ||||||
chrX:110134323 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-10475G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134323 | ||||||
chrX:110134393 | T | TAC | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.508-10391_508-1039 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134393 | |||||
chrX:110134559 | C | CA | 20 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0102others(17): Show | 20 | HG00673.hp1 HG00735.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.508-10213dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134559 | C | CAAA | 1 | a0001c0001t0008g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-10215_508-1021 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134559 | CA | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | HG01069.hp1 HG01256.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-10213delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134559 | CAA | C | 44 | a0001c0001t0002g0083a0001c0001t0002g0085a0001c0001t0002g0103others(41): Show | 44 | HG00738.hp1 HG01099.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.508-10214_508-1021 others(6): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134559 | CAAA | C | 34 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.508-10215_508-1021 others(7): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134559 | CAAAA | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0116 | 2 | HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.508-10216_508-1021 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110134559 | |||||
chrX:110134599 | C | A | 3 | a0001c0001t0004g0003a0001c0001t0004g0008a0001c0001t0004g0037 | 3 | HG02451.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.508-10199C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134599 | ||||||
chrX:110134605 | CG | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-10192delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134605 | ||||||
chrX:110134606 | G | A | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508-10192G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134606 | ||||||
chrX:110134891 | A | T | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.508-9907A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110134891 | ||||||
chrX:110135064 | A | AT | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508-9734_508-9733i others(3): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135064 | ||||||
chrX:110135065 | AT | A | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.508-9732delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135065 | ||||||
chrX:110135237 | T | TA | 6 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-9550dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110135237 | |||||
chrX:110135237 | TA | T | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.508-9550delA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110135237 | |||||
chrX:110135451 | A | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-9347A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135451 | ||||||
chrX:110135682 | G | GT | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.508-9111dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110135682 | |||||
chrX:110135734 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.508-9064G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135734 | ||||||
chrX:110135881 | A | T | 1 | a0001c0001t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508-8917A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135881 | ||||||
chrX:110135992 | G | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-8806G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110135992 | ||||||
chrX:110136061 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.508-8737T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110136061 | ||||||
chrX:110136068 | T | C | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508-8730T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110136068 | ||||||
chrX:110136229 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-8569C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110136229 | ||||||
chrX:110136259 | C | A | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-8539C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110136259 | ||||||
chrX:110137486 | G | A | 1 | a0001c0001t0021g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.508-7312G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110137486 | ||||||
chrX:110137523 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-7275C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110137523 | ||||||
chrX:110137728 | TG | T | 1 | a0001c0001t0019g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.508-7069delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110137728 | ||||||
chrX:110138157 | G | A | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.508-6641G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110138157 | ||||||
chrX:110138186 | G | A | 3 | a0001c0001t0004g0045a0001c0001t0004g0054a0001c0001t0023g0096 | 3 | HG02055.hp1 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.508-6612G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110138186 | ||||||
chrX:110138237 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508-6561C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110138237 | ||||||
chrX:110138373 | A | G | 6 | a0001c0001t0003g0038a0001c0001t0004g0003a0001c0001t0004g0007others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-6425A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110138373 | ||||||
chrX:110138945 | A | C | 83 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(80): Show | 83 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.508-5853A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110138945 | ||||||
chrX:110139428 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.508-5370C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110139428 | ||||||
chrX:110139565 | T | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.508-5233T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110139565 | ||||||
chrX:110139797 | A | AG | 1 | a0001c0001t0006g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.508-4996dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110139797 | |||||
chrX:110140464 | G | A | 6 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-4334G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110140464 | ||||||
chrX:110140573 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.508-4225C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110140573 | ||||||
chrX:110140937 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.508-3861C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110140937 | ||||||
chrX:110141200 | C | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.508-3598C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110141200 | ||||||
chrX:110141376 | A | G | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.508-3422A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110141376 | ||||||
chrX:110141881 | TC | T | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.508-2915delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110141881 | |||||
chrX:110142371 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.508-2427G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110142371 | ||||||
chrX:110142589 | T | C | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.508-2209T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110142589 | ||||||
chrX:110143060 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.508-1738G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110143060 | ||||||
chrX:110143229 | T | G | 101 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.508-1569T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110143229 | ||||||
chrX:110143678 | G | C | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.508-1120G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110143678 | ||||||
chrX:110143768 | C | A | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.508-1030C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110143768 | ||||||
chrX:110143804 | G | GGT | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0197others(3): Show | 6 | HG02027.hp1 NA19004.hp1 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-965_508-964dup others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110143804 | |||||
chrX:110143804 | G | GGTGT | 3 | a0001c0001t0001g0114a0001c0001t0001g0146a0001c0001t0001g0149 | 3 | NA18940.hp1 NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.508-967_508-964dup others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110143804 | |||||
chrX:110143804 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.508-979_508-964dup others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110143804 | |||||
chrX:110143804 | GGT | G | 2 | a0001c0001t0007g0019a0001c0001t0024g0001 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.508-965_508-964del others(2): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110143804 | |||||
chrX:110143804 | GGTGT | G | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.508-967_508-964del others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 110143804 | |||||
chrX:110143806 | T | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0003g0038others(2): Show | 5 | HG01934.hp1 HG01981.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-992T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110143806 | ||||||
chrX:110144211 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508-587C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144211 | ||||||
chrX:110144271 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508-527A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144271 | ||||||
chrX:110144275 | A | G | 103 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(100): Show | 103 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.508-523A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144275 | ||||||
chrX:110144317 | C | T | 1 | a0001c0001t0007g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.508-481C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144317 | ||||||
chrX:110144405 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.508-393C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144405 | ||||||
chrX:110144512 | G | T | 85 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.508-286G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144512 | ||||||
chrX:110144700 | G | A | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.508-98G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144700 | ||||||
chrX:110144732 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.508-66A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 4/6 | chrX | 110144732 | ||||||
chrX:110144982 | G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.586+106G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110144982 | ||||||
chrX:110145303 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.586+427G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145303 | ||||||
chrX:110145657 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.586+781C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145657 | ||||||
chrX:110145783 | T | C | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.586+907T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145783 | ||||||
chrX:110145786 | G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.586+910G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145786 | ||||||
chrX:110145908 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+1032C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145908 | ||||||
chrX:110145924 | T | C | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0023others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+1048T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110145924 | ||||||
chrX:110146005 | C | A | 100 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(97): Show | 100 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.586+1129C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110146005 | ||||||
chrX:110146505 | C | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0024 | 3 | HG01891.hp2 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.586+1629C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110146505 | ||||||
chrX:110147261 | C | CT | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0155 | 3 | HG01069.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.586+2393dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110147261 | |||||
chrX:110147570 | C | T | 1 | a0001c0001t0004g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.586+2694C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110147570 | ||||||
chrX:110147605 | C | T | 1 | a0001c0001t0006g0186 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.586+2729C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110147605 | ||||||
chrX:110147609 | C | CT | 2 | a0001c0001t0003g0038a0001c0001t0027g0084 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.586+2742dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110147609 | |||||
chrX:110147632 | A | G | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.586+2756A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110147632 | ||||||
chrX:110147876 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.586+3000T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110147876 | ||||||
chrX:110147968 | G | A | 2 | a0001c0001t0004g0011a0001c0001t0024g0001 | 2 | HG01109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.586+3092G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110147968 | ||||||
chrX:110147971 | T | TC | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3096dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110147971 | |||||
chrX:110148242 | C | CA | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3366_586+3367i others(3): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148242 | ||||||
chrX:110148267 | T | TC | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3395dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148267 | |||||
chrX:110148298 | TG | T | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3425delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148298 | |||||
chrX:110148423 | C | T | 5 | a0001c0001t0004g0007a0001c0001t0004g0011a0001c0001t0011g0009others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+3547C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148423 | ||||||
chrX:110148471 | A | G | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+3595A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148471 | ||||||
chrX:110148509 | T | C | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0019others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+3633T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148509 | ||||||
chrX:110148529 | A | AG | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3654dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148529 | |||||
chrX:110148531 | A | T | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0019others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+3655A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148531 | ||||||
chrX:110148675 | A | AT | 11 | a0001c0001t0001g0102a0001c0001t0001g0130a0001c0001t0001g0164others(8): Show | 11 | HG00735.hp2 HG01978.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.586+3823dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148675 | AT | A | 6 | a0001c0001t0003g0027a0001c0001t0003g0043a0001c0001t0003g0044others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+3823delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148675 | ATT | A | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+3822_586+3823d others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148675 | ATTT | A | 3 | a0001c0001t0007g0013a0001c0001t0007g0019a0001c0001t0021g0017 | 3 | HG03225.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.586+3821_586+3823d others(5): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148675 | ATTTTTTT others(1): Show |
A | 16 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+3816_586+3823d others(10): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148675 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0007g0006 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.586+3814_586+3823d others(12): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148675 | |||||
chrX:110148769 | TC | T | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+3896delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148769 | |||||
chrX:110148885 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.586+4009A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110148885 | ||||||
chrX:110148984 | AT | A | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+4112delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110148984 | |||||
chrX:110149083 | GT | G | 102 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(99): Show | 102 | HG00140.hp1 HG00408.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.586+4219delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110149083 | |||||
chrX:110149176 | A | G | 12 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(9): Show | 12 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.586+4300A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110149176 | ||||||
chrX:110149453 | TG | T | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+4579delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110149453 | |||||
chrX:110149586 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+4710A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110149586 | ||||||
chrX:110149593 | GT | G | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+4719delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110149593 | |||||
chrX:110149896 | T | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+5020T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110149896 | ||||||
chrX:110149909 | T | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+5033T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110149909 | ||||||
chrX:110150185 | A | AG | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+5311dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110150185 | |||||
chrX:110150266 | G | A | 1 | a0001c0001t0004g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586+5390G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150266 | ||||||
chrX:110150326 | G | A | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+5450G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150326 | ||||||
chrX:110150414 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.586+5538A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150414 | ||||||
chrX:110150426 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.586+5550T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150426 | ||||||
chrX:110150626 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.586+5750T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150626 | ||||||
chrX:110150774 | C | G | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+5898C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150774 | ||||||
chrX:110150997 | G | A | 24 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(21): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.586+6121G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110150997 | ||||||
chrX:110151033 | T | TC | 1 | a0001c0001t0017g0179 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.586+6161dupC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110151033 | |||||
chrX:110151066 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.586+6190G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151066 | ||||||
chrX:110151271 | C | G | 12 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.586+6395C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151271 | ||||||
chrX:110151423 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+6547A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151423 | ||||||
chrX:110151442 | T | C | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.586+6566T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151442 | ||||||
chrX:110151493 | G | A | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+6617G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151493 | ||||||
chrX:110151640 | G | A | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.586+6764G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110151640 | ||||||
chrX:110152056 | C | CT | 21 | a0001c0001t0001g0079a0001c0001t0001g0102a0001c0001t0001g0177others(18): Show | 21 | HG00408.hp1 HG01109.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.586+7194dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110152056 | |||||
chrX:110152056 | CT | C | 1 | a0001c0001t0003g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586+7194delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110152056 | |||||
chrX:110152070 | T | TTG | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+7194_586+7195i others(4): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152070 | ||||||
chrX:110152142 | G | A | 2 | a0001c0001t0003g0089a0001c0001t0012g0090 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.586+7266G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152142 | ||||||
chrX:110152240 | G | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+7364G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152240 | ||||||
chrX:110152300 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586+7424C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152300 | ||||||
chrX:110152306 | G | A | 7 | a0001c0001t0003g0036a0001c0001t0003g0046a0001c0001t0003g0048others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+7430G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152306 | ||||||
chrX:110152350 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+7474A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152350 | ||||||
chrX:110152445 | A | T | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+7569A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152445 | ||||||
chrX:110152459 | AT | A | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.586+7587delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110152459 | |||||
chrX:110152744 | G | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+7868G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152744 | ||||||
chrX:110152765 | A | G | 25 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(22): Show | 25 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.586+7889A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110152765 | ||||||
chrX:110153066 | C | G | 1 | a0001c0001t0001g0185 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.586+8190C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153066 | ||||||
chrX:110153117 | C | T | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+8241C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153117 | ||||||
chrX:110153249 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.586+8373T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153249 | ||||||
chrX:110153348 | C | A | 24 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(21): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.586+8472C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153348 | ||||||
chrX:110153560 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.586+8684C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153560 | ||||||
chrX:110153732 | G | T | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.586+8856G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110153732 | ||||||
chrX:110154268 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586+9392A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110154268 | ||||||
chrX:110154797 | A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0001g0172others(1): Show | 4 | HG00735.hp1 HG01346.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+9921A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110154797 | ||||||
chrX:110154867 | C | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+9991C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110154867 | ||||||
chrX:110155060 | T | A | 24 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(21): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.586+10184T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110155060 | ||||||
chrX:110155368 | T | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0102 | 2 | HG00408.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.586+10492T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110155368 | ||||||
chrX:110155475 | G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.586+10599G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110155475 | ||||||
chrX:110156014 | C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02602.hp1 HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.586+11138C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156014 | ||||||
chrX:110156100 | G | A | 6 | a0001c0001t0002g0015a0001c0001t0002g0093a0001c0001t0002g0098others(3): Show | 6 | HG00738.hp1 HG01255.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+11224G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156100 | ||||||
chrX:110156476 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.586+11600G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156476 | ||||||
chrX:110156499 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+11623A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156499 | ||||||
chrX:110156552 | C | T | 2 | a0001c0001t0007g0013a0001c0001t0021g0017 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.586+11676C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156552 | ||||||
chrX:110156919 | C | T | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+12043C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156919 | ||||||
chrX:110156980 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.586+12104G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110156980 | ||||||
chrX:110157420 | G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0174 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.586+12544G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110157420 | ||||||
chrX:110157538 | C | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.586+12662C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110157538 | ||||||
chrX:110157552 | G | A | 1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.586+12676G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110157552 | ||||||
chrX:110157902 | G | GACTA | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.586+13027_586+1302 others(8): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110157902 | |||||
chrX:110157986 | A | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+13110A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110157986 | ||||||
chrX:110158061 | A | AT | 13 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.586+13190dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110158061 | |||||
chrX:110158191 | T | C | 37 | a0001c0001t0002g0015a0001c0001t0002g0041a0001c0001t0002g0056others(34): Show | 37 | HG00140.hp1 HG00408.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.587-13229T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110158191 | ||||||
chrX:110158847 | T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG00735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.587-12573T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110158847 | ||||||
chrX:110158947 | G | A | 26 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(23): Show | 26 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.587-12473G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110158947 | ||||||
chrX:110159179 | A | T | 1 | a0001c0001t0003g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.587-12241A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110159179 | ||||||
chrX:110159356 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.587-12064G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110159356 | ||||||
chrX:110159423 | G | T | 2 | a0001c0001t0004g0007a0001c0001t0004g0011 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.587-11997G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110159423 | ||||||
chrX:110159638 | G | A | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-11782G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110159638 | ||||||
chrX:110159858 | T | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-11562T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110159858 | ||||||
chrX:110160230 | C | T | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-11190C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110160230 | ||||||
chrX:110160533 | G | C | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.587-10887G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110160533 | ||||||
chrX:110160716 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-10704A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110160716 | ||||||
chrX:110161237 | G | A | 1 | a0001c0001t0007g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.587-10183G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110161237 | ||||||
chrX:110161478 | G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.587-9942G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110161478 | ||||||
chrX:110161545 | A | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0174 | 2 | HG00738.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.587-9875A>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110161545 | ||||||
chrX:110161990 | G | C | 1 | a0001c0001t0002g0072 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.587-9430G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110161990 | ||||||
chrX:110162139 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.587-9281T>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110162139 | ||||||
chrX:110162358 | C | A | 1 | a0001c0001t0003g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.587-9062C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110162358 | ||||||
chrX:110162507 | C | T | 1 | a0001c0001t0010g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587-8913C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110162507 | ||||||
chrX:110163268 | G | A | 1 | a0001c0001t0010g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.587-8152G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163268 | ||||||
chrX:110163499 | G | A | 1 | a0001c0001t0025g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.587-7921G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163499 | ||||||
chrX:110163516 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.587-7904G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163516 | ||||||
chrX:110163603 | A | G | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-7817A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163603 | ||||||
chrX:110163641 | T | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-7779T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163641 | ||||||
chrX:110163791 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.587-7629C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163791 | ||||||
chrX:110163992 | G | T | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.587-7428G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110163992 | ||||||
chrX:110164053 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.587-7367C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164053 | ||||||
chrX:110164587 | G | A | 24 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(21): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.587-6833G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164587 | ||||||
chrX:110164650 | T | C | 9 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.587-6770T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164650 | ||||||
chrX:110164658 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.587-6762G>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164658 | ||||||
chrX:110164736 | G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0160others(3): Show | 6 | HG00735.hp1 HG01346.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-6684G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164736 | ||||||
chrX:110164881 | AAGCAGGC others(12): Show |
A | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-6538_587-6520d others(21): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164881 | ||||||
chrX:110164902 | T | G | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-6518T>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164902 | ||||||
chrX:110164957 | G | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.587-6463G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110164957 | ||||||
chrX:110165006 | T | C | 1 | a0001c0001t0010g0010 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.587-6414T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110165006 | ||||||
chrX:110165091 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.587-6329C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110165091 | ||||||
chrX:110165169 | A | G | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-6251A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110165169 | ||||||
chrX:110165603 | C | A | 1 | a0001c0001t0001g0193 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.587-5817C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110165603 | ||||||
chrX:110165755 | T | C | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-5665T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110165755 | ||||||
chrX:110166222 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.587-5198A>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110166222 | ||||||
chrX:110166439 | G | A | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-4981G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110166439 | ||||||
chrX:110166692 | T | C | 3 | a0001c0001t0002g0085a0001c0001t0002g0162a0001c0001t0002g0174 | 3 | HG00738.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.587-4728T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110166692 | ||||||
chrX:110167235 | G | T | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.587-4185G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110167235 | ||||||
chrX:110167365 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.587-4055G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110167365 | ||||||
chrX:110167556 | C | T | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-3864C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110167556 | ||||||
chrX:110167784 | GC | G | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3632delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110167784 | |||||
chrX:110167855 | C | G | 24 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(21): Show | 24 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.587-3565C>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110167855 | ||||||
chrX:110167899 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.587-3521C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110167899 | ||||||
chrX:110167963 | T | TA | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3455dupA | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110167963 | |||||
chrX:110167984 | T | TG | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3435dupG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110167984 | |||||
chrX:110168024 | CT | C | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3393delT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110168024 | |||||
chrX:110168141 | TG | T | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3276delG | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110168141 | |||||
chrX:110168195 | G | GT | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-3224dupT | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110168195 | |||||
chrX:110168336 | T | C | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.587-3084T>C | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168336 | ||||||
chrX:110168350 | C | T | 1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.587-3070C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168350 | ||||||
chrX:110168377 | G | GAGGGTTG others(7): Show |
1 | a0001c0001t0027g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.587-3041_587-3028d others(16): Show |
TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110168377 | |||||
chrX:110168381 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.587-3039G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168381 | ||||||
chrX:110168676 | C | T | 4 | a0001c0001t0003g0065a0001c0001t0003g0113a0001c0001t0004g0034others(1): Show | 4 | HG01168.hp2 HG01258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-2744C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168676 | ||||||
chrX:110168782 | G | A | 1 | a0001c0001t0007g0014 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.587-2638G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168782 | ||||||
chrX:110168841 | G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.587-2579G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168841 | ||||||
chrX:110168928 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.587-2492C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110168928 | ||||||
chrX:110169081 | A | G | 3 | a0001c0001t0011g0009a0001c0001t0011g0026a0001c0001t0022g0002 | 3 | HG02258.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.587-2339A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110169081 | ||||||
chrX:110169105 | C | T | 7 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0003g0020others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2315C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110169105 | ||||||
chrX:110169390 | TC | T | 1 | a0003c0003t0016g0142 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.587-2024delC | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 110169390 | |||||
chrX:110169831 | G | T | 1 | a0001c0001t0005g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.587-1589G>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110169831 | ||||||
chrX:110169885 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.587-1535C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110169885 | ||||||
chrX:110170010 | C | T | 2 | a0001c0001t0003g0065a0001c0001t0003g0113 | 2 | HG01168.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.587-1410C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170010 | ||||||
chrX:110170103 | G | A | 2 | a0001c0001t0003g0089a0001c0001t0012g0090 | 2 | HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.587-1317G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170103 | ||||||
chrX:110170116 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.587-1304A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170116 | ||||||
chrX:110170910 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.587-510A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170910 | ||||||
chrX:110170951 | A | G | 16 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0008others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-469A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170951 | ||||||
chrX:110170975 | C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0117others(3): Show | 6 | HG02074.hp1 HG02132.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-445C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 5/6 | chrX | 110170975 | ||||||
chrX:110171933 | C | T | 4 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0007g0019others(1): Show | 4 | HG03225.hp1 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+413C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110171933 | ||||||
chrX:110172130 | G | A | 8 | a0001c0001t0007g0006a0001c0001t0007g0013a0001c0001t0007g0014others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+610G>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110172130 | ||||||
chrX:110172172 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.687+652A>G | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110172172 | ||||||
chrX:110172192 | C | A | 1 | a0001c0001t0024g0001 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687+672C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110172192 | ||||||
chrX:110172765 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.688-480C>A | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110172765 | ||||||
chrX:110172991 | C | T | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0033 | 3 | HG01891.hp1 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.688-254C>T | TMEM164 | ENSG00000157600.12 | transcript | ENST00000372068.7 | protein_coding | 6/6 | chrX | 110172991 |