geneid | 57187 |
---|---|
ensemblid | ENSG00000125676.20 |
hgncid | 19073 |
symbol | THOC2 |
name | THO complex subunit 2 |
refseq_nuc | NM_001081550.2 |
refseq_prot | NP_001075019.1 |
ensembl_nuc | ENST00000245838.13 |
ensembl_prot | ENSP00000245838.8 |
mane_status | MANE Select |
chr | chrX |
start | 123600569 |
end | 123733052 |
strand | - |
ver | v1.2 |
region | chrX:123600569-123733052 |
region5000 | chrX:123595569-123738052 |
regionname0 | THOC2_chrX_123600569_123733052 |
regionname5000 | THOC2_chrX_123595569_123738052 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1593 | 247 | 69 | 47 | 92 | 11 | 26 | 74 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0002 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0003 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0004 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0005 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4782 | 244 | 68 | 46 | 91 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0002 | 0/0 | 4782 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0003 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0004 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0005 | 0/0 | 4782 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0006 | 0/0 | 4782 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0007 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
c0008 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 819 | 251 | 70 | 47 | 95 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4782 | 244 | 68 | 46 | 91 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0002 | 0/0 | 4782 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0005 | 0/0 | 4782 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0007 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0002c0006 | 0/0 | 4782 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0003c0004 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0004c0008 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0005c0003 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5600 | 244 | 68 | 46 | 91 | 11 | 26 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0002t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0005t0001 | 0/0 | 5600 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0001c0007t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0002c0006t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0003c0004t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0004c0008t0001 | 0/0 | 5599 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
a0005c0003t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | copy fasta | chrX | 123595569 | 123738052 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0001c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0002c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0004c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
a0005c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0111 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02615 | hp2 | a0002 | c0006 | t0001 | g0147 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18990 | hp1 | a0005 | c0003 | t0001 | g0063 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19074 | hp1 | a0003 | c0004 | t0001 | g0236 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19077 | hp2 | a0001 | c0007 | t0001 | g0060 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19089 | hp1 | a0004 | c0008 | t0001 | g0084 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0215 | REF | REF | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | THOC2_chrX_123595569_123738052 | THOC2 | chrX | 123595569 | 123738052 |
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:123621328
|
C | T | 1 | a0003 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.4045G>A | p.Ala1349Thr | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/39 | 4075/5600 | 4045/4782 | 1349/1593 | chrX | 123621328 | ||
chrX:123622783
|
T | C | 1 | a0002 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3760A>G | p.Ser1254Gly | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 30/39 | 3790/5600 | 3760/4782 | 1254/1593 | chrX | 123622783 | ||
chrX:123627944
|
AT | A | 1 | a0004 | 1 | NA19089.hp1 | frameshift_variant | HIGH | c.2505delA | p.Lys835fs | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/39 | 2535/5600 | 2505/4782 | 835/1593 | chrX | 123627944 | ||
chrX:123665767
|
C | T | 1 | a0005 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1261G>A | p.Ala421Thr | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/39 | 1291/5600 | 1261/4782 | 421/1593 | chrX | 123665767 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:123621329
|
G | A | 1 | a0001c0005 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.4044C>T | p.Asn1348Asn | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/39 | 4074/5600 | 4044/4782 | 1348/1593 | chrX | 123621329 | ||
chrX:123623133
|
T | C | 1 | a0001c0007 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.3654A>G | p.Lys1218Lys | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 29/39 | 3684/5600 | 3654/4782 | 1218/1593 | chrX | 123623133 | ||
chrX:123667141
|
C | T | 1 | a0001c0002 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1155G>A | p.Lys385Lys | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/39 | 1185/5600 | 1155/4782 | 385/1593 | chrX | 123667141 |
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 |
---|
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:123601370
|
G | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.*19-32C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601370 | ||||||
chrX:123601485
|
A | AAGGG | 1 | a0001c0001t0001g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*19-151_*19-148dup others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601485 | ||||||
chrX:123601485
|
AAGGGAGG others(1): Show |
A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*19-155_*19-148del others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601485 | ||||||
chrX:123601582
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0220 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.*19-244A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601582 | ||||||
chrX:123601646
|
C | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.*19-308G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601646 | ||||||
chrX:123601697
|
TA | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0181 | 2 | NA19055.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.*19-360delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601697 | ||||||
chrX:123601723
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*19-385C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601723 | ||||||
chrX:123601767
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18988.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.*19-429G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601767 | ||||||
chrX:123601786
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.*19-448G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123601786 | ||||||
chrX:123602392
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.*19-1054C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602392 | ||||||
chrX:123602433
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0098 | 2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.*19-1095C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602433 | ||||||
chrX:123602455
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*19-1117G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602455 | ||||||
chrX:123602531
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.*19-1193T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602531 | ||||||
chrX:123602683
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.*19-1345G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602683 | ||||||
chrX:123602831
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0203a0001c0001t0001g0243 | 3 | NA18957.hp1 NA18987.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.*19-1493G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602831 | ||||||
chrX:123602845
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*19-1507T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123602845 | ||||||
chrX:123603013
|
G | GA | 2 | a0001c0001t0001g0099a0001c0001t0001g0107 | 2 | HG00639.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.*19-1676dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603013 | ||||||
chrX:123603077
|
C | CA | 3 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0240 | 3 | HG01943.hp1 HG02109.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.*19-1740dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603077 | ||||||
chrX:123603134
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18988.hp1 NA18989.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.*19-1796T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603134 | ||||||
chrX:123603933
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*19-2595T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123603933 | ||||||
chrX:123604026
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*19-2688C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604026 | ||||||
chrX:123604320
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*19-2982A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604320 | ||||||
chrX:123604371
|
G | GT | 2 | a0001c0001t0001g0112a0001c0001t0001g0246 | 2 | HG02109.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.*19-3034dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604371 | ||||||
chrX:123604450
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*19-3112C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604450 | ||||||
chrX:123604742
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*19-3404A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604742 | ||||||
chrX:123604756
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0030 | 2 | NA18987.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.*19-3418A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123604756 | ||||||
chrX:123605107
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.*19-3769C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605107 | ||||||
chrX:123605228
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.*19-3890A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605228 | ||||||
chrX:123605248
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.*19-3910C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605248 | ||||||
chrX:123605270
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.*19-3932A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605270 | ||||||
chrX:123605396
|
A | AT | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*19-4059dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605396 | ||||||
chrX:123605581
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*19-4243A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605581 | ||||||
chrX:123605612
|
C | CA | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*19-4275dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605612 | ||||||
chrX:123605778
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.*19-4440T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605778 | ||||||
chrX:123605907
|
TG | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0159others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.*19-4570delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123605907 | ||||||
chrX:123606171
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.*18+4747G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606171 | ||||||
chrX:123606274
|
C | CA | 15 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0118others(12): Show | 15 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.*18+4643dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606274 | ||||||
chrX:123606274
|
CA | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0200 | 2 | HG01081.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.*18+4643delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606274 | ||||||
chrX:123606286
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0177 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.*18+4632T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606286 | ||||||
chrX:123606555
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.*18+4363G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123606555 | ||||||
chrX:123607057
|
T | TA | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*18+3860dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607057 | ||||||
chrX:123607084
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.*18+3834C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607084 | ||||||
chrX:123607298
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.*18+3620G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607298 | ||||||
chrX:123607419
|
G | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*18+3499C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607419 | ||||||
chrX:123607444
|
T | TTTTA | 22 | a0001c0001t0001g0001a0001c0001t0001g0074a0001c0001t0001g0093others(19): Show | 22 | HG00738.hp1 HG01433.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.*18+3470_*18+3473d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | ||||||
chrX:123607444
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0112a0001c0001t0001g0128others(1): Show | 4 | HG02109.hp2 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.*18+3466_*18+3473d others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | ||||||
chrX:123607444
|
TTTTA | T | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.*18+3470_*18+3473d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | ||||||
chrX:123607444
|
TTTTATTT others(1): Show |
T | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG01496.hp1 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.*18+3466_*18+3473d others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | ||||||
chrX:123607444
|
TTTTATTT others(13): Show |
T | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*18+3454_*18+3473d others(22): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607444 | ||||||
chrX:123607453
|
T | TTTAG | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.*18+3464_*18+3465i others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607453 | ||||||
chrX:123607530
|
C | G | 75 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0116others(72): Show | 75 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.*18+3388G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607530 | ||||||
chrX:123607737
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*18+3181G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607737 | ||||||
chrX:123607912
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*18+3006G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123607912 | ||||||
chrX:123608362
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.*18+2556A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608362 | ||||||
chrX:123608413
|
CA | C | 1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*18+2504delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608413 | ||||||
chrX:123608417
|
A | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.*18+2501T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608417 | ||||||
chrX:123608517
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.*18+2401T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608517 | ||||||
chrX:123608519
|
T | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.*18+2399A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608519 | ||||||
chrX:123608597
|
G | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0239 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.*18+2321C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123608597 | ||||||
chrX:123609022
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*18+1896G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609022 | ||||||
chrX:123609161
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*18+1757C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609161 | ||||||
chrX:123609378
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*18+1540A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609378 | ||||||
chrX:123609628
|
C | T | 1 | a0003c0004t0001g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.*18+1290G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609628 | ||||||
chrX:123609795
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*18+1123G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609795 | ||||||
chrX:123609944
|
G | T | 9 | a0001c0001t0001g0132a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.*18+974C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123609944 | ||||||
chrX:123610028
|
C | CA | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*18+889dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610028 | ||||||
chrX:123610295
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.*18+613_*18+622del others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610295 | ||||||
chrX:123610391
|
T | TA | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0093others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.*18+526dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610391 | ||||||
chrX:123610463
|
C | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*18+455G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610463 | ||||||
chrX:123610724
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.*18+194C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 38/38 | chrX | 123610724 | ||||||
chrX:123611027
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4755-64A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 37/38 | chrX | 123611027 | ||||||
chrX:123611298
|
T | TGA | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4754+140_4754+141d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 37/38 | chrX | 123611298 | ||||||
chrX:123611364
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4754+76T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 37/38 | chrX | 123611364 | ||||||
chrX:123611682
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4678-166A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123611682 | ||||||
chrX:123611752
|
GA | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0215 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4678-237delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123611752 | ||||||
chrX:123611779
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4678-263A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123611779 | ||||||
chrX:123613207
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4677+192G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123613207 | ||||||
chrX:123613259
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0234 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4677+140G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 36/38 | chrX | 123613259 | ||||||
chrX:123613625
|
A | G | 1 | a0001c0007t0001g0060 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.4519+14T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 35/38 | chrX | 123613625 | ||||||
chrX:123614552
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-363C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614552 | ||||||
chrX:123614863
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.4312-674G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614863 | ||||||
chrX:123614925
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4312-736C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123614925 | ||||||
chrX:123615084
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-895C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615084 | ||||||
chrX:123615173
|
C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4312-984G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615173 | ||||||
chrX:123615202
|
AAATAG | A | 1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4312-1018_4312-101 others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615202 | ||||||
chrX:123615324
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4312-1135G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615324 | ||||||
chrX:123615348
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4312-1159G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615348 | ||||||
chrX:123615469
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4312-1280A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615469 | ||||||
chrX:123615528
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4312-1339A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615528 | ||||||
chrX:123615535
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4312-1346C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615535 | ||||||
chrX:123615644
|
C | CA | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.4312-1456dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615644 | ||||||
chrX:123615654
|
A | AAAAT | 2 | a0001c0001t0001g0094a0001c0001t0001g0098 | 2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.4312-1466_4312-146 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615654 | ||||||
chrX:123615654
|
A | AAAT | 4 | a0001c0001t0001g0015a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG00323.hp1 HG02738.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.4312-1466_4312-146 others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615654 | ||||||
chrX:123615654
|
A | AT | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4312-1466_4312-146 others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615654 | ||||||
chrX:123615655
|
AT | A | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4312-1467delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615655 | ||||||
chrX:123615656
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0094a0001c0001t0001g0098others(4): Show | 7 | HG00323.hp1 HG02683.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.4312-1467A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615656 | ||||||
chrX:123615656
|
T | TAC | 13 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0132others(10): Show | 13 | HG01952.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.4312-1469_4312-146 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615656 | ||||||
chrX:123615656
|
T | TACAC | 2 | a0001c0001t0001g0001a0001c0001t0001g0168 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4312-1471_4312-146 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615656 | ||||||
chrX:123615658
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4312-1469G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615658 | ||||||
chrX:123615680
|
C | CAA | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0183 | 3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4312-1493_4312-149 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123615680 | ||||||
chrX:123616100
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4312-1911G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616100 | ||||||
chrX:123616190
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4312-2001A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616190 | ||||||
chrX:123616195
|
CT | C | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4312-2007delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616195 | ||||||
chrX:123616525
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4312-2336A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616525 | ||||||
chrX:123616630
|
C | CCT | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG00280.hp1 HG02683.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.4312-2443_4312-244 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616630 | ||||||
chrX:123616673
|
G | GT | 2 | a0001c0001t0001g0013a0001c0001t0001g0115 | 2 | HG02280.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.4312-2485dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616673 | ||||||
chrX:123616673
|
GT | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0112 | 2 | HG02109.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.4312-2485delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616673 | ||||||
chrX:123616680
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4312-2491A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616680 | ||||||
chrX:123616728
|
C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4312-2539G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616728 | ||||||
chrX:123616803
|
T | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0088 | 2 | HG00438.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4311+2598A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123616803 | ||||||
chrX:123617372
|
T | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0210 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4311+2029A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123617372 | ||||||
chrX:123618187
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4311+1214A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618187 | ||||||
chrX:123618195
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4311+1206A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618195 | ||||||
chrX:123618877
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4311+524T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123618877 | ||||||
chrX:123619030
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4311+371G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619030 | ||||||
chrX:123619035
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4311+366A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619035 | ||||||
chrX:123619036
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4311+365C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619036 | ||||||
chrX:123619095
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4311+306T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619095 | ||||||
chrX:123619097
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01496.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.4311+304C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619097 | ||||||
chrX:123619141
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.4311+260A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619141 | ||||||
chrX:123619269
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4311+132A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 33/38 | chrX | 123619269 | ||||||
chrX:123619537
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4276-101A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 32/38 | chrX | 123619537 | ||||||
chrX:123619954
|
CT | C | 1 | a0001c0001t0001g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4276-519delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 32/38 | chrX | 123619954 | ||||||
chrX:123620506
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4275+401A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 32/38 | chrX | 123620506 | ||||||
chrX:123621023
|
T | TA | 1 | a0001c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4217-59dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/38 | chrX | 123621023 | ||||||
chrX:123621127
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4216+30C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 31/38 | chrX | 123621127 | ||||||
chrX:123621931
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3786-344C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 30/38 | chrX | 123621931 | ||||||
chrX:123623034
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3682+71A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 29/38 | chrX | 123623034 | ||||||
chrX:123623501
|
C | CT | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.3504-219dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 28/38 | chrX | 123623501 | ||||||
chrX:123623501
|
C | CTT | 1 | a0001c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3504-220_3504-219d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 28/38 | chrX | 123623501 | ||||||
chrX:123623501
|
CT | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0219a0001c0001t0001g0226 | 3 | HG00738.hp1 NA18952.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.3504-219delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 28/38 | chrX | 123623501 | ||||||
chrX:123624047
|
AT | A | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3318+12delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 27/38 | chrX | 123624047 | ||||||
chrX:123624444
|
TA | T | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3186+96delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 26/38 | chrX | 123624444 | ||||||
chrX:123624678
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.3058-9C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123624678 | ||||||
chrX:123624837
|
G | GT | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3058-169dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123624837 | ||||||
chrX:123624961
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3058-292A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123624961 | ||||||
chrX:123625085
|
TTTTTG | T | 1 | a0001c0001t0001g0016 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3058-421_3058-417d others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625085 | ||||||
chrX:123625115
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3058-446A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625115 | ||||||
chrX:123625187
|
G | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0089 | 2 | NA18612.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3058-518C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625187 | ||||||
chrX:123625520
|
C | CT | 2 | a0001c0001t0001g0110a0001c0001t0001g0115 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3057+391dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625520 | ||||||
chrX:123625520
|
CT | C | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0143others(4): Show | 7 | HG01168.hp1 HG01256.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3057+391delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625520 | ||||||
chrX:123625720
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3057+192T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625720 | ||||||
chrX:123625820
|
CT | C | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3057+91delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625820 | ||||||
chrX:123625884
|
CT | C | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3057+27delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 25/38 | chrX | 123625884 | ||||||
chrX:123626244
|
C | CT | 1 | a0001c0001t0001g0213 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2900-176dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 24/38 | chrX | 123626244 | ||||||
chrX:123627033
|
A | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2758-371T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627033 | ||||||
chrX:123627099
|
A | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2758-437T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627099 | ||||||
chrX:123627186
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2757+507G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627186 | ||||||
chrX:123627277
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2757+416G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627277 | ||||||
chrX:123627506
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0164 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2757+187A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627506 | ||||||
chrX:123627535
|
C | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2757+158G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 23/38 | chrX | 123627535 | ||||||
chrX:123628116
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2482-148A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628116 | ||||||
chrX:123628170
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2482-202A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628170 | ||||||
chrX:123628282
|
T | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0041others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2482-314A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628282 | ||||||
chrX:123628722
|
T | TA | 8 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0146others(5): Show | 8 | HG01978.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2482-755dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628722 | ||||||
chrX:123628722
|
TA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0065others(7): Show | 10 | HG00323.hp2 HG01074.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.2482-755delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628722 | ||||||
chrX:123628785
|
C | CT | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-818dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628785 | ||||||
chrX:123628862
|
TG | T | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-895delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628862 | ||||||
chrX:123628945
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0221 | 2 | NA18959.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.2482-977A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628945 | ||||||
chrX:123628980
|
C | CT | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-1013dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123628980 | ||||||
chrX:123629010
|
TG | T | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-1043delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629010 | ||||||
chrX:123629053
|
G | GA | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2482-1086dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629053 | ||||||
chrX:123629099
|
G | GC | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-1132dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629099 | ||||||
chrX:123629139
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2482-1171T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629139 | ||||||
chrX:123629206
|
A | AAC | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 56 | HG00741.hp1 HG01074.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.2482-1240_2482-123 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACAC | 30 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0059others(27): Show | 30 | HG00438.hp2 HG00673.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.2482-1242_2482-123 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACAC | 18 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0068others(15): Show | 18 | HG00735.hp2 HG01167.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.2482-1244_2482-123 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACACA others(1): Show |
41 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0019others(38): Show | 41 | HG01258.hp1 HG01934.hp1 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.2482-1246_2482-123 others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACACA others(3): Show |
26 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2482-1248_2482-123 others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACACA others(5): Show |
19 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(16): Show | 19 | HG00140.hp1 HG00438.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.2482-1250_2482-123 others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACACA others(7): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0096 | 3 | HG00621.hp1 HG03195.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2482-1252_2482-123 others(18): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0030 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2482-1254_2482-123 others(20): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
AAC | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0122others(10): Show | 13 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2482-1240_2482-123 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
AACAC | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(5): Show | 8 | HG01243.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2482-1242_2482-123 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
AACACAC | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0160 | 2 | HG01106.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2482-1244_2482-123 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629206
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2482-1252_2482-123 others(18): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629206 | ||||||
chrX:123629244
|
CACAT | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2482-1280_2482-127 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629244 | ||||||
chrX:123629246
|
C | CACACACA others(5): Show |
1 | a0001c0001t0001g0026 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2482-1279_2482-127 others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629246 | ||||||
chrX:123629246
|
C | CACACAT | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2482-1279_2482-127 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629246 | ||||||
chrX:123629248
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0207a0001c0001t0001g0248 | 3 | HG02148.hp2 HG02630.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2482-1280A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629248 | ||||||
chrX:123629261
|
AAC | A | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2482-1295_2482-129 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629261 | ||||||
chrX:123629570
|
A | AT | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-1603dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629570 | ||||||
chrX:123629653
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2482-1685C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629653 | ||||||
chrX:123629753
|
TA | T | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2482-1786delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629753 | ||||||
chrX:123629835
|
CG | C | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1852delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629835 | ||||||
chrX:123629865
|
TA | T | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1822delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629865 | ||||||
chrX:123629922
|
A | AAG | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1765_2481+176 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629922 | ||||||
chrX:123629923
|
G | C | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1765C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629923 | ||||||
chrX:123629929
|
CT | C | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1758delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123629929 | ||||||
chrX:123630387
|
C | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+1301G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630387 | ||||||
chrX:123630481
|
C | CG | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+1206dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630481 | ||||||
chrX:123630612
|
C | CA | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(82): Show | 85 | HG01069.hp1 HG01099.hp1 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.2481+1075dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630612
|
C | CAA | 16 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0077others(13): Show | 16 | HG00438.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2481+1074_2481+107 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630612
|
C | CAAA | 3 | a0001c0001t0001g0180a0001c0001t0001g0195a0001c0001t0001g0201 | 3 | HG01433.hp1 HG02148.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2481+1073_2481+107 others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630612
|
C | CAAAA | 2 | a0001c0001t0001g0187a0001c0001t0001g0248 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2481+1072_2481+107 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630612
|
CA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0075a0001c0001t0001g0151others(3): Show | 6 | HG00639.hp1 HG01168.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+1075delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630612
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2481+1065_2481+107 others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630612 | ||||||
chrX:123630706
|
C | A | 9 | a0001c0001t0001g0132a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2481+982G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123630706 | ||||||
chrX:123631039
|
G | GC | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2481+648dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631039 | ||||||
chrX:123631072
|
C | G | 75 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0127others(72): Show | 75 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.2481+616G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631072 | ||||||
chrX:123631217
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2481+471A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631217 | ||||||
chrX:123631267
|
C | T | 9 | a0001c0001t0001g0136a0001c0001t0001g0203a0001c0001t0001g0216others(6): Show | 9 | NA18943.hp1 NA18957.hp1 NA18987.hp1 others(6): Show |
intron_variant | MODIFIER | c.2481+421G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631267 | ||||||
chrX:123631598
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2481+90G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 22/38 | chrX | 123631598 | ||||||
chrX:123631899
|
T | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2317-47A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123631899 | ||||||
chrX:123632001
|
C | CA | 1 | a0001c0001t0001g0214 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2317-150dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632001 | ||||||
chrX:123632297
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2317-445C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632297 | ||||||
chrX:123632319
|
C | A | 1 | a0004c0008t0001g0084 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2317-467G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632319 | ||||||
chrX:123632401
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2316+460A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632401 | ||||||
chrX:123632489
|
C | CA | 8 | a0001c0001t0001g0134a0001c0001t0001g0165a0001c0001t0001g0188others(5): Show | 8 | HG00438.hp2 HG01928.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2316+371dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | ||||||
chrX:123632489
|
C | CAA | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2316+370_2316+371d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | ||||||
chrX:123632489
|
C | CAAA | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.2316+369_2316+371d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | ||||||
chrX:123632489
|
CA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2316+371delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | ||||||
chrX:123632489
|
CAA | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG01099.hp1 HG01106.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2316+370_2316+371d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632489 | ||||||
chrX:123632587
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | HG02148.hp1 NA18942.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2316+274G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632587 | ||||||
chrX:123632692
|
T | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2316+169A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 21/38 | chrX | 123632692 | ||||||
chrX:123633081
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2137-41A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633081 | ||||||
chrX:123633341
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2137-301C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633341 | ||||||
chrX:123633346
|
A | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0183 | 3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2137-306T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633346 | ||||||
chrX:123633362
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2137-322A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633362 | ||||||
chrX:123633391
|
TTTTA | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2137-355_2137-352d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633391 | ||||||
chrX:123633411
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2137-371A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633411 | ||||||
chrX:123633489
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2137-449C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633489 | ||||||
chrX:123633696
|
GC | G | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2136+256delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633696 | ||||||
chrX:123633765
|
CT | C | 2 | a0001c0001t0001g0221a0002c0006t0001g0147 | 2 | HG02615.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.2136+187delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633765 | ||||||
chrX:123633808
|
AGGGG | A | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2136+141_2136+144d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 20/38 | chrX | 123633808 | ||||||
chrX:123634432
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2019-362T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634432 | ||||||
chrX:123634631
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2019-561A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634631 | ||||||
chrX:123634900
|
G | GA | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2019-831dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634900 | ||||||
chrX:123634981
|
G | GT | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2019-912dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123634981 | ||||||
chrX:123635103
|
G | GT | 6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0021others(3): Show | 6 | HG01978.hp2 HG02293.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018+975dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635103 | ||||||
chrX:123635343
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2018+736T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635343 | ||||||
chrX:123635346
|
GT | G | 3 | a0001c0001t0001g0196a0001c0001t0001g0209a0001c0001t0001g0211 | 3 | NA19002.hp2 NA19068.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2018+732delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635346 | ||||||
chrX:123635594
|
GA | G | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2018+484delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 19/38 | chrX | 123635594 | ||||||
chrX:123636473
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0239 | 2 | HG01891.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1922-298C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636473 | ||||||
chrX:123636593
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1922-418G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636593 | ||||||
chrX:123636944
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1922-769C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123636944 | ||||||
chrX:123637140
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0203a0001c0001t0001g0216others(6): Show | 9 | NA18943.hp1 NA18957.hp1 NA18987.hp1 others(6): Show |
intron_variant | MODIFIER | c.1921+903C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637140 | ||||||
chrX:123637223
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1921+820A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637223 | ||||||
chrX:123637238
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1921+805G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637238 | ||||||
chrX:123637263
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1921+780C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637263 | ||||||
chrX:123637365
|
CAA | C | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1921+676_1921+677d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637365 | ||||||
chrX:123637497
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921+546T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637497 | ||||||
chrX:123637641
|
TC | T | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1921+401delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637641 | ||||||
chrX:123637760
|
G | GA | 1 | a0001c0001t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1921+282dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 18/38 | chrX | 123637760 | ||||||
chrX:123638666
|
C | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0151 | 2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1840+268G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638666 | ||||||
chrX:123638666
|
C | CA | 1 | a0001c0001t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1840+267dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638666 | ||||||
chrX:123638668
|
A | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1840+266T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638668 | ||||||
chrX:123638726
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1840+208C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638726 | ||||||
chrX:123638727
|
T | TAC | 24 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(21): Show | 24 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1840+205_1840+206d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638727 | ||||||
chrX:123638727
|
TAC | T | 15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(12): Show | 15 | HG01192.hp1 HG01346.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1840+205_1840+206d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638727 | ||||||
chrX:123638735
|
C | CGT | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1840+198_1840+199i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638735 | ||||||
chrX:123638743
|
C | CA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1840+190dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638743 | ||||||
chrX:123638750
|
A | ACT | 6 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG01106.hp1 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840+182_1840+183d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | ||||||
chrX:123638750
|
A | ACTCT | 3 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1840+180_1840+183d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | ||||||
chrX:123638750
|
A | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0068others(2): Show | 5 | HG02602.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1840+184T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | ||||||
chrX:123638750
|
ACT | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1840+182_1840+183d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | ||||||
chrX:123638750
|
ACTCTCT | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1840+178_1840+183d others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638750 | ||||||
chrX:123638764
|
T | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1840+170A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638764 | ||||||
chrX:123638767
|
C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1840+167G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638767 | ||||||
chrX:123638769
|
T | C | 2 | a0001c0001t0001g0047a0001c0005t0001g0111 | 2 | HG01496.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1840+165A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | ||||||
chrX:123638769
|
T | TAC | 15 | a0001c0001t0001g0019a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG01099.hp1 HG01106.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1840+163_1840+164d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | ||||||
chrX:123638769
|
TAC | T | 6 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG01175.hp2 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1840+163_1840+164d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | ||||||
chrX:123638769
|
TACAC | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1840+161_1840+164d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 17/38 | chrX | 123638769 | ||||||
chrX:123639154
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1747-127A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639154 | ||||||
chrX:123639392
|
T | TC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1747-366dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639392 | ||||||
chrX:123639419
|
AT | A | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1747-393delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639419 | ||||||
chrX:123639486
|
G | C | 6 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747-459C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639486 | ||||||
chrX:123639499
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1747-472A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639499 | ||||||
chrX:123639646
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 38 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.1747-619C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639646 | ||||||
chrX:123639790
|
C | A | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1746+748G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639790 | ||||||
chrX:123639902
|
TG | T | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1746+635delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639902 | ||||||
chrX:123639991
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1746+547C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123639991 | ||||||
chrX:123640004
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1746+534C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640004 | ||||||
chrX:123640044
|
A | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1746+494T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640044 | ||||||
chrX:123640060
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1746+478C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640060 | ||||||
chrX:123640127
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1746+411G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640127 | ||||||
chrX:123640287
|
A | ACCT | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1746+250_1746+251i others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640287 | ||||||
chrX:123640315
|
T | C | 1 | a0003c0004t0001g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1746+223A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640315 | ||||||
chrX:123640333
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1746+205T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640333 | ||||||
chrX:123640457
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1746+81G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 16/38 | chrX | 123640457 | ||||||
chrX:123640700
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1662-78C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123640700 | ||||||
chrX:123640706
|
G | GA | 1 | a0001c0001t0001g0055 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1662-85dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123640706 | ||||||
chrX:123641033
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1662-411A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641033 | ||||||
chrX:123641104
|
A | AAT | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662-483_1662-482i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641104 | ||||||
chrX:123641370
|
T | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1662-748A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641370 | ||||||
chrX:123641436
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1662-814G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641436 | ||||||
chrX:123641608
|
A | AC | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1662-987dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123641608 | ||||||
chrX:123642087
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1662-1465G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642087 | ||||||
chrX:123642099
|
T | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1662-1477A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642099 | ||||||
chrX:123642164
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662-1542C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642164 | ||||||
chrX:123642219
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1662-1597A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642219 | ||||||
chrX:123642286
|
T | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662-1664A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642286 | ||||||
chrX:123642380
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0053 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1662-1758C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642380 | ||||||
chrX:123642386
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1662-1764G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642386 | ||||||
chrX:123642429
|
C | CA | 6 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0080others(3): Show | 6 | HG00438.hp1 HG02074.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662-1808dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642429 | ||||||
chrX:123642429
|
CA | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0157a0001c0001t0001g0198others(1): Show | 4 | HG01069.hp1 HG01358.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662-1808delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642429 | ||||||
chrX:123642447
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1662-1825A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642447 | ||||||
chrX:123642845
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 250 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1661+1730T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642845 | ||||||
chrX:123642883
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1661+1692A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123642883 | ||||||
chrX:123643220
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1661+1355G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643220 | ||||||
chrX:123643584
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1661+991A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643584 | ||||||
chrX:123643732
|
G | GA | 2 | a0001c0001t0001g0008a0001c0001t0001g0080 | 2 | HG02135.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1661+842dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643732 | ||||||
chrX:123643732
|
GA | G | 1 | a0001c0001t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1661+842delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123643732 | ||||||
chrX:123644490
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1661+85G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123644490 | ||||||
chrX:123644500
|
G | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1661+75C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 15/38 | chrX | 123644500 | ||||||
chrX:123645053
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1429-144C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 13/38 | chrX | 123645053 | ||||||
chrX:123645106
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1429-197C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 13/38 | chrX | 123645106 | ||||||
chrX:123645384
|
TA | T | 1 | a0001c0001t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1387-10delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645384 | ||||||
chrX:123645690
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1387-315C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645690 | ||||||
chrX:123645700
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0140a0001c0001t0001g0168others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-325C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645700 | ||||||
chrX:123645737
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1387-362T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645737 | ||||||
chrX:123645835
|
A | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-460T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645835 | ||||||
chrX:123645949
|
C | CA | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1387-575dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645949 | ||||||
chrX:123645949
|
C | CAA | 2 | a0001c0001t0001g0067a0001c0001t0001g0165 | 2 | HG02129.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1387-576_1387-575d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123645949 | ||||||
chrX:123646051
|
T | A | 1 | a0001c0001t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1387-676A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646051 | ||||||
chrX:123646265
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1387-890G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646265 | ||||||
chrX:123646460
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0055 | 2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1387-1085C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646460 | ||||||
chrX:123646532
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0093 | 3 | HG02622.hp1 HG03471.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1387-1157G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646532 | ||||||
chrX:123646686
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1387-1311A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123646686 | ||||||
chrX:123647056
|
T | G | 1 | a0001c0001t0001g0014 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1387-1681A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647056 | ||||||
chrX:123647356
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1387-1981C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647356 | ||||||
chrX:123647445
|
G | GCATT | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1387-2074_1387-207 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647445 | ||||||
chrX:123647522
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-2147T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647522 | ||||||
chrX:123647770
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-2395C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647770 | ||||||
chrX:123647771
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-2396C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647771 | ||||||
chrX:123647840
|
C | CA | 68 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0127others(65): Show | 68 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1387-2466dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | ||||||
chrX:123647840
|
C | CAA | 4 | a0001c0001t0001g0132a0001c0001t0001g0179a0001c0001t0001g0184others(1): Show | 4 | HG02056.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-2467_1387-246 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | ||||||
chrX:123647840
|
CA | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1387-2466delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | ||||||
chrX:123647840
|
CAA | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0094others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1387-2467_1387-246 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | ||||||
chrX:123647840
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-2478_1387-246 others(17): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647840 | ||||||
chrX:123647940
|
G | A | 11 | a0001c0001t0001g0132a0001c0001t0001g0184a0001c0001t0001g0185others(8): Show | 11 | HG01167.hp1 HG01952.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387-2565C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647940 | ||||||
chrX:123647986
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1387-2611G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123647986 | ||||||
chrX:123648280
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1387-2905A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648280 | ||||||
chrX:123648420
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1387-3045A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648420 | ||||||
chrX:123648456
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | NA18971.hp1 NA19007.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-3081C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648456 | ||||||
chrX:123648601
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0177 | 2 | NA18985.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1387-3226C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123648601 | ||||||
chrX:123649017
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-3642G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649017 | ||||||
chrX:123649081
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1387-3706C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649081 | ||||||
chrX:123649586
|
A | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1387-4211T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649586 | ||||||
chrX:123649974
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1387-4599A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123649974 | ||||||
chrX:123650101
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-4726G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650101 | ||||||
chrX:123650164
|
A | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-4789T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650164 | ||||||
chrX:123650170
|
AG | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG01358.hp1 HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1387-4796delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650170 | ||||||
chrX:123650661
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1387-5286A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650661 | ||||||
chrX:123650675
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0221 | 2 | NA18959.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1387-5300C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123650675 | ||||||
chrX:123651057
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(7): Show | 10 | HG01891.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1387-5682G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651057 | ||||||
chrX:123651126
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-5751T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651126 | ||||||
chrX:123651421
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1387-6046A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651421 | ||||||
chrX:123651539
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1387-6164A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651539 | ||||||
chrX:123651674
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1387-6299C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651674 | ||||||
chrX:123651708
|
A | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1387-6333T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651708 | ||||||
chrX:123651725
|
G | GC | 12 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0087others(9): Show | 12 | HG01081.hp2 HG01496.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1387-6351dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651725 | ||||||
chrX:123651725
|
G | GCC | 2 | a0001c0001t0001g0012a0001c0001t0001g0112 | 2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1387-6352_1387-635 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651725 | ||||||
chrX:123651725
|
GC | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0175 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1387-6351delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651725 | ||||||
chrX:123651727
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1387-6352G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651727 | ||||||
chrX:123651730
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-6355G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651730 | ||||||
chrX:123651731
|
C | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1387-6356G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651731 | ||||||
chrX:123651732
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1387-6357G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651732 | ||||||
chrX:123651733
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1387-6358G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123651733 | ||||||
chrX:123652013
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1387-6638A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652013 | ||||||
chrX:123652040
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-6665A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652040 | ||||||
chrX:123652104
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1387-6729G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652104 | ||||||
chrX:123652354
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387-6979G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652354 | ||||||
chrX:123652714
|
T | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0159others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-7339A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652714 | ||||||
chrX:123652761
|
A | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1387-7386T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652761 | ||||||
chrX:123652827
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1387-7452T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123652827 | ||||||
chrX:123653011
|
C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1387-7636G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653011 | ||||||
chrX:123653143
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1387-7768C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653143 | ||||||
chrX:123653296
|
G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-7921C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653296 | ||||||
chrX:123653573
|
G | GA | 1 | a0001c0002t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1387-8199dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653573 | ||||||
chrX:123653679
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1387-8304C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653679 | ||||||
chrX:123653968
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1387-8593G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123653968 | ||||||
chrX:123654186
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1387-8811C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654186 | ||||||
chrX:123654236
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1387-8861G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654236 | ||||||
chrX:123654313
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-8938C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654313 | ||||||
chrX:123654494
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1387-9119G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654494 | ||||||
chrX:123654627
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1387-9252G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654627 | ||||||
chrX:123654630
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387-9255C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654630 | ||||||
chrX:123654640
|
TC | T | 1 | a0001c0001t0001g0028 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1387-9266delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654640 | ||||||
chrX:123654758
|
C | CA | 76 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0053others(73): Show | 76 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.1387-9384dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
C | CAA | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0201others(3): Show | 6 | HG01516.hp1 HG02056.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-9385_1387-938 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
C | CAAA | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1387-9386_1387-938 others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
CA | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1387-9384delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
CAA | C | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-9385_1387-938 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
CAAAAA | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0225 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1387-9388_1387-938 others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123654758
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1387-9394_1387-938 others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123654758 | ||||||
chrX:123655026
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1387-9651C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655026 | ||||||
chrX:123655206
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0207 | 2 | HG01106.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1387-9831G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655206 | ||||||
chrX:123655292
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1387-9917A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655292 | ||||||
chrX:123655996
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1386+9646C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123655996 | ||||||
chrX:123656019
|
G | GA | 2 | a0001c0001t0001g0094a0001c0001t0001g0098 | 2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1386+9622dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656019 | ||||||
chrX:123656020
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1386+9622T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656020 | ||||||
chrX:123656051
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1386+9591C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656051 | ||||||
chrX:123656330
|
T | TA | 8 | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0139others(5): Show | 8 | HG00741.hp2 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+9311dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | ||||||
chrX:123656330
|
T | TAA | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1386+9310_1386+931 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | ||||||
chrX:123656330
|
TA | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG00323.hp1 HG00639.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1386+9311delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | ||||||
chrX:123656330
|
TAA | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0229 | 2 | HG01167.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1386+9310_1386+931 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656330 | ||||||
chrX:123656352
|
A | AAG | 3 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0086 | 3 | NA18994.hp1 NA19006.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1386+9288_1386+928 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656352 | ||||||
chrX:123656352
|
A | AG | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1386+9289_1386+929 others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656352 | ||||||
chrX:123656352
|
AAGAG | A | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1386+9286_1386+928 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656352 | ||||||
chrX:123656420
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1386+9222G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656420 | ||||||
chrX:123656462
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1386+9180T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656462 | ||||||
chrX:123656660
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1386+8982C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656660 | ||||||
chrX:123656723
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386+8919G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656723 | ||||||
chrX:123656813
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+8829A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656813 | ||||||
chrX:123656853
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0219a0001c0001t0001g0226 | 3 | HG00738.hp1 NA18952.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1386+8789A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656853 | ||||||
chrX:123656941
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1386+8701G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656941 | ||||||
chrX:123656946
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+8696C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123656946 | ||||||
chrX:123657029
|
A | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1386+8613T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657029 | ||||||
chrX:123657379
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0042 | 2 | HG02896.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1386+8263C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657379 | ||||||
chrX:123657431
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+8211T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657431 | ||||||
chrX:123657437
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1386+8205A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657437 | ||||||
chrX:123657437
|
TAAAC | T | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1386+8201_1386+820 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657437 | ||||||
chrX:123657513
|
GA | G | 1 | a0001c0001t0001g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1386+8128delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657513 | ||||||
chrX:123657644
|
T | TA | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1386+7997dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657644 | ||||||
chrX:123657891
|
CTAATA | C | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+7746_1386+775 others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657891 | ||||||
chrX:123657960
|
C | CGT | 2 | a0001c0001t0001g0165a0001c0001t0001g0167 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1386+7680_1386+768 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
C | CGTGT | 1 | a0001c0001t0001g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1386+7678_1386+768 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGT | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(65): Show | 68 | HG00621.hp1 HG00639.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.1386+7680_1386+768 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGTGT | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 65 | HG00438.hp1 HG00438.hp2 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.1386+7678_1386+768 others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGTGTGT | C | 73 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(70): Show | 73 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.1386+7676_1386+768 others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGTGTGTG others(1): Show |
C | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1386+7674_1386+768 others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1386+7672_1386+768 others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123657960
|
CGTGTGTG others(15): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+7660_1386+768 others(26): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123657960 | ||||||
chrX:123658175
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1386+7467G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658175 | ||||||
chrX:123658244
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1386+7398G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658244 | ||||||
chrX:123658568
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1386+7074T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658568 | ||||||
chrX:123658873
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1386+6769T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658873 | ||||||
chrX:123658896
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1386+6746C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123658896 | ||||||
chrX:123659142
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+6500G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659142 | ||||||
chrX:123659261
|
G | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0123a0001c0001t0001g0124others(7): Show | 10 | HG00323.hp2 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+6381C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659261 | ||||||
chrX:123659262
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1386+6380C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659262 | ||||||
chrX:123659311
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1386+6331C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659311 | ||||||
chrX:123659347
|
C | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1386+6295G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659347 | ||||||
chrX:123659447
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0183 | 3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1386+6195A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659447 | ||||||
chrX:123659502
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+6140G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659502 | ||||||
chrX:123659507
|
G | GT | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+6134dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659507 | ||||||
chrX:123659546
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1386+6096C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659546 | ||||||
chrX:123659556
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0159others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+6086G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659556 | ||||||
chrX:123659565
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+6077C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659565 | ||||||
chrX:123659663
|
A | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+5979T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123659663 | ||||||
chrX:123660110
|
AT | A | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1386+5531delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660110 | ||||||
chrX:123660111
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1386+5531A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660111 | ||||||
chrX:123660149
|
A | AG | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+5492dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660149 | ||||||
chrX:123660220
|
G | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1386+5422C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660220 | ||||||
chrX:123660301
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0104 | 2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1386+5341C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660301 | ||||||
chrX:123660656
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+4986G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660656 | ||||||
chrX:123660787
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1386+4855G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660787 | ||||||
chrX:123660950
|
G | GTA | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1386+4690_1386+469 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123660950 | ||||||
chrX:123661127
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1386+4515C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661127 | ||||||
chrX:123661273
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1386+4369G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661273 | ||||||
chrX:123661298
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1386+4344C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661298 | ||||||
chrX:123661360
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+4282C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661360 | ||||||
chrX:123661361
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0234a0001c0001t0001g0250 | 3 | HG01515.hp1 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1386+4281G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661361 | ||||||
chrX:123661404
|
T | TC | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+4237dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661404 | ||||||
chrX:123661439
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+4203G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661439 | ||||||
chrX:123661559
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1386+4083C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661559 | ||||||
chrX:123661597
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1386+4045G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661597 | ||||||
chrX:123661649
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1386+3993A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661649 | ||||||
chrX:123661718
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1386+3924A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661718 | ||||||
chrX:123661737
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1386+3905A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661737 | ||||||
chrX:123661753
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1386+3889C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123661753 | ||||||
chrX:123662079
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1386+3563A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662079 | ||||||
chrX:123662132
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1386+3510G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662132 | ||||||
chrX:123662312
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1386+3330G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662312 | ||||||
chrX:123662313
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1386+3329C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662313 | ||||||
chrX:123662368
|
C | T | 22 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0138others(19): Show | 22 | HG00438.hp2 HG01928.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1386+3274G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662368 | ||||||
chrX:123662402
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1386+3240G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662402 | ||||||
chrX:123662582
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1386+3060G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662582 | ||||||
chrX:123662587
|
C | CA | 17 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0137others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1386+3054dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662587 | ||||||
chrX:123662587
|
CA | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1386+3054delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662587 | ||||||
chrX:123662598
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1386+3044T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662598 | ||||||
chrX:123662661
|
TAAC | T | 1 | a0001c0001t0001g0215 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1386+2978_1386+298 others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123662661 | ||||||
chrX:123663531
|
A | AT | 8 | a0001c0001t0001g0092a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 8 | HG01243.hp1 HG01261.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+2110dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663531 | ||||||
chrX:123663538
|
T | TA | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1386+2103dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | ||||||
chrX:123663538
|
T | TAA | 32 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(29): Show | 32 | HG00621.hp1 HG01978.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.1386+2102_1386+210 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | ||||||
chrX:123663538
|
T | TTA | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1386+2103_1386+210 others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | ||||||
chrX:123663538
|
TA | T | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1386+2103delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663538 | ||||||
chrX:123663539
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+2103T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663539 | ||||||
chrX:123663622
|
TG | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1386+2019delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663622 | ||||||
chrX:123663623
|
G | GT | 3 | a0001c0001t0001g0053a0001c0001t0001g0112a0001c0005t0001g0111 | 3 | HG00741.hp2 HG01496.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1386+2018dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663623 | ||||||
chrX:123663623
|
G | GTTT | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1386+2016_1386+201 others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663623 | ||||||
chrX:123663784
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1386+1858G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663784 | ||||||
chrX:123663795
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+1847C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663795 | ||||||
chrX:123663807
|
T | TC | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+1834dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663807 | ||||||
chrX:123663847
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1386+1795T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123663847 | ||||||
chrX:123664111
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0247 | 3 | HG02630.hp2 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1386+1531A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664111 | ||||||
chrX:123664138
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1386+1504T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664138 | ||||||
chrX:123664245
|
T | TA | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1386+1396dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664245 | ||||||
chrX:123664837
|
ATGTTT | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1386+800_1386+804d others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123664837 | ||||||
chrX:123665125
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1386+517G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665125 | ||||||
chrX:123665299
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1386+343G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665299 | ||||||
chrX:123665513
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1386+129G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665513 | ||||||
chrX:123665576
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104 | 3 | HG00323.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1386+66T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 12/38 | chrX | 123665576 | ||||||
chrX:123665865
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1191-28T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665865 | ||||||
chrX:123665899
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1191-62A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665899 | ||||||
chrX:123665910
|
A | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0086 | 2 | NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1191-73T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665910 | ||||||
chrX:123665945
|
A | ATCAGTGA others(3): Show |
1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1191-118_1191-109d others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123665945 | ||||||
chrX:123666155
|
CTG | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1191-320_1191-319d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666155 | ||||||
chrX:123666200
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1191-363C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666200 | ||||||
chrX:123666351
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1191-514A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666351 | ||||||
chrX:123666633
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0081 | 2 | HG01934.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1190+473C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666633 | ||||||
chrX:123666746
|
A | G | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0091others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1190+360T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123666746 | ||||||
chrX:123667042
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1190+64A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 11/38 | chrX | 123667042 | ||||||
chrX:123667573
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1018-295T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 10/38 | chrX | 123667573 | ||||||
chrX:123667759
|
TA | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0076 | 2 | NA18747.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1017+399delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 10/38 | chrX | 123667759 | ||||||
chrX:123667888
|
A | G | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(1): Show | 4 | HG02015.hp1 HG02129.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+271T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 10/38 | chrX | 123667888 | ||||||
chrX:123669140
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0248 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.862-826T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669140 | ||||||
chrX:123669160
|
C | CA | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.862-847dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669160 | ||||||
chrX:123669244
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0053 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.862-930T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669244 | ||||||
chrX:123669323
|
C | CT | 4 | a0001c0001t0001g0051a0001c0001t0001g0115a0001c0001t0001g0248others(1): Show | 4 | HG02015.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-1010dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669323 | ||||||
chrX:123669323
|
CT | C | 1 | a0001c0001t0001g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.862-1010delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669323 | ||||||
chrX:123669861
|
CT | C | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.862-1548delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669861 | ||||||
chrX:123669902
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.862-1588A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669902 | ||||||
chrX:123669987
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.862-1673G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123669987 | ||||||
chrX:123670019
|
TATC | T | 2 | a0001c0001t0001g0146a0002c0006t0001g0147 | 2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.861+1647_861+1649d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670019 | ||||||
chrX:123670246
|
TC | T | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.861+1422delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670246 | ||||||
chrX:123670336
|
T | TG | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.861+1332dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670336 | ||||||
chrX:123670511
|
TG | T | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.861+1157delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670511 | ||||||
chrX:123670523
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861+1146C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670523 | ||||||
chrX:123670827
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.861+842A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670827 | ||||||
chrX:123670945
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.861+724G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123670945 | ||||||
chrX:123671173
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.861+496G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671173 | ||||||
chrX:123671305
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02135.hp1 NA18994.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.861+364A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671305 | ||||||
chrX:123671371
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.861+298A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671371 | ||||||
chrX:123671570
|
C | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 229 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.861+99G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671570 | ||||||
chrX:123671620
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.861+49A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 9/38 | chrX | 123671620 | ||||||
chrX:123672106
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0034others(6): Show | 9 | HG02135.hp1 HG02273.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-345C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672106 | ||||||
chrX:123672148
|
G | GT | 2 | a0001c0001t0001g0097a0001c0001t0001g0103 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.769-388dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672148 | ||||||
chrX:123672302
|
C | CT | 3 | a0001c0001t0001g0140a0001c0001t0001g0189a0001c0001t0001g0234 | 3 | HG01517.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769-542dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672302 | ||||||
chrX:123672302
|
CT | C | 1 | a0001c0001t0001g0052 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.769-542delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672302 | ||||||
chrX:123672807
|
A | ATAAC | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.769-1050_769-1047d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672807 | ||||||
chrX:123672980
|
T | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.769-1219A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123672980 | ||||||
chrX:123673150
|
A | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-1389T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673150 | ||||||
chrX:123673344
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.769-1583T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673344 | ||||||
chrX:123673761
|
C | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02809.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769-2000G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673761 | ||||||
chrX:123673879
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.769-2118G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123673879 | ||||||
chrX:123674092
|
G | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.769-2331C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674092 | ||||||
chrX:123674639
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.769-2878T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674639 | ||||||
chrX:123674647
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.769-2886G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674647 | ||||||
chrX:123674845
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.769-3084G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674845 | ||||||
chrX:123674962
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0183 | 3 | HG02818.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-3201T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123674962 | ||||||
chrX:123675019
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.769-3258T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675019 | ||||||
chrX:123675467
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.769-3706G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675467 | ||||||
chrX:123675596
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.769-3835A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675596 | ||||||
chrX:123675642
|
C | CA | 4 | a0001c0001t0001g0104a0001c0001t0001g0181a0001c0001t0001g0195others(1): Show | 4 | HG01433.hp1 HG02738.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-3882dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675642 | ||||||
chrX:123675642
|
CA | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.769-3882delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675642 | ||||||
chrX:123675652
|
C | CA | 1 | a0001c0001t0001g0054 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.769-3892dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675652 | ||||||
chrX:123675826
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.769-4065C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123675826 | ||||||
chrX:123676416
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.769-4655C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123676416 | ||||||
chrX:123676461
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.769-4700G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123676461 | ||||||
chrX:123677371
|
CATTAA | C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.769-5615_769-5611d others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677371 | ||||||
chrX:123677402
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.769-5641A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677402 | ||||||
chrX:123677443
|
CCTTAT | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0212 | 3 | NA18960.hp1 NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.769-5687_769-5683d others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677443 | ||||||
chrX:123677461
|
AT | A | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.769-5701delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677461 | ||||||
chrX:123677530
|
AAT | A | 1 | a0001c0001t0001g0217 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.769-5771_769-5770d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677530 | ||||||
chrX:123677871
|
C | CA | 48 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 48 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.769-6111dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677871 | ||||||
chrX:123677871
|
C | CAA | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.769-6112_769-6111d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677871 | ||||||
chrX:123677871
|
CAAAAAAA | C | 1 | a0001c0001t0001g0240 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.769-6117_769-6111d others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677871 | ||||||
chrX:123677986
|
G | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-6225C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123677986 | ||||||
chrX:123678199
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.769-6438G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678199 | ||||||
chrX:123678267
|
C | CT | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 45 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.769-6507dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678267 | ||||||
chrX:123678267
|
C | CTT | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.769-6508_769-6507d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678267 | ||||||
chrX:123678267
|
CT | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0148 | 2 | HG02109.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.769-6507delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678267 | ||||||
chrX:123678288
|
T | C | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.769-6527A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678288 | ||||||
chrX:123678308
|
C | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.769-6547G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678308 | ||||||
chrX:123678360
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.769-6599G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678360 | ||||||
chrX:123678432
|
A | AT | 1 | a0001c0001t0001g0029 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.769-6672dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678432 | ||||||
chrX:123678728
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.769-6967A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123678728 | ||||||
chrX:123679478
|
TA | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.768+7069delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679478 | ||||||
chrX:123679710
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.768+6838C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679710 | ||||||
chrX:123679713
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.768+6835C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679713 | ||||||
chrX:123679961
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+6587C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123679961 | ||||||
chrX:123680020
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02257.hp1 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.768+6528A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680020 | ||||||
chrX:123680061
|
G | GTCCCCCA others(11): Show |
1 | a0001c0001t0001g0018 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.768+6469_768+6486d others(20): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680061 | ||||||
chrX:123680094
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0175 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.768+6454G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680094 | ||||||
chrX:123680191
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768+6357G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680191 | ||||||
chrX:123680569
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.768+5979G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680569 | ||||||
chrX:123680579
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0034others(6): Show | 9 | HG02135.hp1 HG02273.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+5969G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680579 | ||||||
chrX:123680584
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.768+5964G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680584 | ||||||
chrX:123680965
|
T | TTCTC | 2 | a0001c0001t0001g0022a0001c0001t0001g0247 | 2 | HG01934.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.768+5579_768+5582d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680965 | ||||||
chrX:123680965
|
TTCTC | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+5579_768+5582d others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123680965 | ||||||
chrX:123681027
|
T | C | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.768+5521A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681027 | ||||||
chrX:123681374
|
T | TG | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0104others(3): Show | 6 | HG02071.hp1 HG02145.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+5173dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681374 | ||||||
chrX:123681591
|
G | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+4957C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681591 | ||||||
chrX:123681721
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.768+4827A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681721 | ||||||
chrX:123681974
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.768+4574C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123681974 | ||||||
chrX:123682487
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.768+4061G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682487 | ||||||
chrX:123682529
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.768+4019C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682529 | ||||||
chrX:123682838
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0159others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+3710G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123682838 | ||||||
chrX:123683020
|
T | TC | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.768+3527dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683020 | ||||||
chrX:123683035
|
C | G | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+3513G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683035 | ||||||
chrX:123683121
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+3427A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683121 | ||||||
chrX:123683294
|
G | GA | 1 | a0001c0001t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.768+3253dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683294 | ||||||
chrX:123683341
|
A | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.768+3207T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683341 | ||||||
chrX:123683584
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.768+2964A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683584 | ||||||
chrX:123683600
|
C | CT | 13 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0119others(10): Show | 13 | HG01106.hp1 HG02055.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.768+2947dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683600 | ||||||
chrX:123683600
|
CT | C | 1 | a0001c0001t0001g0049 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.768+2947delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683600 | ||||||
chrX:123683630
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.768+2918G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683630 | ||||||
chrX:123683667
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.768+2881G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683667 | ||||||
chrX:123683726
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.768+2822C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123683726 | ||||||
chrX:123684081
|
C | T | 8 | a0001c0001t0001g0132a0001c0001t0001g0184a0001c0001t0001g0185others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.768+2467G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684081 | ||||||
chrX:123684243
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.768+2305T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684243 | ||||||
chrX:123684393
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.768+2155C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684393 | ||||||
chrX:123684482
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.768+2066G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684482 | ||||||
chrX:123684550
|
A | AT | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.768+1997dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684550 | ||||||
chrX:123684675
|
A | C | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+1873T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684675 | ||||||
chrX:123684681
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.768+1867G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684681 | ||||||
chrX:123684694
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.768+1854C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684694 | ||||||
chrX:123684960
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.768+1588G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123684960 | ||||||
chrX:123685035
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1513A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685035 | ||||||
chrX:123685283
|
G | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1265C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685283 | ||||||
chrX:123685400
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.768+1148C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685400 | ||||||
chrX:123685697
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.768+851C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685697 | ||||||
chrX:123685799
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768+749A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685799 | ||||||
chrX:123685977
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.768+571G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685977 | ||||||
chrX:123685985
|
G | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.768+563C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685985 | ||||||
chrX:123685996
|
T | TA | 2 | a0001c0001t0001g0140a0001c0001t0001g0189 | 2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.768+551dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123685996 | ||||||
chrX:123686046
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG00673.hp1 HG02015.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.768+502T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123686046 | ||||||
chrX:123686106
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.768+442G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 8/38 | chrX | 123686106 | ||||||
chrX:123687103
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.602-389G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687103 | ||||||
chrX:123687211
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.602-497A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687211 | ||||||
chrX:123687659
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.602-945G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687659 | ||||||
chrX:123687805
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.602-1091C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123687805 | ||||||
chrX:123688090
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.602-1376G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688090 | ||||||
chrX:123688188
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-1474A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688188 | ||||||
chrX:123688397
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0085 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-1683A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688397 | ||||||
chrX:123688502
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.602-1788T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688502 | ||||||
chrX:123688721
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-2007A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688721 | ||||||
chrX:123688897
|
TCTC | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(7): Show | 10 | HG01891.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.602-2186_602-2184d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123688897 | ||||||
chrX:123689712
|
GC | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-2999delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123689712 | ||||||
chrX:123689744
|
GT | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-3031delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123689744 | ||||||
chrX:123690013
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0156 | 3 | HG01192.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.602-3299A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690013 | ||||||
chrX:123690212
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0194 | 3 | HG02486.hp1 HG02572.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.602-3498C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690212 | ||||||
chrX:123690231
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.602-3517C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690231 | ||||||
chrX:123690261
|
GA | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-3548delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690261 | ||||||
chrX:123690505
|
TC | T | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-3792delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690505 | ||||||
chrX:123690525
|
AACC | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-3814_602-3812d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690525 | ||||||
chrX:123690529
|
A | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-3815T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690529 | ||||||
chrX:123690563
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0055 | 2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.602-3849T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690563 | ||||||
chrX:123690950
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.602-4236C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690950 | ||||||
chrX:123690989
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.602-4275T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123690989 | ||||||
chrX:123691009
|
C | CG | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-4296dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691009 | ||||||
chrX:123691148
|
G | GT | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-4435dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691148 | ||||||
chrX:123691240
|
C | CA | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.602-4527dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691240 | ||||||
chrX:123691389
|
AG | A | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+4631delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691389 | ||||||
chrX:123691524
|
GT | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+4496delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691524 | ||||||
chrX:123691546
|
GT | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+4474delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123691546 | ||||||
chrX:123692294
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.601+3727A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692294 | ||||||
chrX:123692482
|
G | A | 14 | a0001c0001t0001g0127a0001c0001t0001g0191a0001c0001t0001g0192others(11): Show | 14 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.601+3539C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692482 | ||||||
chrX:123692494
|
C | CT | 12 | a0001c0001t0001g0001a0001c0001t0001g0139a0001c0001t0001g0152others(9): Show | 12 | HG00438.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+3526dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | ||||||
chrX:123692494
|
CT | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.601+3526delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | ||||||
chrX:123692494
|
CTT | C | 6 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0168others(3): Show | 6 | HG01168.hp1 HG01496.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+3525_601+3526d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | ||||||
chrX:123692494
|
CTTT | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0159others(1): Show | 4 | HG01099.hp1 HG01106.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+3524_601+3526d others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692494 | ||||||
chrX:123692571
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601+3450T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692571 | ||||||
chrX:123692606
|
A | AT | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+3414dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692606 | ||||||
chrX:123692620
|
GC | G | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+3400delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692620 | ||||||
chrX:123692739
|
T | C | 1 | a0005c0003t0001g0063 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.601+3282A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692739 | ||||||
chrX:123692784
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.601+3237G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692784 | ||||||
chrX:123692872
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+3149T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123692872 | ||||||
chrX:123693049
|
G | GAC | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+2971_601+2972i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693049 | ||||||
chrX:123693091
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+2930G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693091 | ||||||
chrX:123693095
|
T | TA | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+2925dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693095 | ||||||
chrX:123693196
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.601+2825G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693196 | ||||||
chrX:123693202
|
TA | T | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+2818delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693202 | ||||||
chrX:123693233
|
TG | T | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+2787delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693233 | ||||||
chrX:123693241
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+2780A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693241 | ||||||
chrX:123693270
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.601+2751G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693270 | ||||||
chrX:123693407
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2614C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693407 | ||||||
chrX:123693409
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2612T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693409 | ||||||
chrX:123693410
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.601+2611A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693410 | ||||||
chrX:123693415
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.601+2606T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693415 | ||||||
chrX:123693473
|
TA | T | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.601+2547delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693473 | ||||||
chrX:123693920
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.601+2101C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693920 | ||||||
chrX:123693922
|
C | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.601+2099G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123693922 | ||||||
chrX:123694140
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.601+1881C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694140 | ||||||
chrX:123694163
|
TA | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0243a0001c0005t0001g0111 | 3 | HG01496.hp1 HG02976.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.601+1857delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694163 | ||||||
chrX:123694175
|
AT | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+1845delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694175 | ||||||
chrX:123694338
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01099.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.601+1683C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694338 | ||||||
chrX:123694434
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+1587C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694434 | ||||||
chrX:123694606
|
T | TA | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.601+1414dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694606 | ||||||
chrX:123694620
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | HG02300.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.601+1401C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694620 | ||||||
chrX:123694620
|
GA | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0116others(70): Show | 73 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.601+1400delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694620 | ||||||
chrX:123694621
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | HG02300.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.601+1400T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123694621 | ||||||
chrX:123695993
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.601+28T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 7/38 | chrX | 123695993 | ||||||
chrX:123697459
|
T | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345+222A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 5/38 | chrX | 123697459 | ||||||
chrX:123697472
|
G | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345+209C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 5/38 | chrX | 123697472 | ||||||
chrX:123698089
|
T | TA | 2 | a0001c0001t0001g0120a0001c0001t0001g0159 | 2 | HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.275-339dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698089 | ||||||
chrX:123698089
|
T | TAA | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.275-340_275-339dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698089 | ||||||
chrX:123698089
|
TA | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0116a0001c0001t0001g0117others(9): Show | 12 | HG01081.hp2 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.275-339delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698089 | ||||||
chrX:123698089
|
TAA | T | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.275-340_275-339del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698089 | ||||||
chrX:123698230
|
C | CG | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.275-480dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698230 | ||||||
chrX:123698330
|
C | G | 1 | a0001c0001t0001g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.275-579G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698330 | ||||||
chrX:123698330
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0050others(4): Show | 7 | HG00673.hp1 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-579G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698330 | ||||||
chrX:123698362
|
G | A | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0040others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.275-611C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698362 | ||||||
chrX:123698407
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.275-656C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698407 | ||||||
chrX:123698412
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.275-661G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698412 | ||||||
chrX:123698445
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-694C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698445 | ||||||
chrX:123698457
|
C | CA | 14 | a0001c0001t0001g0035a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.275-707dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698457 | ||||||
chrX:123698457
|
CA | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0068others(2): Show | 5 | HG02602.hp1 HG02897.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-707delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698457 | ||||||
chrX:123698706
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0093 | 2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.275-955G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698706 | ||||||
chrX:123698874
|
C | CA | 2 | a0001c0001t0001g0181a0001c0005t0001g0111 | 2 | HG01496.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.275-1124dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698874 | ||||||
chrX:123698874
|
CA | C | 1 | a0001c0001t0001g0196 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.275-1124delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698874 | ||||||
chrX:123698909
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0080 | 2 | HG02148.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.275-1158T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698909 | ||||||
chrX:123698929
|
G | T | 3 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02809.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.275-1178C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123698929 | ||||||
chrX:123699036
|
G | GA | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.275-1286dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699036 | ||||||
chrX:123699215
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | NA18993.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.275-1464A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699215 | ||||||
chrX:123699387
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-1636T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699387 | ||||||
chrX:123699491
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.275-1740C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699491 | ||||||
chrX:123699507
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.275-1756G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699507 | ||||||
chrX:123699645
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.275-1894G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123699645 | ||||||
chrX:123700321
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.275-2570G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700321 | ||||||
chrX:123700411
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.275-2660C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700411 | ||||||
chrX:123700503
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-2752C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700503 | ||||||
chrX:123700522
|
C | CG | 6 | a0001c0001t0001g0086a0001c0001t0001g0107a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp1 HG01496.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-2772dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700522 | ||||||
chrX:123700538
|
A | AG | 1 | a0001c0001t0001g0145 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.275-2788dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700538 | ||||||
chrX:123700543
|
G | GGT | 1 | a0001c0001t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.275-2793_275-2792i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700543 | ||||||
chrX:123700544
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.275-2793A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | ||||||
chrX:123700544
|
T | TG | 44 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0030others(41): Show | 44 | HG00438.hp2 HG01074.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.275-2794dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | ||||||
chrX:123700544
|
T | TGG | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.275-2795_275-2794d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | ||||||
chrX:123700544
|
TG | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(74): Show | 77 | HG00280.hp1 HG00642.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.275-2794delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700544 | ||||||
chrX:123700551
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.275-2800C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700551 | ||||||
chrX:123700553
|
G | GGT | 14 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0136others(11): Show | 14 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.275-2803_275-2802i others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700553 | ||||||
chrX:123700553
|
G | T | 10 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0081others(7): Show | 10 | HG01243.hp1 HG02647.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.275-2802C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700553 | ||||||
chrX:123700554
|
T | G | 25 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0081others(22): Show | 25 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.275-2803A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700554 | ||||||
chrX:123700554
|
T | TG | 11 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0064others(8): Show | 11 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.275-2804dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700554 | ||||||
chrX:123700686
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.274+2768C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123700686 | ||||||
chrX:123701229
|
G | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+2225C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701229 | ||||||
chrX:123701692
|
C | CA | 30 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 30 | HG01099.hp1 HG01106.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.274+1761dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701692 | ||||||
chrX:123701692
|
C | CAA | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.274+1760_274+1761d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701692 | ||||||
chrX:123701692
|
CA | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0037 | 2 | HG02257.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.274+1761delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701692 | ||||||
chrX:123701711
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.274+1743A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701711 | ||||||
chrX:123701755
|
G | T | 1 | a0001c0001t0001g0213 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.274+1699C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123701755 | ||||||
chrX:123702775
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+679T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702775 | ||||||
chrX:123702816
|
G | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+638C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702816 | ||||||
chrX:123702849
|
G | GA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.274+604dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702849 | ||||||
chrX:123702928
|
C | CT | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.274+525dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123702928 | ||||||
chrX:123703094
|
T | TC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.274+359dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123703094 | ||||||
chrX:123703102
|
G | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0156 | 3 | HG01192.hp1 HG01346.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.274+352C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123703102 | ||||||
chrX:123703139
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.274+315G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 4/38 | chrX | 123703139 | ||||||
chrX:123703645
|
T | TG | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-141dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703645 | ||||||
chrX:123703673
|
A | AG | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-169dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703673 | ||||||
chrX:123703725
|
C | CA | 24 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0001t0001g0136others(21): Show | 24 | HG00438.hp2 HG01192.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.223-221dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
C | CAA | 2 | a0001c0001t0001g0154a0001c0001t0001g0199 | 2 | HG02083.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.223-222_223-221dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
C | CAAA | 1 | a0001c0001t0001g0207 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.223-223_223-221dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
CA | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 114 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.223-221delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
CAA | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0040others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.223-222_223-221del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
CAAAAAAA | C | 1 | a0001c0001t0001g0078 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.223-227_223-221del others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703725
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0021others(2): Show | 5 | HG02293.hp2 NA18942.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-228_223-221del others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703725 | ||||||
chrX:123703727
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-222T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703727 | ||||||
chrX:123703763
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.223-258C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703763 | ||||||
chrX:123703800
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-295T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703800 | ||||||
chrX:123703801
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-296C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703801 | ||||||
chrX:123703812
|
GC | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-308delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703812 | ||||||
chrX:123703890
|
T | TA | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.223-386dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(2): Show | 5 | HG01168.hp1 HG02683.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-392_223-386dup others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(1): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0146others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-393_223-386dup others(8): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(2): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(20): Show | 23 | HG01516.hp2 HG01891.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.223-394_223-386dup others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(3): Show |
44 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.223-395_223-386dup others(10): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(4): Show |
50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(47): Show | 50 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.223-396_223-386dup others(11): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(5): Show |
25 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0026others(22): Show | 25 | HG00735.hp1 HG01069.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-397_223-386dup others(12): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(6): Show |
10 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0001t0001g0119others(7): Show | 10 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-398_223-386dup others(13): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(7): Show |
4 | a0001c0001t0001g0118a0001c0001t0001g0162a0001c0001t0001g0168others(1): Show | 4 | HG02559.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-399_223-386dup others(14): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0249 | 2 | HG02055.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.223-400_223-386dup others(15): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0001g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-401_223-386dup others(16): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0001g0027 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.223-402_223-386dup others(17): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
TA | T | 58 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0127others(55): Show | 58 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.223-386delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
TAA | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0181a0001c0001t0001g0214others(3): Show | 6 | HG01515.hp1 HG02976.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-387_223-386del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
TAAAAAAA | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-392_223-386del others(7): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123703890
|
TAAAAAAA others(2): Show |
T | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.223-394_223-386del others(9): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123703890 | ||||||
chrX:123704107
|
T | TA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-603dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704107 | ||||||
chrX:123704133
|
TC | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.223-629delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704133 | ||||||
chrX:123704463
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0079 | 3 | HG00621.hp1 HG02027.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.223-958A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704463 | ||||||
chrX:123704598
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.223-1093C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704598 | ||||||
chrX:123704996
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.223-1491C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123704996 | ||||||
chrX:123705415
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.222+1443G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705415 | ||||||
chrX:123705544
|
TA | T | 1 | a0001c0001t0001g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.222+1313delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705544 | ||||||
chrX:123705820
|
T | TCA | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.222+1036_222+1037d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705820 | ||||||
chrX:123705879
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.222+979G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705879 | ||||||
chrX:123705918
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.222+940C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705918 | ||||||
chrX:123705939
|
T | C | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+919A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705939 | ||||||
chrX:123705981
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222+877C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123705981 | ||||||
chrX:123706095
|
CAAT | C | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.222+760_222+762del others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706095 | ||||||
chrX:123706098
|
TAA | T | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.222+758_222+759del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706098 | ||||||
chrX:123706357
|
G | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0239 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.222+501C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706357 | ||||||
chrX:123706373
|
CT | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(39): Show |
intron_variant | MODIFIER | c.222+484delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706373 | ||||||
chrX:123706424
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.222+434C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706424 | ||||||
chrX:123706514
|
T | TC | 5 | a0001c0001t0001g0044a0001c0001t0001g0065a0001c0001t0001g0117others(2): Show | 5 | HG02809.hp2 HG03225.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+343dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706514 | ||||||
chrX:123706721
|
T | TA | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.222+136dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 3/38 | chrX | 123706721 | ||||||
chrX:123707244
|
TTC | T | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.131-297_131-296del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707244 | ||||||
chrX:123707502
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.131-553A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707502 | ||||||
chrX:123707965
|
TA | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0181a0001c0001t0001g0191 | 3 | HG00280.hp1 HG01168.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.131-1017delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707965 | ||||||
chrX:123707991
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-1042T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123707991 | ||||||
chrX:123708107
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.131-1158A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708107 | ||||||
chrX:123708187
|
T | TC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.131-1239dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708187 | ||||||
chrX:123708187
|
TC | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.131-1239delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708187 | ||||||
chrX:123708528
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.131-1579C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708528 | ||||||
chrX:123708732
|
T | TC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.131-1784dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708732 | ||||||
chrX:123708772
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-1823T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708772 | ||||||
chrX:123708849
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.131-1900G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123708849 | ||||||
chrX:123709119
|
T | TC | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.131-2171_131-2170i others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709119 | ||||||
chrX:123709329
|
A | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-2380T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709329 | ||||||
chrX:123709398
|
T | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0151 | 2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.131-2449A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709398 | ||||||
chrX:123709460
|
G | A | 2 | a0001c0001t0001g0146a0002c0006t0001g0147 | 2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.131-2511C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709460 | ||||||
chrX:123709584
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.131-2635G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709584 | ||||||
chrX:123709693
|
C | T | 2 | a0001c0001t0001g0146a0002c0006t0001g0147 | 2 | HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.131-2744G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709693 | ||||||
chrX:123709923
|
T | TG | 1 | a0001c0001t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.130+2926dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123709923 | ||||||
chrX:123710173
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+2677T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710173 | ||||||
chrX:123710316
|
CAG | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+2532_130+2533d others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710316 | ||||||
chrX:123710611
|
TG | T | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+2238delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710611 | ||||||
chrX:123710758
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.130+2092C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123710758 | ||||||
chrX:123711009
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+1841G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711009 | ||||||
chrX:123711188
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+1662A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711188 | ||||||
chrX:123711194
|
TG | T | 1 | a0001c0001t0001g0017 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.130+1655delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711194 | ||||||
chrX:123711195
|
G | GT | 14 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0019others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+1654dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711195 | ||||||
chrX:123711200
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+1650A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711200 | ||||||
chrX:123711201
|
G | GT | 1 | a0001c0001t0001g0213 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.130+1648dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711201 | ||||||
chrX:123711201
|
G | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.130+1649C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711201 | ||||||
chrX:123711237
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+1613T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711237 | ||||||
chrX:123711238
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130+1612C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711238 | ||||||
chrX:123711479
|
C | CA | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.130+1370dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711479 | ||||||
chrX:123711613
|
G | A | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+1237C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711613 | ||||||
chrX:123711679
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.130+1171T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711679 | ||||||
chrX:123711767
|
G | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0089 | 2 | NA18612.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.130+1083C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711767 | ||||||
chrX:123711779
|
A | G | 2 | a0001c0001t0001g0152a0001c0002t0001g0153 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.130+1071T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711779 | ||||||
chrX:123711878
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.130+972C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711878 | ||||||
chrX:123711958
|
T | TA | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 181 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.130+891dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | ||||||
chrX:123711958
|
T | TAA | 43 | a0001c0001t0001g0013a0001c0001t0001g0059a0001c0001t0001g0081others(40): Show | 43 | HG00673.hp1 HG00738.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.130+890_130+891dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | ||||||
chrX:123711958
|
T | TAAA | 4 | a0001c0001t0001g0122a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG00741.hp1 HG01168.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+889_130+891dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | ||||||
chrX:123711958
|
TA | T | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.130+891delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | ||||||
chrX:123711958
|
TAAAAA | T | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.130+887_130+891del others(5): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123711958 | ||||||
chrX:123712030
|
A | AAT | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+818_130+819dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712030 | ||||||
chrX:123712136
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG01192.hp1 HG01346.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+714C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712136 | ||||||
chrX:123712198
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130+652G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712198 | ||||||
chrX:123712229
|
C | T | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+621G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712229 | ||||||
chrX:123712794
|
GCAGA | G | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.130+52_130+55delTC others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712794 | ||||||
chrX:123712831
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+19T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 2/38 | chrX | 123712831 | ||||||
chrX:123713000
|
A | C | 2 | a0001c0001t0001g0112a0001c0005t0001g0111 | 2 | HG01496.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.72-92T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713000 | ||||||
chrX:123713251
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-343A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713251 | ||||||
chrX:123713283
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-375C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713283 | ||||||
chrX:123713411
|
G | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.72-503C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713411 | ||||||
chrX:123713432
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-524C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713432 | ||||||
chrX:123713476
|
C | CA | 16 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0001g0080others(13): Show | 16 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-569dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713476 | ||||||
chrX:123713476
|
C | CAAAAAAA others(1): Show |
1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-576_72-569dupTT others(6): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713476 | ||||||
chrX:123713563
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0151 | 2 | HG00639.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72-655A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713563 | ||||||
chrX:123713754
|
G | GA | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-847dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713754 | ||||||
chrX:123713841
|
G | GA | 10 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0120others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-934dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713841 | ||||||
chrX:123713841
|
GA | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0179a0001c0001t0001g0224others(1): Show | 4 | HG02056.hp1 HG02109.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-934delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713841 | ||||||
chrX:123713898
|
TA | T | 1 | a0001c0001t0001g0130 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.72-991delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123713898 | ||||||
chrX:123714206
|
G | GTAA | 7 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | NA18945.hp1 NA18970.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-1301_72-1299dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714206 | ||||||
chrX:123714268
|
A | AT | 1 | a0001c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.72-1361dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714268 | ||||||
chrX:123714597
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0248 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-1689C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714597 | ||||||
chrX:123714693
|
A | AC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-1786dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123714693 | ||||||
chrX:123715019
|
C | CT | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.72-2112dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | ||||||
chrX:123715019
|
C | CTT | 59 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00438.hp2 HG00621.hp1 HG01934.hp1 others(56): Show |
intron_variant | MODIFIER | c.72-2113_72-2112dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | ||||||
chrX:123715019
|
C | CTTT | 4 | a0001c0001t0001g0014a0001c0001t0001g0122a0001c0001t0001g0174others(1): Show | 4 | HG01891.hp2 HG02055.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2114_72-2112dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | ||||||
chrX:123715019
|
CT | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0128a0001c0001t0001g0137others(5): Show | 8 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-2112delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715019 | ||||||
chrX:123715760
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-2852C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715760 | ||||||
chrX:123715784
|
C | CA | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(44): Show | 47 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.72-2877dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715784 | ||||||
chrX:123715784
|
CA | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0242 | 2 | HG03710.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.72-2877delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715784 | ||||||
chrX:123715836
|
GT | G | 1 | a0001c0001t0001g0008 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.72-2929delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715836 | ||||||
chrX:123715844
|
TA | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-2937delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715844 | ||||||
chrX:123715924
|
A | G | 10 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0118others(7): Show | 10 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-3016T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123715924 | ||||||
chrX:123716277
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-3369G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716277 | ||||||
chrX:123716375
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3467A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716375 | ||||||
chrX:123716453
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.72-3545G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716453 | ||||||
chrX:123716590
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0225 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.72-3682C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716590 | ||||||
chrX:123716728
|
C | CA | 7 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0081others(4): Show | 7 | HG02630.hp2 HG02717.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-3821dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716728 | ||||||
chrX:123716728
|
CA | C | 12 | a0001c0001t0001g0075a0001c0001t0001g0117a0001c0001t0001g0118others(9): Show | 12 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-3821delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716728 | ||||||
chrX:123716748
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-3840T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716748 | ||||||
chrX:123716825
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01256.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.72-3917C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123716825 | ||||||
chrX:123717001
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.72-4093A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717001 | ||||||
chrX:123717097
|
TG | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-4190delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717097 | ||||||
chrX:123717173
|
AT | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-4266delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717173 | ||||||
chrX:123717238
|
CA | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-4331delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717238 | ||||||
chrX:123717272
|
AG | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-4365delC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717272 | ||||||
chrX:123717344
|
C | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.72-4436G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717344 | ||||||
chrX:123717429
|
A | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-4521T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717429 | ||||||
chrX:123717463
|
AT | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-4556delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717463 | ||||||
chrX:123717693
|
C | CA | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 236 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.72-4786dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717693 | ||||||
chrX:123717693
|
C | CAA | 8 | a0001c0001t0001g0029a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG01261.hp1 HG02738.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-4787_72-4786dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717693 | ||||||
chrX:123717728
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01167.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72-4820G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717728 | ||||||
chrX:123717892
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.72-4984G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123717892 | ||||||
chrX:123718000
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0139 | 2 | HG02109.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.72-5092C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718000 | ||||||
chrX:123718262
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.72-5354G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718262 | ||||||
chrX:123718288
|
A | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.72-5380T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718288 | ||||||
chrX:123718292
|
CA | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-5385delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718292 | ||||||
chrX:123718388
|
A | AT | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-5481dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718388 | ||||||
chrX:123718427
|
C | CA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-5520dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718427 | ||||||
chrX:123718481
|
C | CG | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-5574dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718481 | ||||||
chrX:123718500
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.72-5592G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718500 | ||||||
chrX:123718615
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0182 | 2 | HG01168.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.72-5707G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718615 | ||||||
chrX:123718669
|
G | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.72-5761C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718669 | ||||||
chrX:123718758
|
CA | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0177 | 2 | HG02897.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.72-5851delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718758 | ||||||
chrX:123718816
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72-5908G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123718816 | ||||||
chrX:123719056
|
T | TA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6149dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719056 | ||||||
chrX:123719126
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-6218T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719126 | ||||||
chrX:123719172
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.72-6264G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719172 | ||||||
chrX:123719179
|
C | CA | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0139others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-6272dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719179 | ||||||
chrX:123719179
|
CA | C | 1 | a0001c0001t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72-6272delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719179 | ||||||
chrX:123719253
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-6345T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719253 | ||||||
chrX:123719275
|
G | GA | 1 | a0001c0001t0001g0081 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72-6368dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719275 | ||||||
chrX:123719297
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72-6389A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719297 | ||||||
chrX:123719366
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-6458A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719366 | ||||||
chrX:123719500
|
GC | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6593delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719500 | ||||||
chrX:123719580
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-6672C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719580 | ||||||
chrX:123719596
|
CA | C | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.72-6689delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719596 | ||||||
chrX:123719635
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6727A>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719635 | ||||||
chrX:123719636
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6728T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719636 | ||||||
chrX:123719655
|
A | AGCAG | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6748_72-6747ins others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719655 | ||||||
chrX:123719662
|
CA | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6755delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719662 | ||||||
chrX:123719672
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.72-6764G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719672 | ||||||
chrX:123719704
|
A | AG | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6797dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719704 | ||||||
chrX:123719770
|
C | CA | 8 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(5): Show | 8 | HG01891.hp1 NA18971.hp1 NA19007.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-6863dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719770 | ||||||
chrX:123719770
|
CA | C | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6863delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719770 | ||||||
chrX:123719773
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72-6865T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719773 | ||||||
chrX:123719783
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.72-6875T>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719783 | ||||||
chrX:123719824
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0247 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.72-6916C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719824 | ||||||
chrX:123719900
|
G | GC | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-6993dupG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123719900 | ||||||
chrX:123720004
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0167 | 2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72-7096G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720004 | ||||||
chrX:123720320
|
TC | T | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-7413delG | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720320 | ||||||
chrX:123720389
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72-7481C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720389 | ||||||
chrX:123720429
|
C | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(37): Show | 40 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.72-7521G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720429 | ||||||
chrX:123720637
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG00621.hp1 HG01934.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-7729T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720637 | ||||||
chrX:123720671
|
C | CA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-7764dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720671 | ||||||
chrX:123720825
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.72-7917G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720825 | ||||||
chrX:123720892
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-7984A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123720892 | ||||||
chrX:123721015
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01167.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72-8107A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721015 | ||||||
chrX:123721064
|
G | GT | 2 | a0001c0001t0001g0012a0001c0001t0001g0177 | 2 | HG03927.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.72-8157dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721064 | ||||||
chrX:123721147
|
G | GT | 11 | a0001c0001t0001g0113a0001c0001t0001g0123a0001c0001t0001g0124others(8): Show | 11 | HG00323.hp2 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-8240dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721147 | ||||||
chrX:123721147
|
GT | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-8240delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721147 | ||||||
chrX:123721165
|
G | GT | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72-8258dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721165 | ||||||
chrX:123721509
|
C | CG | 10 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0118others(7): Show | 10 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-8602dupC | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721509 | ||||||
chrX:123721701
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.72-8793C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721701 | ||||||
chrX:123721786
|
C | CA | 2 | a0001c0001t0001g0091a0001c0001t0001g0093 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.72-8879dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721786 | ||||||
chrX:123721786
|
CA | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0245 | 2 | HG01167.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72-8879delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721786 | ||||||
chrX:123721936
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.72-9028A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721936 | ||||||
chrX:123721955
|
GT | G | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-9048delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123721955 | ||||||
chrX:123722047
|
C | CA | 1 | a0001c0001t0001g0177 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72-9140dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722047 | ||||||
chrX:123722100
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9192G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722100 | ||||||
chrX:123722504
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.72-9596A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722504 | ||||||
chrX:123722632
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9724G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722632 | ||||||
chrX:123722732
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72-9824T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123722732 | ||||||
chrX:123723189
|
C | CA | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01167.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.71+9762dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723189 | ||||||
chrX:123723370
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(6): Show | 9 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+9582G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723370 | ||||||
chrX:123723411
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+9541C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723411 | ||||||
chrX:123723519
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+9433G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723519 | ||||||
chrX:123723602
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71+9350A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723602 | ||||||
chrX:123723690
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+9262T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723690 | ||||||
chrX:123723822
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.71+9130C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723822 | ||||||
chrX:123723903
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71+9049G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723903 | ||||||
chrX:123723904
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 238 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.71+9048T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123723904 | ||||||
chrX:123724272
|
T | C | 1 | a0001c0005t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.71+8680A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724272 | ||||||
chrX:123724295
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71+8657C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724295 | ||||||
chrX:123724346
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.71+8606T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724346 | ||||||
chrX:123724634
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+8318T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724634 | ||||||
chrX:123724973
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.71+7979C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724973 | ||||||
chrX:123724995
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71+7957G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123724995 | ||||||
chrX:123725157
|
T | TA | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.71+7794dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725157 | ||||||
chrX:123725297
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+7655C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725297 | ||||||
chrX:123725352
|
AGT | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+7598_71+7599del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725352 | ||||||
chrX:123725428
|
C | CA | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+7523dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725428 | ||||||
chrX:123725428
|
C | CAA | 5 | a0001c0001t0001g0075a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG01168.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+7522_71+7523dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725428 | ||||||
chrX:123725428
|
CA | C | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71+7523delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725428 | ||||||
chrX:123725616
|
C | CA | 41 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(38): Show | 41 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.71+7335dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | ||||||
chrX:123725616
|
C | CAA | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.71+7334_71+7335dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | ||||||
chrX:123725616
|
C | CAAA | 24 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0077others(21): Show | 24 | HG00621.hp1 HG01978.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.71+7333_71+7335dup others(3): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | ||||||
chrX:123725616
|
CA | C | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.71+7335delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725616 | ||||||
chrX:123725639
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71+7313G>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725639 | ||||||
chrX:123725735
|
C | T | 11 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(8): Show | 11 | HG01099.hp1 HG01106.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+7217G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725735 | ||||||
chrX:123725882
|
C | CA | 1 | a0001c0001t0001g0181 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.71+7069dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725882 | ||||||
chrX:123725896
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02818.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.71+7056C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123725896 | ||||||
chrX:123726512
|
C | CA | 9 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 9 | HG01175.hp1 HG01192.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+6439dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123726512 | ||||||
chrX:123726512
|
C | CAA | 1 | a0001c0001t0001g0182 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.71+6438_71+6439dup others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123726512 | ||||||
chrX:123726512
|
CA | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0196a0001c0001t0001g0246others(1): Show | 4 | HG02630.hp2 HG02717.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+6439delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123726512 | ||||||
chrX:123727220
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71+5732T>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727220 | ||||||
chrX:123727245
|
TA | T | 1 | a0001c0001t0001g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.71+5706delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727245 | ||||||
chrX:123727316
|
G | GTAGA | 1 | a0001c0001t0001g0105 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.71+5632_71+5635dup others(4): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727316 | ||||||
chrX:123727412
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71+5540G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727412 | ||||||
chrX:123727650
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71+5302G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727650 | ||||||
chrX:123727651
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71+5301C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727651 | ||||||
chrX:123727707
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.71+5245C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727707 | ||||||
chrX:123727853
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.71+5099C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123727853 | ||||||
chrX:123728053
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.71+4899C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728053 | ||||||
chrX:123728137
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.71+4815A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728137 | ||||||
chrX:123728205
|
G | GA | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.71+4746dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728205 | ||||||
chrX:123728242
|
T | TA | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.71+4709dupT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728242 | ||||||
chrX:123728242
|
TA | T | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.71+4709delT | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728242 | ||||||
chrX:123728339
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01168.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.71+4613G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728339 | ||||||
chrX:123728785
|
A | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+4167T>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728785 | ||||||
chrX:123728811
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.71+4141A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123728811 | ||||||
chrX:123729193
|
C | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.71+3759G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123729193 | ||||||
chrX:123729344
|
T | TG | 1 | a0001c0001t0001g0243 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.71+3607_71+3608ins others(1): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123729344 | ||||||
chrX:123729651
|
AAG | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 14 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+3299_71+3300del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123729651 | ||||||
chrX:123730068
|
G | C | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+2884C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730068 | ||||||
chrX:123730182
|
G | GT | 9 | a0001c0001t0001g0112a0001c0001t0001g0165a0001c0001t0001g0166others(6): Show | 9 | HG01496.hp1 HG02056.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+2769dupA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730182 | ||||||
chrX:123730182
|
GT | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.71+2769delA | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730182 | ||||||
chrX:123730182
|
GTT | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0245 | 2 | HG02976.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.71+2768_71+2769del others(2): Show |
THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730182 | ||||||
chrX:123730248
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.71+2704G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730248 | ||||||
chrX:123730397
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71+2555C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730397 | ||||||
chrX:123730851
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.71+2101C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123730851 | ||||||
chrX:123731135
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.71+1817G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731135 | ||||||
chrX:123731189
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.71+1763G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731189 | ||||||
chrX:123731671
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+1281A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123731671 | ||||||
chrX:123732007
|
T | G | 11 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(8): Show | 11 | HG02622.hp2 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+945A>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732007 | ||||||
chrX:123732144
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.71+808G>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732144 | ||||||
chrX:123732391
|
G | C | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(75): Show | 78 | HG00438.hp2 HG00741.hp1 HG01167.hp1 others(75): Show |
intron_variant | MODIFIER | c.71+561C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732391 | ||||||
chrX:123732461
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71+491C>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732461 | ||||||
chrX:123732462
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71+490C>A | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732462 | ||||||
chrX:123732586
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.71+366A>G | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732586 | ||||||
chrX:123732817
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.71+135C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732817 | ||||||
chrX:123732853
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.71+99C>T | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732853 | ||||||
chrX:123732941
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71+11G>C | THOC2 | ENSG00000125676.20 | transcript | ENST00000245838.13 | protein_coding | 1/38 | chrX | 123732941 |