geneid | 9984 |
---|---|
ensemblid | ENSG00000079134.13 |
hgncid | 19070 |
symbol | THOC1 |
name | THO complex subunit 1 |
refseq_nuc | NM_005131.3 |
refseq_prot | NP_005122.2 |
ensembl_nuc | ENST00000261600.11 |
ensembl_prot | ENSP00000261600.6 |
mane_status | MANE Select |
chr | chr18 |
start | 214520 |
end | 268047 |
strand | - |
ver | v1.2 |
region | chr18:214520-268047 |
region5000 | chr18:209520-273047 |
regionname0 | THOC1_chr18_214520_268047 |
regionname5000 | THOC1_chr18_209520_273047 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 657 | 376 | 94 | 68 | 156 | 14 | 42 | 120 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1974 | 293 | 73 | 60 | 104 | 14 | 41 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0002 | 0/0 | 1974 | 55 | 0 | 5 | 50 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0003 | 1/0 | 1974 | 24 | 21 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0004 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0005 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0006 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
c0007 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0006 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0010 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0033 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1974 | 293 | 73 | 60 | 104 | 14 | 41 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0002 | 0/0 | 1974 | 55 | 0 | 5 | 50 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0003 | 1/0 | 1974 | 24 | 21 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0004 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0005 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0006 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0007 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2108 | 277 | 73 | 54 | 104 | 11 | 34 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0001t0002 | 0/0 | 2111 | 16 | 0 | 6 | 0 | 3 | 7 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0002t0001 | 0/0 | 2108 | 55 | 0 | 5 | 50 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0003t0001 | 1/0 | 2108 | 24 | 21 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0004t0001 | 0/0 | 2108 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0005t0002 | 0/0 | 2111 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0006t0001 | 0/0 | 2108 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
a0001c0007t0001 | 0/0 | 2108 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | copy fasta | chr18 | 209520 | 273047 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0033 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0005t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0006t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
a0001c0007t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0268 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0269 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01358 | hp1 | a0001 | c0005 | t0002 | g0048 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0273 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0259 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0275 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0281 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | ESN | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0280 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | STU | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | CHB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18959 | hp2 | a0001 | c0007 | t0001 | g0115 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18984 | hp2 | a0001 | c0006 | t0001 | g0195 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0277 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0276 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0301 | AFR | LWK | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0272 | REF | REF | THOC1_chr18_209520_273047 | THOC1 | chr18 | 209520 | 273047 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:214842
|
C | T | 1 | a0001c0006 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1758G>A | p.Lys586Lys | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 21/21 | 1786/2108 | 1758/1974 | 586/657 | chr18 | 214842 | ||
chr18:224131
|
G | A | 2 | a0001c0002a0001c0006 | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
synonymous_variant | LOW | c.1257C>T | p.Pro419Pro | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/21 | 1285/2108 | 1257/1974 | 419/657 | chr18 | 224131 | ||
chr18:225116
|
A | G | 1 | a0001c0005 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1110T>C | p.Asp370Asp | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/21 | 1138/2108 | 1110/1974 | 370/657 | chr18 | 225116 | ||
chr18:226830
|
T | C | 1 | a0001c0007 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.990A>G | p.Gln330Gln | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/21 | 1018/2108 | 990/1974 | 330/657 | chr18 | 226830 | ||
chr18:252559
|
G | A | 6 | a0001c0001a0001c0002a0001c0004others(3): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
synonymous_variant | LOW | c.657C>T | p.Asp219Asp | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/21 | 685/2108 | 657/1974 | 219/657 | chr18 | 252559 | ||
chr18:254315
|
A | T | 1 | a0001c0004 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.561T>A | p.Thr187Thr | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/21 | 589/2108 | 561/1974 | 187/657 | chr18 | 254315 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:214930
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1679-9A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214930 | ||||||
chr18:214950
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1679-29G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214950 | ||||||
chr18:214951
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-30C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214951 | ||||||
chr18:214959
|
A | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(30): Show | 40 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1679-38T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214959 | ||||||
chr18:214983
|
T | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1679-62A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214983 | ||||||
chr18:214991
|
C | T | 49 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1679-70G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 214991 | ||||||
chr18:215020
|
A | G | 1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1679-99T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215020 | ||||||
chr18:215060
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0172a0001c0002t0001g0177 | 4 | NA18947.hp1 NA18968.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-139C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215060 | ||||||
chr18:215156
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1679-235G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215156 | ||||||
chr18:215299
|
A | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0039others(29): Show | 37 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1678+130T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215299 | ||||||
chr18:215345
|
G | C | 48 | a0001c0001t0001g0201a0001c0002t0001g0007a0001c0002t0001g0025others(45): Show | 57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1678+84C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215345 | ||||||
chr18:215384
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1678+45T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 20/20 | chr18 | 215384 | ||||||
chr18:215732
|
C | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0105 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1603-228G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215732 | ||||||
chr18:215808
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603-304G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215808 | ||||||
chr18:215966
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-463_1603-462i others(29): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215966 | ||||||
chr18:215974
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(52): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1603-470T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215974 | ||||||
chr18:215985
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-481A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215985 | ||||||
chr18:215993
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-489A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 215993 | ||||||
chr18:216023
|
G | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602+463C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216023 | ||||||
chr18:216142
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1602+344G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216142 | ||||||
chr18:216291
|
T | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0155 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1602+195A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216291 | ||||||
chr18:216332
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1602+154T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216332 | ||||||
chr18:216434
|
T | G | 1 | a0001c0002t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1602+52A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 19/20 | chr18 | 216434 | ||||||
chr18:216869
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1455-237dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 216869 | ||||||
chr18:216958
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1455-325G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 216958 | ||||||
chr18:217041
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1455-408A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217041 | ||||||
chr18:217049
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1455-416C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217049 | ||||||
chr18:217069
|
G | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455-436C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217069 | ||||||
chr18:217085
|
T | C | 1 | a0001c0002t0001g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1455-452A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217085 | ||||||
chr18:217171
|
C | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0134 | 2 | HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1455-538G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217171 | ||||||
chr18:217379
|
G | A | 20 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(17): Show | 24 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1455-746C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217379 | ||||||
chr18:217485
|
C | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0157others(1): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1455-852G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217485 | ||||||
chr18:217488
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1455-855C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217488 | ||||||
chr18:217494
|
T | C | 3 | a0001c0001t0001g0290a0001c0001t0001g0296a0001c0001t0001g0298 | 3 | HG00741.hp1 HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1455-861A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217494 | ||||||
chr18:217593
|
T | TG | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-961dupC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217593 | ||||||
chr18:217673
|
ACCTTCTC others(22): Show |
A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1455-1069_1455-104 others(33): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217673 | ||||||
chr18:217866
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 29 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1454+1020C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217866 | ||||||
chr18:217952
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1454+934C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 217952 | ||||||
chr18:218042
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1454+844T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218042 | ||||||
chr18:218226
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1454+660C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218226 | ||||||
chr18:218242
|
A | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+644T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218242 | ||||||
chr18:218285
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+601T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218285 | ||||||
chr18:218366
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1454+520G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218366 | ||||||
chr18:218418
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1454+468A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218418 | ||||||
chr18:218695
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(198): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1454+191A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218695 | ||||||
chr18:218753
|
C | A | 46 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(43): Show | 55 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1454+133G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 18/20 | chr18 | 218753 | ||||||
chr18:218980
|
CA | C | 7 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1371-12delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 218980 | ||||||
chr18:218980
|
CAAAAATA others(90): Show |
C | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1371-108_1371-12de others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 218980 | ||||||
chr18:219008
|
T | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0121others(6): Show | 9 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1371-39A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219008 | ||||||
chr18:219008
|
TTCTTAAT others(89): Show |
T | 1 | a0001c0001t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1371-135_1371-40de others(97): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219008 | ||||||
chr18:219029
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(185): Show | 229 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1371-60C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219029 | ||||||
chr18:219072
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 228 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1371-103T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219072 | ||||||
chr18:219076
|
CA | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0074others(7): Show | 11 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1371-108delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219076 | ||||||
chr18:219077
|
A | AAAAATAA others(88): Show |
1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1371-109_1371-108i others(97): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | ||||||
chr18:219077
|
A | AAAAATAA others(183): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0157others(1): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1371-109_1371-108i others(192): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | ||||||
chr18:219077
|
AAAAATAA others(183): Show |
A | 1 | a0001c0001t0001g0034 | 2 | NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1371-298_1371-109d others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219077 | ||||||
chr18:219172
|
C | CA | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0060others(12): Show | 17 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1371-204dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAAATA others(185): Show |
1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1371-204_1371-203i others(194): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(184): Show |
1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(89): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0001t0001g0092others(4): Show | 8 | HG00438.hp2 HG02027.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1371-299_1371-204d others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(184): Show |
265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1371-394_1371-204d others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(470): Show |
1 | a0001c0001t0001g0094 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(479): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(565): Show |
1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1371-204_1371-203i others(574): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219172
|
C | CAAAATAA others(184): Show |
1 | a0001c0001t0001g0221 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1371-204_1371-203i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219172 | ||||||
chr18:219190
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1371-221A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219190 | ||||||
chr18:219242
|
G | GTGGGCAT others(184): Show |
6 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0198others(3): Show | 7 | HG02109.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1371-274_1371-273i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219242 | ||||||
chr18:219242
|
G | GTGGGCAT others(184): Show |
1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1371-274_1371-273i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219242 | ||||||
chr18:219265
|
T | TACAAAAA others(89): Show |
1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1371-297_1371-296i others(98): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219265 | ||||||
chr18:219265
|
T | TACAAAAT others(184): Show |
2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1371-297_1371-296i others(193): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219265 | ||||||
chr18:219267
|
C | CA | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0130 | 3 | HG01168.hp2 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1371-299dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219267 | ||||||
chr18:219294
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-325G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219294 | ||||||
chr18:219452
|
C | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 8 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1371-483G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219452 | ||||||
chr18:219457
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1371-488G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 219457 | ||||||
chr18:220071
|
T | C | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1371-1102A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220071 | ||||||
chr18:220084
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1115G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220084 | ||||||
chr18:220226
|
G | A | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1371-1257C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220226 | ||||||
chr18:220341
|
C | A | 98 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(95): Show | 115 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.1371-1372G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220341 | ||||||
chr18:220441
|
AAC | A | 48 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1371-1474_1371-147 others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220441 | ||||||
chr18:220458
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1489G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220458 | ||||||
chr18:220658
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1371-1689C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220658 | ||||||
chr18:220706
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1371-1737T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220706 | ||||||
chr18:220757
|
T | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0183 | 3 | HG02015.hp2 HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1371-1788A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220757 | ||||||
chr18:220903
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1371-1934G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 220903 | ||||||
chr18:221102
|
G | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0039others(29): Show | 37 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1371-2133C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221102 | ||||||
chr18:221131
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1371-2162C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221131 | ||||||
chr18:221145
|
T | G | 1 | a0001c0001t0001g0289 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1371-2176A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221145 | ||||||
chr18:221175
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1371-2206A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221175 | ||||||
chr18:221228
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+2212T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221228 | ||||||
chr18:221350
|
A | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0138 | 2 | HG01109.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1370+2090T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221350 | ||||||
chr18:221410
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1370+2030A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221410 | ||||||
chr18:221606
|
C | CT | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(96): Show | 123 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1370+1833dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | ||||||
chr18:221606
|
C | CTT | 6 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0093others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370+1832_1370+183 others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | ||||||
chr18:221606
|
CT | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0043others(54): Show | 68 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1370+1833delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221606 | ||||||
chr18:221640
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1370+1800C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221640 | ||||||
chr18:221643
|
C | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0299 | 2 | HG01099.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1370+1797G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221643 | ||||||
chr18:221647
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1370+1793G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221647 | ||||||
chr18:221654
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1370+1786C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221654 | ||||||
chr18:221664
|
A | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG00099.hp1 HG01109.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370+1776T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221664 | ||||||
chr18:221672
|
G | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1370+1768C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221672 | ||||||
chr18:221675
|
C | G | 1 | a0001c0002t0001g0170 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370+1765G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221675 | ||||||
chr18:221702
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0071others(6): Show | 11 | HG01192.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+1738T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221702 | ||||||
chr18:221717
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370+1723A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221717 | ||||||
chr18:221753
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1370+1687G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221753 | ||||||
chr18:221757
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 15 | HG01081.hp2 HG01123.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1370+1683A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221757 | ||||||
chr18:221766
|
A | G | 3 | a0001c0002t0001g0165a0001c0002t0001g0175a0001c0002t0001g0184 | 3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1674T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221766 | ||||||
chr18:221768
|
T | C | 3 | a0001c0002t0001g0165a0001c0002t0001g0175a0001c0002t0001g0184 | 3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1672A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221768 | ||||||
chr18:221769
|
T | C | 3 | a0001c0002t0001g0165a0001c0002t0001g0175a0001c0002t0001g0184 | 3 | HG00423.hp1 HG00673.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1370+1671A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221769 | ||||||
chr18:221791
|
G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1370+1649C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221791 | ||||||
chr18:221820
|
C | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0003t0001g0302 | 3 | HG02055.hp1 NA18966.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1370+1620G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221820 | ||||||
chr18:221830
|
T | C | 1 | a0001c0003t0001g0302 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1370+1610A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221830 | ||||||
chr18:221887
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1370+1553A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221887 | ||||||
chr18:221888
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1370+1552T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221888 | ||||||
chr18:221898
|
G | A | 44 | a0001c0001t0001g0034a0001c0002t0001g0007a0001c0002t0001g0025others(41): Show | 53 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1370+1542C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221898 | ||||||
chr18:221900
|
G | A | 1 | a0001c0002t0001g0176 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1370+1540C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221900 | ||||||
chr18:221903
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02257.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1370+1537A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221903 | ||||||
chr18:221951
|
G | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0205others(4): Show | 10 | HG00544.hp2 HG02074.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370+1489C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221951 | ||||||
chr18:221989
|
T | G | 6 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(3): Show | 7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1370+1451A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 221989 | ||||||
chr18:222167
|
T | C | 16 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0123others(13): Show | 18 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370+1273A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222167 | ||||||
chr18:222227
|
AAAT | A | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1370+1210_1370+121 others(7): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222227 | ||||||
chr18:222229
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1370+1211T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222229 | ||||||
chr18:222266
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1370+1174T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222266 | ||||||
chr18:222334
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1370+1106G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222334 | ||||||
chr18:222467
|
C | T | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1370+973G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222467 | ||||||
chr18:222676
|
AAT | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(54): Show | 73 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1370+762_1370+763d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222676 | ||||||
chr18:222793
|
T | A | 1 | a0001c0002t0001g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1370+647A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222793 | ||||||
chr18:222973
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+467A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 222973 | ||||||
chr18:223185
|
G | A | 48 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1370+255C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223185 | ||||||
chr18:223189
|
C | T | 21 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(18): Show | 25 | HG00280.hp2 HG00642.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1370+251G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223189 | ||||||
chr18:223309
|
G | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1370+131C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223309 | ||||||
chr18:223366
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1370+74T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 17/20 | chr18 | 223366 | ||||||
chr18:223514
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0284 | 2 | HG01175.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1305-9A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223514 | ||||||
chr18:223885
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1304+199C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223885 | ||||||
chr18:223974
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1304+110C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 223974 | ||||||
chr18:224021
|
A | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1304+63T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 16/20 | chr18 | 224021 | ||||||
chr18:224184
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(198): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
splice_region_variant&intron_variant | LOW | c.1209-5G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224184 | ||||||
chr18:224268
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG01109.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1209-89A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224268 | ||||||
chr18:224304
|
C | T | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1209-125G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224304 | ||||||
chr18:224510
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1209-331G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224510 | ||||||
chr18:224526
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00735.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-347G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224526 | ||||||
chr18:224578
|
CA | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(182): Show | 226 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1208+345delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224578 | ||||||
chr18:224668
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1208+256C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224668 | ||||||
chr18:224684
|
ATTC | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+237_1208+239d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224684 | ||||||
chr18:224690
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+234G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224690 | ||||||
chr18:224854
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208+70G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 15/20 | chr18 | 224854 | ||||||
chr18:225005
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-11G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225005 | ||||||
chr18:225009
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1138-15C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225009 | ||||||
chr18:225027
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1138-33C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225027 | ||||||
chr18:225051
|
C | T | 48 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 55 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.1137+38G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225051 | ||||||
chr18:225081
|
A | T | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1137+8T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 14/20 | chr18 | 225081 | ||||||
chr18:225237
|
T | C | 1 | a0001c0002t0001g0169 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1087-98A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 13/20 | chr18 | 225237 | ||||||
chr18:225608
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0157others(1): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020-205T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225608 | ||||||
chr18:225964
|
A | G | 49 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1020-561T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225964 | ||||||
chr18:225985
|
G | A | 48 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(45): Show | 57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1020-582C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 225985 | ||||||
chr18:226011
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0242 | 3 | HG03710.hp1 NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1020-608A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226011 | ||||||
chr18:226055
|
C | T | 2 | a0001c0002t0001g0168a0001c0002t0001g0169 | 2 | NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1020-652G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226055 | ||||||
chr18:226219
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1019+582A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226219 | ||||||
chr18:226334
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+467C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226334 | ||||||
chr18:226420
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1019+381T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226420 | ||||||
chr18:226459
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0220a0001c0001t0001g0304 | 3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1019+342A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226459 | ||||||
chr18:226485
|
A | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(32): Show | 41 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.1019+316T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226485 | ||||||
chr18:226490
|
T | C | 1 | a0001c0002t0001g0189 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1019+311A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226490 | ||||||
chr18:226509
|
G | A | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1019+292C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226509 | ||||||
chr18:226525
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1019+276C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226525 | ||||||
chr18:226634
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1019+167G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226634 | ||||||
chr18:226650
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+151A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226650 | ||||||
chr18:226664
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1019+137T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226664 | ||||||
chr18:226672
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1019+129C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 12/20 | chr18 | 226672 | ||||||
chr18:226928
|
C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-27G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 226928 | ||||||
chr18:227116
|
A | G | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.919-215T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227116 | ||||||
chr18:227314
|
T | TA | 11 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.919-414dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227314 | ||||||
chr18:227325
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG01168.hp2 HG01169.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-424A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227325 | ||||||
chr18:227466
|
C | G | 1 | a0001c0003t0001g0278 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.919-565G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227466 | ||||||
chr18:227472
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.919-571T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227472 | ||||||
chr18:227608
|
G | GTTC | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(196): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.919-710_919-708dup others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227608 | ||||||
chr18:227731
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-830A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227731 | ||||||
chr18:227839
|
T | G | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-938A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227839 | ||||||
chr18:227946
|
T | TA | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(64): Show | 86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.919-1046dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 227946 | ||||||
chr18:228001
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.919-1100A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228001 | ||||||
chr18:228015
|
T | G | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919-1114A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228015 | ||||||
chr18:228092
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG00735.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-1191G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228092 | ||||||
chr18:228147
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.919-1246C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228147 | ||||||
chr18:228152
|
G | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.919-1251C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228152 | ||||||
chr18:228303
|
A | G | 1 | a0001c0003t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.919-1402T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228303 | ||||||
chr18:228346
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-1445C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228346 | ||||||
chr18:228388
|
C | A | 1 | a0001c0001t0001g0300 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.919-1487G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228388 | ||||||
chr18:228527
|
G | GA | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(178): Show | 222 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.919-1627dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228527 | ||||||
chr18:228537
|
C | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.919-1636G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228537 | ||||||
chr18:228640
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.919-1739G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228640 | ||||||
chr18:228875
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0231 | 2 | NA18967.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.919-1974A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 228875 | ||||||
chr18:229038
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0001g0081others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-2137A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229038 | ||||||
chr18:229074
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0157others(1): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-2173G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229074 | ||||||
chr18:229112
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-2211G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229112 | ||||||
chr18:229255
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919-2354G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229255 | ||||||
chr18:229402
|
C | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-2501G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229402 | ||||||
chr18:229453
|
G | A | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-2552C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229453 | ||||||
chr18:229494
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.919-2593T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229494 | ||||||
chr18:229518
|
TA | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(193): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.919-2618delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229518 | ||||||
chr18:229616
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.919-2715C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229616 | ||||||
chr18:229676
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.919-2775G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229676 | ||||||
chr18:229710
|
A | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0058others(10): Show | 16 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919-2809T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229710 | ||||||
chr18:229844
|
TCTC | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-2946_919-2944d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229844 | ||||||
chr18:229853
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.919-2952G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229853 | ||||||
chr18:229887
|
C | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-2986G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229887 | ||||||
chr18:229888
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0058others(10): Show | 16 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919-2987C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 229888 | ||||||
chr18:230444
|
T | G | 1 | a0001c0005t0002g0048 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.919-3543A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230444 | ||||||
chr18:230482
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-3581G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230482 | ||||||
chr18:230634
|
C | G | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.919-3733G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230634 | ||||||
chr18:230739
|
T | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(29): Show | 38 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.919-3838A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230739 | ||||||
chr18:230756
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.919-3855C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230756 | ||||||
chr18:230821
|
G | C | 1 | a0001c0002t0001g0027 | 2 | HG02129.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.919-3920C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230821 | ||||||
chr18:230848
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-3947C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230848 | ||||||
chr18:230924
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919-4023C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230924 | ||||||
chr18:230960
|
G | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-4059C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 230960 | ||||||
chr18:231035
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919-4134C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231035 | ||||||
chr18:231063
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.919-4162A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231063 | ||||||
chr18:231079
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.919-4178T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231079 | ||||||
chr18:231242
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-4341G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231242 | ||||||
chr18:231323
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.919-4422A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231323 | ||||||
chr18:231453
|
CAT | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0007t0001g0115 | 3 | HG06807.hp1 NA18906.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.919-4554_919-4553d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231453 | ||||||
chr18:231457
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.919-4556A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231457 | ||||||
chr18:231503
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.919-4602G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231503 | ||||||
chr18:231730
|
C | G | 2 | a0001c0001t0001g0008a0001c0007t0001g0115 | 4 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-4829G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 231730 | ||||||
chr18:232114
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.919-5213C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232114 | ||||||
chr18:232280
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-5379T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232280 | ||||||
chr18:232337
|
A | G | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-5436T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232337 | ||||||
chr18:232340
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.919-5439G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232340 | ||||||
chr18:232462
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919-5561T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232462 | ||||||
chr18:232508
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-5607A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232508 | ||||||
chr18:232791
|
T | TGAA | 35 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(32): Show | 41 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.919-5891_919-5890i others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232791 | ||||||
chr18:232961
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-6060A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232961 | ||||||
chr18:232995
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0220a0001c0001t0001g0304 | 3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919-6094G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 232995 | ||||||
chr18:233016
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.919-6115G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233016 | ||||||
chr18:233217
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919-6316T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233217 | ||||||
chr18:233329
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.919-6428C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233329 | ||||||
chr18:233379
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.919-6478C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233379 | ||||||
chr18:233443
|
G | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0045a0001c0001t0002g0049others(9): Show | 15 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.919-6542C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233443 | ||||||
chr18:233486
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.919-6585A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233486 | ||||||
chr18:233542
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919-6641G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233542 | ||||||
chr18:233547
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-6646G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233547 | ||||||
chr18:233830
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919-6929A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 233830 | ||||||
chr18:234138
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.919-7237C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234138 | ||||||
chr18:234313
|
C | T | 1 | a0001c0002t0001g0176 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.919-7412G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234313 | ||||||
chr18:234418
|
T | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG03098.hp1 HG03453.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-7517A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234418 | ||||||
chr18:234473
|
T | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.919-7572A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234473 | ||||||
chr18:234502
|
G | C | 2 | a0001c0001t0001g0097a0001c0001t0002g0014 | 3 | HG00642.hp2 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.919-7601C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234502 | ||||||
chr18:234554
|
G | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-7653C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234554 | ||||||
chr18:234555
|
T | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-7654A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234555 | ||||||
chr18:234627
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0070 | 4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-7726G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234627 | ||||||
chr18:234630
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.919-7729G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234630 | ||||||
chr18:234661
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.919-7760G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234661 | ||||||
chr18:234679
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.919-7778C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234679 | ||||||
chr18:234773
|
T | TAAC | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(189): Show | 233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.919-7873_919-7872i others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234773 | ||||||
chr18:234790
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.919-7889A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 234790 | ||||||
chr18:235001
|
T | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-8100A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235001 | ||||||
chr18:235083
|
C | CT | 6 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(3): Show | 7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-8183dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235083 | ||||||
chr18:235085
|
A | AT | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(157): Show | 197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.919-8185dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | ||||||
chr18:235085
|
A | ATT | 20 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0058others(17): Show | 21 | HG00423.hp2 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.919-8186_919-8185d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | ||||||
chr18:235085
|
A | T | 6 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(3): Show | 7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-8184T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | ||||||
chr18:235085
|
AT | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0236a0001c0001t0001g0255others(3): Show | 6 | HG01169.hp2 HG03041.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-8185delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235085 | ||||||
chr18:235086
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.919-8185A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235086 | ||||||
chr18:235087
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.919-8186A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235087 | ||||||
chr18:235146
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919-8245A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235146 | ||||||
chr18:235256
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.919-8355A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235256 | ||||||
chr18:235383
|
G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-8482C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235383 | ||||||
chr18:235420
|
C | G | 2 | a0001c0002t0001g0190a0001c0002t0001g0191 | 2 | NA18963.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.919-8519G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235420 | ||||||
chr18:235420
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919-8519G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235420 | ||||||
chr18:235774
|
C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.919-8873G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235774 | ||||||
chr18:235780
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.919-8879A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235780 | ||||||
chr18:235928
|
A | G | 13 | a0001c0001t0001g0148a0001c0001t0002g0006a0001c0001t0002g0045others(10): Show | 16 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.919-9027T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 235928 | ||||||
chr18:236019
|
A | G | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.919-9118T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236019 | ||||||
chr18:236244
|
T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-9343A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236244 | ||||||
chr18:236350
|
CT | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(116): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.919-9450delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | ||||||
chr18:236350
|
CTT | C | 62 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(59): Show | 75 | HG00423.hp1 HG00673.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-9451_919-9450d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | ||||||
chr18:236350
|
CTTT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(91): Show | 118 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.919-9452_919-9450d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | ||||||
chr18:236350
|
CTTTT | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 10 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.919-9453_919-9450d others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236350 | ||||||
chr18:236352
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919-9451A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236352 | ||||||
chr18:236381
|
A | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.919-9480T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236381 | ||||||
chr18:236437
|
G | A | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.919-9536C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236437 | ||||||
chr18:236451
|
G | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(54): Show | 75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-9550C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236451 | ||||||
chr18:236463
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919-9562G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236463 | ||||||
chr18:236471
|
TCAGCCTC others(18): Show |
T | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.919-9595_919-9571d others(27): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236471 | ||||||
chr18:236491
|
GA | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(178): Show | 221 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.919-9591delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236491 | ||||||
chr18:236508
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.919-9607A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236508 | ||||||
chr18:236518
|
G | A | 1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919-9617C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236518 | ||||||
chr18:236523
|
A | AT | 55 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(52): Show | 65 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.919-9623dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236523 | ||||||
chr18:236718
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.918+9606T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 236718 | ||||||
chr18:237017
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+9307G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237017 | ||||||
chr18:237063
|
G | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01167.hp1 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.918+9261C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237063 | ||||||
chr18:237157
|
A | AT | 25 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0058others(22): Show | 31 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.918+9166dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | ||||||
chr18:237157
|
AT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(88): Show | 117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.918+9166delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | ||||||
chr18:237157
|
ATT | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0021others(38): Show | 45 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+9165_918+9166d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237157 | ||||||
chr18:237177
|
T | G | 20 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(17): Show | 23 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.918+9147A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237177 | ||||||
chr18:237230
|
G | C | 1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918+9094C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237230 | ||||||
chr18:237301
|
TGC | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+9021_918+9022d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237301 | ||||||
chr18:237607
|
GA | G | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+8716delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237607 | ||||||
chr18:237653
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.918+8671G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237653 | ||||||
chr18:237663
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(183): Show | 227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.918+8661C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237663 | ||||||
chr18:237838
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+8486T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237838 | ||||||
chr18:237843
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0151others(2): Show | 7 | HG01106.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+8481G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237843 | ||||||
chr18:237915
|
A | G | 1 | a0001c0002t0001g0183 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.918+8409T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 237915 | ||||||
chr18:238024
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+8300C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238024 | ||||||
chr18:238064
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.918+8260G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238064 | ||||||
chr18:238128
|
G | T | 1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.918+8196C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238128 | ||||||
chr18:238213
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+8110dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238213 | ||||||
chr18:238475
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.918+7849C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238475 | ||||||
chr18:238554
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0077a0001c0001t0001g0088others(2): Show | 7 | HG01175.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+7770C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238554 | ||||||
chr18:238596
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.918+7728C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238596 | ||||||
chr18:238702
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.918+7622G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238702 | ||||||
chr18:238715
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+7609A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238715 | ||||||
chr18:238883
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.918+7441C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238883 | ||||||
chr18:238970
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0220a0001c0001t0001g0304 | 3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.918+7354T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 238970 | ||||||
chr18:239019
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.918+7305T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239019 | ||||||
chr18:239041
|
CTAT | C | 6 | a0001c0002t0001g0028a0001c0002t0001g0179a0001c0002t0001g0180others(3): Show | 7 | HG01081.hp2 HG01993.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+7280_918+7282d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239041 | ||||||
chr18:239052
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.918+7272A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239052 | ||||||
chr18:239062
|
T | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+7262A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239062 | ||||||
chr18:239289
|
C | T | 49 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+7035G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239289 | ||||||
chr18:239405
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.918+6919G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239405 | ||||||
chr18:239463
|
C | A | 1 | a0001c0001t0001g0238 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.918+6861G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239463 | ||||||
chr18:239672
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.918+6652G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239672 | ||||||
chr18:239855
|
A | T | 1 | a0001c0001t0001g0285 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+6469T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239855 | ||||||
chr18:239990
|
A | AT | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(189): Show | 233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.918+6333_918+6334i others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 239990 | ||||||
chr18:240098
|
A | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG02257.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.918+6226T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240098 | ||||||
chr18:240366
|
C | T | 1 | a0001c0003t0001g0269 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.918+5958G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240366 | ||||||
chr18:240436
|
T | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+5888A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240436 | ||||||
chr18:240552
|
T | TTTGGCTA | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+5765_918+5771d others(9): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240552 | ||||||
chr18:240616
|
A | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(29): Show | 38 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.918+5708T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240616 | ||||||
chr18:240675
|
T | C | 20 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 24 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.918+5649A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240675 | ||||||
chr18:240927
|
A | G | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.918+5397T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 240927 | ||||||
chr18:241147
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.918+5177G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241147 | ||||||
chr18:241268
|
T | C | 1 | a0001c0002t0001g0164 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.918+5056A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241268 | ||||||
chr18:241347
|
G | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.918+4977C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241347 | ||||||
chr18:241482
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.918+4842A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241482 | ||||||
chr18:241680
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.918+4644T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241680 | ||||||
chr18:241764
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0200 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.918+4560A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241764 | ||||||
chr18:241874
|
C | T | 5 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0217others(2): Show | 6 | HG00621.hp1 HG02027.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+4450G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241874 | ||||||
chr18:241993
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.918+4331C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 241993 | ||||||
chr18:242201
|
G | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+4123C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242201 | ||||||
chr18:242202
|
CGTGGTGG others(61): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.918+4054_918+4121d others(70): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242202 | ||||||
chr18:242214
|
C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+4110G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242214 | ||||||
chr18:242215
|
G | A | 1 | a0001c0001t0001g0034 | 2 | NA18939.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.918+4109C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242215 | ||||||
chr18:242268
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(179): Show | 220 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.918+4056G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242268 | ||||||
chr18:242283
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.918+4041G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242283 | ||||||
chr18:242350
|
C | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(31): Show | 40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.918+3974G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242350 | ||||||
chr18:242369
|
T | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(31): Show | 40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.918+3955A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242369 | ||||||
chr18:242442
|
C | CA | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+3881dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242442 | ||||||
chr18:242442
|
CA | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.918+3881delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242442 | ||||||
chr18:242489
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.918+3835C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242489 | ||||||
chr18:242494
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(54): Show | 75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.918+3830T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242494 | ||||||
chr18:242855
|
AAACACCA others(3): Show |
A | 1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+3459_918+3468d others(12): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242855 | ||||||
chr18:242912
|
T | G | 1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+3412A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 242912 | ||||||
chr18:243126
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0209others(10): Show | 19 | HG00438.hp1 HG02074.hp2 HG03710.hp1 others(16): Show |
intron_variant | MODIFIER | c.918+3198A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243126 | ||||||
chr18:243219
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+3105A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243219 | ||||||
chr18:243430
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.918+2894G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243430 | ||||||
chr18:243468
|
G | C | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+2856C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243468 | ||||||
chr18:243499
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.918+2825A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243499 | ||||||
chr18:243545
|
A | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0040others(24): Show | 32 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.918+2779T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243545 | ||||||
chr18:243546
|
AT | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+2777delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243546 | ||||||
chr18:243547
|
T | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(139): Show | 176 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.918+2777A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243547 | ||||||
chr18:243549
|
T | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0105 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.918+2775A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243549 | ||||||
chr18:243754
|
T | TCGGGGGG others(3): Show |
1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+2569_918+2570i others(12): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243754 | ||||||
chr18:243820
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0299 | 2 | HG01099.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.918+2504A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243820 | ||||||
chr18:243943
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.918+2381A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 243943 | ||||||
chr18:244065
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0206 | 3 | HG02080.hp2 NA18994.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.918+2259A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244065 | ||||||
chr18:244125
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.918+2199T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244125 | ||||||
chr18:244378
|
T | A | 1 | a0001c0002t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.918+1946A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244378 | ||||||
chr18:244553
|
T | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+1771A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244553 | ||||||
chr18:244768
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+1556G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244768 | ||||||
chr18:244872
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0151others(2): Show | 7 | HG01106.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+1452A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244872 | ||||||
chr18:244908
|
CCTT | C | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+1413_918+1415d others(5): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 244908 | ||||||
chr18:245056
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.918+1268A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245056 | ||||||
chr18:245087
|
G | C | 2 | a0001c0002t0001g0029a0001c0002t0001g0183 | 3 | HG02015.hp2 HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.918+1237C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245087 | ||||||
chr18:245168
|
A | AAT | 9 | a0001c0001t0001g0008a0001c0001t0001g0121a0001c0001t0001g0125others(6): Show | 11 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+1154_918+1155d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245168 | ||||||
chr18:245179
|
A | C | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.918+1145T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245179 | ||||||
chr18:245249
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.918+1075T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245249 | ||||||
chr18:245284
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.918+1040A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245284 | ||||||
chr18:245465
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.918+859C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245465 | ||||||
chr18:245888
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.918+436C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245888 | ||||||
chr18:245971
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.918+353G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 245971 | ||||||
chr18:246057
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.918+267A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246057 | ||||||
chr18:246063
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.918+261A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246063 | ||||||
chr18:246199
|
T | C | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.918+125A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246199 | ||||||
chr18:246265
|
A | T | 1 | a0001c0002t0001g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.918+59T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246265 | ||||||
chr18:246297
|
T | G | 1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.918+27A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 11/20 | chr18 | 246297 | ||||||
chr18:246537
|
T | C | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-82A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246537 | ||||||
chr18:246549
|
A | T | 1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787-94T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246549 | ||||||
chr18:246550
|
A | T | 1 | a0001c0002t0001g0188 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787-95T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246550 | ||||||
chr18:246568
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.787-113T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246568 | ||||||
chr18:246675
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.787-220G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246675 | ||||||
chr18:246677
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.787-222T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246677 | ||||||
chr18:246916
|
C | CA | 14 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0042others(11): Show | 20 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.787-462dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | ||||||
chr18:246916
|
C | CAA | 5 | a0001c0001t0001g0035a0001c0001t0001g0218a0001c0001t0001g0223others(2): Show | 6 | HG00673.hp2 NA19002.hp2 NA19060.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-463_787-462dup others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | ||||||
chr18:246916
|
CA | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(84): Show | 113 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.787-462delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | ||||||
chr18:246916
|
CAA | C | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-463_787-462del others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | ||||||
chr18:246916
|
CAAA | C | 37 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 43 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.787-464_787-462del others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246916 | ||||||
chr18:246930
|
A | C | 2 | a0001c0001t0001g0126a0001c0003t0001g0280 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.787-475T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246930 | ||||||
chr18:246935
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.787-480T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246935 | ||||||
chr18:246970
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.787-515C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 246970 | ||||||
chr18:247127
|
C | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.787-672G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247127 | ||||||
chr18:247378
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.786+471A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247378 | ||||||
chr18:247509
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+340C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247509 | ||||||
chr18:247510
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+339T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247510 | ||||||
chr18:247521
|
G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+328C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247521 | ||||||
chr18:247568
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786+281A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247568 | ||||||
chr18:247722
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.786+127A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247722 | ||||||
chr18:247834
|
T | G | 47 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.786+15A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 10/20 | chr18 | 247834 | ||||||
chr18:247972
|
G | A | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-15C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 247972 | ||||||
chr18:248187
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.678-230T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248187 | ||||||
chr18:248228
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.678-271G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248228 | ||||||
chr18:248254
|
A | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.678-297T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248254 | ||||||
chr18:248266
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 7 | HG02257.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-309T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248266 | ||||||
chr18:248268
|
C | G | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-311G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248268 | ||||||
chr18:248279
|
G | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.678-322C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248279 | ||||||
chr18:248342
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.678-385A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248342 | ||||||
chr18:248481
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.678-524A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248481 | ||||||
chr18:248710
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.678-753G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248710 | ||||||
chr18:248838
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.678-881G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248838 | ||||||
chr18:248912
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(54): Show | 75 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.678-955C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248912 | ||||||
chr18:248992
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.678-1035A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 248992 | ||||||
chr18:249228
|
G | A | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.678-1271C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249228 | ||||||
chr18:249359
|
G | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0256 | 3 | HG02027.hp1 HG02165.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.678-1402C>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249359 | ||||||
chr18:249372
|
A | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0060others(7): Show | 13 | HG00544.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.678-1415T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249372 | ||||||
chr18:249468
|
C | T | 3 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308 | 3 | HG01109.hp1 HG01256.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.678-1511G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249468 | ||||||
chr18:249472
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 215 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.678-1515T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249472 | ||||||
chr18:249594
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.678-1637T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249594 | ||||||
chr18:249606
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(42): Show | 56 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.678-1649C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249606 | ||||||
chr18:249653
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.678-1696G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249653 | ||||||
chr18:249668
|
G | GA | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(61): Show | 86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.678-1712dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249668 | ||||||
chr18:249668
|
G | GAA | 36 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 41 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.678-1713_678-1712d others(4): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249668 | ||||||
chr18:249910
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.678-1953T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249910 | ||||||
chr18:249939
|
T | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.678-1982A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 249939 | ||||||
chr18:250018
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.678-2061G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250018 | ||||||
chr18:250047
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(189): Show | 233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.678-2090A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250047 | ||||||
chr18:250058
|
A | G | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(15): Show | 21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.678-2101T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250058 | ||||||
chr18:250073
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.678-2116A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250073 | ||||||
chr18:250462
|
A | C | 1 | a0001c0001t0001g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.677+2077T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250462 | ||||||
chr18:250539
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.677+2000G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250539 | ||||||
chr18:250589
|
A | C | 99 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(96): Show | 116 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(113): Show |
intron_variant | MODIFIER | c.677+1950T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250589 | ||||||
chr18:250616
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.677+1923A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 250616 | ||||||
chr18:251017
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.677+1522A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251017 | ||||||
chr18:251123
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.677+1416A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251123 | ||||||
chr18:251558
|
T | C | 47 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.677+981A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251558 | ||||||
chr18:251565
|
G | GA | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.677+973dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251565 | ||||||
chr18:251728
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.677+811C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251728 | ||||||
chr18:251765
|
C | T | 50 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(47): Show | 60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.677+774G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251765 | ||||||
chr18:251789
|
C | A | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG00733.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+750G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251789 | ||||||
chr18:251954
|
G | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG00438.hp2 HG02027.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.677+585C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 251954 | ||||||
chr18:252038
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.677+501G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252038 | ||||||
chr18:252043
|
AT | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.677+495delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252043 | ||||||
chr18:252082
|
T | C | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.677+457A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252082 | ||||||
chr18:252156
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.677+383C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252156 | ||||||
chr18:252253
|
T | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677+286A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252253 | ||||||
chr18:252268
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.677+271G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252268 | ||||||
chr18:252436
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.677+103T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 9/20 | chr18 | 252436 | ||||||
chr18:252769
|
A | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.604-157T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252769 | ||||||
chr18:252769
|
AT | A | 1 | a0001c0001t0001g0011 | 3 | HG00621.hp2 NA18950.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.604-158delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252769 | ||||||
chr18:252795
|
G | C | 48 | a0001c0001t0001g0142a0001c0002t0001g0007a0001c0002t0001g0025others(45): Show | 57 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.604-183C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252795 | ||||||
chr18:252925
|
A | C | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.604-313T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252925 | ||||||
chr18:252998
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.604-386T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 252998 | ||||||
chr18:253216
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.604-604A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253216 | ||||||
chr18:253305
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.604-693C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253305 | ||||||
chr18:253321
|
G | A | 1 | a0001c0002t0001g0189 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.604-709C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253321 | ||||||
chr18:253336
|
A | T | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0163 | 3 | NA18954.hp2 NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.604-724T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253336 | ||||||
chr18:253506
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+767A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253506 | ||||||
chr18:253587
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.603+686C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253587 | ||||||
chr18:253902
|
A | AT | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(59): Show | 80 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.603+370dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | ||||||
chr18:253902
|
A | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.603+371T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | ||||||
chr18:253902
|
AT | A | 88 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0016others(85): Show | 105 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.603+370delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 253902 | ||||||
chr18:254013
|
C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.603+260G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 254013 | ||||||
chr18:254172
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.603+101T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 8/20 | chr18 | 254172 | ||||||
chr18:254368
|
C | CA | 6 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521-14dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254368 | ||||||
chr18:254565
|
CTT | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-212_521-211del others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254565 | ||||||
chr18:254613
|
A | G | 2 | a0001c0003t0001g0280a0001c0003t0001g0281 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.521-258T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254613 | ||||||
chr18:254640
|
G | A | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-285C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254640 | ||||||
chr18:254762
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.521-407G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254762 | ||||||
chr18:254762
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.521-407G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254762 | ||||||
chr18:254798
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.521-443T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254798 | ||||||
chr18:254817
|
A | AT | 6 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 8 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.521-463dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254817 | ||||||
chr18:254962
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.521-607T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 254962 | ||||||
chr18:255101
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.521-746T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255101 | ||||||
chr18:255143
|
G | A | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.521-788C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255143 | ||||||
chr18:255156
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0304 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.521-801T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255156 | ||||||
chr18:255209
|
G | A | 2 | a0001c0002t0001g0190a0001c0002t0001g0191 | 2 | NA18963.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.521-854C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255209 | ||||||
chr18:255210
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.521-855T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255210 | ||||||
chr18:255552
|
G | A | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(31): Show | 40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.521-1197C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255552 | ||||||
chr18:255581
|
T | A | 2 | a0001c0003t0001g0278a0001c0003t0001g0279 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.521-1226A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255581 | ||||||
chr18:255622
|
G | A | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.521-1267C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255622 | ||||||
chr18:255799
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.521-1444T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255799 | ||||||
chr18:255875
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.521-1520T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 255875 | ||||||
chr18:256008
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.521-1653A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256008 | ||||||
chr18:256043
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.521-1688T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256043 | ||||||
chr18:256138
|
A | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.521-1783T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256138 | ||||||
chr18:256200
|
A | AC | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(189): Show | 233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.521-1846dupG | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256200 | ||||||
chr18:256238
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.521-1883C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256238 | ||||||
chr18:256314
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.521-1959A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256314 | ||||||
chr18:256900
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.520+2280G>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256900 | ||||||
chr18:256976
|
G | A | 47 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.520+2204C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 256976 | ||||||
chr18:257104
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0303 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520+2076C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257104 | ||||||
chr18:257377
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(7): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.520+1803T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257377 | ||||||
chr18:257661
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520+1519T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257661 | ||||||
chr18:257671
|
G | A | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.520+1509C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257671 | ||||||
chr18:257785
|
TA | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.520+1394delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257785 | ||||||
chr18:257968
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520+1212A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 257968 | ||||||
chr18:258284
|
C | G | 97 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(94): Show | 114 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.520+896G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258284 | ||||||
chr18:258294
|
G | A | 19 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 22 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.520+886C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258294 | ||||||
chr18:258324
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.520+856T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258324 | ||||||
chr18:258681
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.520+499T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258681 | ||||||
chr18:258685
|
G | A | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.520+495C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258685 | ||||||
chr18:258778
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02055.hp2 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.520+402G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258778 | ||||||
chr18:258809
|
T | C | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(15): Show | 21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.520+371A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 258809 | ||||||
chr18:259148
|
G | A | 50 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(47): Show | 60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.520+32C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 7/20 | chr18 | 259148 | ||||||
chr18:259379
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.425-104T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 6/20 | chr18 | 259379 | ||||||
chr18:259743
|
C | T | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376-13G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259743 | ||||||
chr18:259758
|
T | C | 2 | a0001c0003t0001g0280a0001c0003t0001g0281 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.376-28A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259758 | ||||||
chr18:259789
|
A | G | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.376-59T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259789 | ||||||
chr18:259800
|
G | GA | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(31): Show | 40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.376-71dupT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259800 | ||||||
chr18:259944
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0113 | 2 | HG00408.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.376-214T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 259944 | ||||||
chr18:260040
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.375+146C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260040 | ||||||
chr18:260041
|
AG | A | 50 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044others(47): Show | 60 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.375+144delC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260041 | ||||||
chr18:260051
|
A | ATATAATT others(309): Show |
1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.375+134_375+135ins others(316): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260051 | ||||||
chr18:260108
|
TA | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.375+77delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260108 | ||||||
chr18:260109
|
A | T | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+77T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260109 | ||||||
chr18:260140
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.375+46A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260140 | ||||||
chr18:260152
|
T | G | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.375+34A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 5/20 | chr18 | 260152 | ||||||
chr18:260473
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0218a0001c0001t0001g0249others(4): Show | 8 | HG00673.hp2 HG02015.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.257-169A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260473 | ||||||
chr18:260504
|
T | C | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(15): Show | 21 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.257-200A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260504 | ||||||
chr18:260597
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(186): Show | 230 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.257-293A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260597 | ||||||
chr18:260684
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.257-380A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260684 | ||||||
chr18:260966
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.257-662C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 260966 | ||||||
chr18:261106
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.257-802A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261106 | ||||||
chr18:261268
|
A | G | 49 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 56 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.257-964T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261268 | ||||||
chr18:261278
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.257-974T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261278 | ||||||
chr18:261279
|
T | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.257-975A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261279 | ||||||
chr18:261279
|
T | C | 1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.257-975A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261279 | ||||||
chr18:261346
|
C | T | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.257-1042G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261346 | ||||||
chr18:261387
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.257-1083T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261387 | ||||||
chr18:261500
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.257-1196T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261500 | ||||||
chr18:261536
|
C | T | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.257-1232G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261536 | ||||||
chr18:261610
|
G | A | 3 | a0001c0002t0001g0030a0001c0002t0001g0193a0001c0002t0001g0194 | 4 | NA18939.hp1 NA19010.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.257-1306C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261610 | ||||||
chr18:261733
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.257-1429G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261733 | ||||||
chr18:261903
|
T | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.257-1599A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 261903 | ||||||
chr18:262000
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.257-1696G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262000 | ||||||
chr18:262187
|
C | T | 1 | a0001c0007t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.256+1839G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262187 | ||||||
chr18:262259
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.256+1767A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262259 | ||||||
chr18:262456
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200 | 3 | HG02109.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.256+1570G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262456 | ||||||
chr18:262526
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.256+1500A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262526 | ||||||
chr18:262589
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.256+1437C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262589 | ||||||
chr18:262597
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.256+1429C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262597 | ||||||
chr18:262599
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.256+1427G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262599 | ||||||
chr18:262616
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.256+1410C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262616 | ||||||
chr18:262850
|
GAATT | G | 47 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.256+1172_256+1175d others(6): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 262850 | ||||||
chr18:263137
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+889C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263137 | ||||||
chr18:263174
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0002g0014 | 4 | HG00642.hp2 HG01175.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.256+852C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263174 | ||||||
chr18:263198
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.256+828C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263198 | ||||||
chr18:263227
|
C | CA | 47 | a0001c0002t0001g0007a0001c0002t0001g0025a0001c0002t0001g0026others(44): Show | 56 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.256+798_256+799ins others(1): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263227 | ||||||
chr18:263368
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.256+658G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263368 | ||||||
chr18:263375
|
G | A | 1 | a0001c0001t0001g0019 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.256+651C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263375 | ||||||
chr18:263399
|
G | A | 1 | a0001c0001t0001g0008 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.256+627C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263399 | ||||||
chr18:263514
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.256+512T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263514 | ||||||
chr18:263600
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.256+426A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263600 | ||||||
chr18:263641
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.256+385C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263641 | ||||||
chr18:263677
|
A | G | 1 | a0001c0001t0001g0016 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.256+349T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263677 | ||||||
chr18:263679
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.256+347G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263679 | ||||||
chr18:263687
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.256+339A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263687 | ||||||
chr18:263698
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.256+328G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263698 | ||||||
chr18:263718
|
T | C | 12 | a0001c0001t0002g0006a0001c0001t0002g0045a0001c0001t0002g0049others(9): Show | 15 | HG00280.hp2 HG01099.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.256+308A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 263718 | ||||||
chr18:264012
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0039others(30): Show | 37 | HG00280.hp2 HG01099.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.256+14C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 4/20 | chr18 | 264012 | ||||||
chr18:264330
|
A | G | 2 | a0001c0001t0001g0008a0001c0007t0001g0115 | 4 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-238T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264330 | ||||||
chr18:264341
|
T | C | 1 | a0001c0006t0001g0195 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.190-249A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264341 | ||||||
chr18:264342
|
A | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG01167.hp1 HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.190-250T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264342 | ||||||
chr18:264352
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0070 | 4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-260C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264352 | ||||||
chr18:264431
|
T | G | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(290): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.190-339A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264431 | ||||||
chr18:264882
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.189+421C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264882 | ||||||
chr18:264904
|
TGAG | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+396_189+398del others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264904 | ||||||
chr18:264954
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+349A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 264954 | ||||||
chr18:265147
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.189+156C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 265147 | ||||||
chr18:265237
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.189+66G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 3/20 | chr18 | 265237 | ||||||
chr18:265370
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.129-7T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 2/20 | chr18 | 265370 | ||||||
chr18:265406
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.129-43C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 2/20 | chr18 | 265406 | ||||||
chr18:265677
|
C | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0217 | 2 | HG00621.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.55-147G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265677 | ||||||
chr18:265714
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0205others(4): Show | 10 | HG00544.hp2 HG02074.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-184T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265714 | ||||||
chr18:265808
|
CA | C | 68 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(65): Show | 80 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.55-279delT | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265808 | ||||||
chr18:265846
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.55-316C>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 265846 | ||||||
chr18:266146
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0070 | 4 | HG02976.hp2 HG03239.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-616A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266146 | ||||||
chr18:266177
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.55-647A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266177 | ||||||
chr18:266222
|
T | C | 1 | a0001c0002t0001g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.55-692A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266222 | ||||||
chr18:266251
|
T | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.55-721A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266251 | ||||||
chr18:266457
|
A | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0038others(31): Show | 40 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.55-927T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266457 | ||||||
chr18:266539
|
A | AT | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(121): Show | 154 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.55-1010dupA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | ||||||
chr18:266539
|
A | ATT | 59 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 66 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.55-1011_55-1010dup others(2): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | ||||||
chr18:266539
|
A | ATTT | 9 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0118others(6): Show | 11 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1012_55-1010dup others(3): Show |
THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | ||||||
chr18:266539
|
A | T | 1 | a0001c0001t0001g0264 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.55-1009T>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | ||||||
chr18:266539
|
AT | A | 6 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | HG01071.hp1 HG02698.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1010delA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266539 | ||||||
chr18:266552
|
T | A | 1 | a0001c0001t0001g0264 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.55-1022A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266552 | ||||||
chr18:266568
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.55-1038A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266568 | ||||||
chr18:266627
|
G | C | 1 | a0001c0002t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.55-1097C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266627 | ||||||
chr18:266725
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.55-1195G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266725 | ||||||
chr18:266828
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0305 | 2 | HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.54+1138G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266828 | ||||||
chr18:266848
|
C | T | 23 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(20): Show | 26 | HG00280.hp2 HG01099.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.54+1118G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 266848 | ||||||
chr18:267008
|
CGT | C | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 54 | HG00733.hp1 HG01070.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.54+956_54+957delAC | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267008 | ||||||
chr18:267014
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0157others(1): Show | 6 | HG02258.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+952A>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267014 | ||||||
chr18:267019
|
G | GTA | 3 | a0001c0001t0001g0303a0001c0003t0001g0301a0001c0003t0001g0302 | 3 | HG02055.hp1 HG02602.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54+945_54+946dupTA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267019 | ||||||
chr18:267019
|
GTA | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.54+945_54+946delTA | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267019 | ||||||
chr18:267023
|
A | G | 1 | a0001c0001t0002g0014 | 2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.54+943T>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267023 | ||||||
chr18:267048
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.54+918G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267048 | ||||||
chr18:267262
|
C | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(189): Show | 233 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.54+704G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267262 | ||||||
chr18:267303
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.54+663A>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267303 | ||||||
chr18:267367
|
A | C | 24 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 29 | HG00280.hp2 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.54+599T>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267367 | ||||||
chr18:267496
|
G | C | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+470C>G | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267496 | ||||||
chr18:267499
|
T | A | 1 | a0001c0001t0001g0312 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.54+467A>T | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267499 | ||||||
chr18:267625
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0043a0001c0001t0001g0044 | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+341G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267625 | ||||||
chr18:267768
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+198G>A | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267768 | ||||||
chr18:267923
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.54+43G>C | THOC1 | ENSG00000079134.13 | transcript | ENST00000261600.11 | protein_coding | 1/20 | chr18 | 267923 |