geneid | 79600 |
---|---|
ensemblid | ENSG00000204852.17 |
hgncid | 26113 |
symbol | TCTN1 |
name | tectonic family member 1 |
refseq_nuc | NM_001082538.3 |
refseq_prot | NP_001076007.1 |
ensembl_nuc | ENST00000397659.9 |
ensembl_prot | ENSP00000380779.4 |
mane_status | MANE Select |
chr | chr12 |
start | 110614129 |
end | 110649430 |
strand | + |
ver | v1.2 |
region | chr12:110614129-110649430 |
region5000 | chr12:110609129-110654430 |
regionname0 | TCTN1_chr12_110614129_110649430 |
regionname5000 | TCTN1_chr12_110609129_110654430 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 592 | 270 | 81 | 56 | 85 | 16 | 30 | 59 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0002 | 0/0 | 592 | 5 | 0 | 2 | 1 | 0 | 2 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0003 | 0/0 | 592 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0004 | 0/0 | 592 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0005 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0006 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0007 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0008 | 0/0 | 592 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0009 | 0/0 | 592 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1779 | 259 | 73 | 53 | 85 | 16 | 30 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0002 | 0/0 | 1779 | 10 | 7 | 3 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0003 | 0/0 | 1779 | 5 | 0 | 2 | 1 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0004 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0005 | 0/0 | 1779 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0006 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0007 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0009 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0010 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
c0011 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 21 | 1 | 1 | 17 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0002 | 0/0 | 20 | 0 | 3 | 11 | 0 | 6 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0004 | 0/0 | 6 | 1 | 1 | 0 | 3 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1779 | 259 | 73 | 53 | 85 | 16 | 30 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0001c0002 | 0/0 | 1779 | 10 | 7 | 3 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0001c0007 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0002c0003 | 0/0 | 1779 | 5 | 0 | 2 | 1 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0003c0004 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0004c0005 | 0/0 | 1779 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0005c0006 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0006c0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0007c0010 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0008c0009 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0009c0011 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2221 | 259 | 73 | 53 | 85 | 16 | 30 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0001c0002t0001 | 0/0 | 2221 | 10 | 7 | 3 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0001c0007t0001 | 0/0 | 2221 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0002c0003t0001 | 0/0 | 2221 | 5 | 0 | 2 | 1 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0003c0004t0001 | 0/0 | 2221 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0004c0005t0001 | 0/0 | 2221 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0005c0006t0002 | 0/0 | 2221 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0006c0008t0001 | 0/0 | 2221 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0007c0010t0001 | 0/0 | 2221 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0008c0009t0001 | 0/0 | 2221 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
a0009c0011t0001 | 0/0 | 2221 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | copy fasta | chr12 | 110609129 | 110654430 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 21 | 1 | 1 | 17 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0002 | 0/0 | 20 | 0 | 3 | 11 | 0 | 6 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0004 | 0/0 | 6 | 1 | 1 | 0 | 3 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0131 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0001c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0003c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0004c0005t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0005c0006t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0006c0008t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0007c0010t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0008c0009t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
a0009c0011t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0066 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00738 | hp2 | a0004 | c0005 | t0001 | g0018 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01069 | hp1 | a0004 | c0005 | t0001 | g0018 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0070 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01258 | hp2 | a0008 | c0009 | t0001 | g0113 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01928 | hp1 | a0009 | c0011 | t0001 | g0043 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02257 | hp1 | a0007 | c0010 | t0001 | g0180 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0023 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0024 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0024 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03540 | hp2 | a0005 | c0006 | t0002 | g0064 | AFR | GWD | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0067 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19043 | hp1 | a0001 | c0007 | t0001 | g0091 | AFR | LWK | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | YRI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ASW | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02109 | hp2 | a0006 | c0008 | t0001 | g0026 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0131 | REF | REF | TCTN1_chr12_110609129_110654430 | TCTN1 | chr12 | 110609129 | 110654430 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110614196
|
G | A | 1 | a0005 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.14G>A | p.Gly5Asp | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/15 | 68/2222 | 14/1779 | 5/592 | chr12 | 110614196 | ||
chr12:110614351
|
C | T | 1 | a0009 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.169C>T | p.Pro57Ser | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/15 | 223/2222 | 169/1779 | 57/592 | chr12 | 110614351 | ||
chr12:110642292
|
A | G | 1 | a0004 | 2 | HG00738.hp2 HG01069.hp1 |
missense_variant | MODERATE | c.1234A>G | p.Ile412Val | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/15 | 1288/2222 | 1234/1779 | 412/592 | chr12 | 110642292 | ||
chr12:110645014
|
G | C | 1 | a0003 | 2 | HG02976.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1379G>C | p.Ser460Thr | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/15 | 1433/2222 | 1379/1779 | 460/592 | chr12 | 110645014 | ||
chr12:110645022
|
T | C | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1387T>C | p.Trp463Arg | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/15 | 1441/2222 | 1387/1779 | 463/592 | chr12 | 110645022 | ||
chr12:110645031
|
G | T | 1 | a0002 | 5 | HG00735.hp2 HG01106.hp1 HG02735.hp1 others(2): Show |
missense_variant | MODERATE | c.1396G>T | p.Gly466Cys | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/15 | 1450/2222 | 1396/1779 | 466/592 | chr12 | 110645031 | ||
chr12:110645106
|
A | T | 1 | a0007 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1471A>T | p.Ile491Phe | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/15 | 1525/2222 | 1471/1779 | 491/592 | chr12 | 110645106 | ||
chr12:110647771
|
C | T | 1 | a0008 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1658C>T | p.Thr553Met | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/15 | 1712/2222 | 1658/1779 | 553/592 | chr12 | 110647771 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110614212
|
G | A | 1 | a0001c0007 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.30G>A | p.Leu10Leu | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/15 | 84/2222 | 30/1779 | 10/592 | chr12 | 110614212 | ||
chr12:110640433
|
C | T | 1 | a0001c0002 | 10 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
synonymous_variant | LOW | c.894C>T | p.Leu298Leu | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 8/15 | 948/2222 | 894/1779 | 298/592 | chr12 | 110640433 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110614137
|
G | C | 1 | a0005c0006t0002 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/15 | 46 | chr12 | 110614137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:110614414
|
G | C | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.220+12G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110614414 | ||||||
chr12:110614589
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220+187A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110614589 | ||||||
chr12:110614660
|
T | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(47): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.220+258T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110614660 | ||||||
chr12:110614866
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.220+464A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110614866 | ||||||
chr12:110615210
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.220+808G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615210 | ||||||
chr12:110615235
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0182a0001c0001t0001g0183 | 4 | HG00558.hp2 NA18947.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+833C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615235 | ||||||
chr12:110615308
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.220+906G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615308 | ||||||
chr12:110615333
|
A | C | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.220+931A>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615333 | ||||||
chr12:110615397
|
G | T | 1 | a0007c0010t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220+995G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615397 | ||||||
chr12:110615449
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.220+1047C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615449 | ||||||
chr12:110615511
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0068others(9): Show | 16 | HG00735.hp2 HG01106.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+1109C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615511 | ||||||
chr12:110615698
|
G | A | 2 | a0001c0001t0001g0076a0003c0004t0001g0024 | 3 | HG02630.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.220+1296G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110615698 | ||||||
chr12:110616194
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220+1792C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616194 | ||||||
chr12:110616257
|
T | A | 4 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0077others(1): Show | 7 | HG01168.hp1 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+1855T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616257 | ||||||
chr12:110616257
|
T | TA | 3 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0080 | 7 | HG00558.hp1 HG02523.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+1855_220+1856i others(3): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616257 | ||||||
chr12:110616367
|
T | G | 1 | a0007c0010t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220+1965T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616367 | ||||||
chr12:110616650
|
C | G | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0168others(11): Show | 16 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+2248C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616650 | ||||||
chr12:110616753
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 9 | HG01081.hp2 HG01943.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+2351G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616753 | ||||||
chr12:110616767
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220+2365T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616767 | ||||||
chr12:110616786
|
G | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0033others(37): Show | 50 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.220+2384G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616786 | ||||||
chr12:110616798
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220+2396C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616798 | ||||||
chr12:110616853
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.220+2451C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616853 | ||||||
chr12:110616996
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220+2594C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110616996 | ||||||
chr12:110617323
|
A | G | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0168others(11): Show | 16 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-2513A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110617323 | ||||||
chr12:110617345
|
AT | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0034others(15): Show | 22 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.221-2478delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110617345 | |||||
chr12:110617411
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.221-2425C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110617411 | ||||||
chr12:110617509
|
T | A | 1 | a0005c0006t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.221-2327T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110617509 | ||||||
chr12:110617620
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221-2216A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110617620 | ||||||
chr12:110618016
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0007c0010t0001g0180 | 3 | HG01099.hp2 HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.221-1820A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110618016 | ||||||
chr12:110618056
|
G | GT | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG02293.hp1 HG02293.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.221-1774dupT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110618056 | |||||
chr12:110618073
|
CT | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0033others(23): Show | 31 | HG01109.hp2 HG01167.hp1 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.221-1746delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110618073 | |||||
chr12:110618302
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.221-1534G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110618302 | ||||||
chr12:110618868
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.221-968C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110618868 | ||||||
chr12:110619003
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.221-833C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110619003 | ||||||
chr12:110619039
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.221-797G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110619039 | ||||||
chr12:110619180
|
AAAAT | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(21): Show | 30 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.221-640_221-637del others(4): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 110619180 | |||||
chr12:110619484
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.221-352G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110619484 | ||||||
chr12:110619556
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.221-280G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110619556 | ||||||
chr12:110619787
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 6 | HG01884.hp2 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-49C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 1/14 | chr12 | 110619787 | ||||||
chr12:110620002
|
G | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 10 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.341+46G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620002 | ||||||
chr12:110620050
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.341+94A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620050 | ||||||
chr12:110620091
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG00099.hp2 HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.341+135C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620091 | ||||||
chr12:110620145
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.341+189C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620145 | ||||||
chr12:110620269
|
A | G | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.341+313A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620269 | ||||||
chr12:110620277
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.341+321G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620277 | ||||||
chr12:110620668
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.341+712G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620668 | ||||||
chr12:110620810
|
C | CT | 30 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0032others(27): Show | 36 | HG00558.hp2 HG00733.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.341+872dupT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 110620810 | |||||
chr12:110620810
|
CT | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0027others(8): Show | 14 | HG00597.hp1 HG01123.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+872delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 110620810 | |||||
chr12:110620856
|
A | G | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.341+900A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110620856 | ||||||
chr12:110621207
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.341+1251G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621207 | ||||||
chr12:110621304
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341+1348A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621304 | ||||||
chr12:110621394
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0036 | 3 | HG01261.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.341+1438T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621394 | ||||||
chr12:110621414
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.341+1458G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621414 | ||||||
chr12:110621497
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.341+1541G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621497 | ||||||
chr12:110621554
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.341+1598C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621554 | ||||||
chr12:110621837
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.341+1881G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110621837 | ||||||
chr12:110622008
|
G | A | 1 | a0001c0007t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+2052G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622008 | ||||||
chr12:110622030
|
C | CA | 1 | a0001c0001t0001g0007 | 4 | HG02040.hp2 NA18949.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+2075dupA | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 110622030 | |||||
chr12:110622141
|
A | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0071others(13): Show | 18 | HG01081.hp2 HG01099.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.341+2185A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622141 | ||||||
chr12:110622144
|
T | A | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0013others(60): Show | 83 | HG00323.hp1 HG01071.hp2 HG01081.hp1 others(80): Show |
intron_variant | MODIFIER | c.341+2188T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622144 | ||||||
chr12:110622147
|
T | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 19 | HG00738.hp2 HG01069.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.341+2191T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622147 | ||||||
chr12:110622150
|
T | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.341+2194T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622150 | ||||||
chr12:110622231
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341+2275C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622231 | ||||||
chr12:110622295
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.341+2339T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622295 | ||||||
chr12:110622428
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.341+2472G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622428 | ||||||
chr12:110622465
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341+2509C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622465 | ||||||
chr12:110622628
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.341+2672G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622628 | ||||||
chr12:110622868
|
G | C | 1 | a0001c0007t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341+2912G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110622868 | ||||||
chr12:110623059
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.341+3103G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623059 | ||||||
chr12:110623070
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0144 | 2 | NA18941.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.341+3114C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623070 | ||||||
chr12:110623205
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.342-3157A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623205 | ||||||
chr12:110623384
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.342-2978G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623384 | ||||||
chr12:110623484
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2878G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623484 | ||||||
chr12:110623565
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2797T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623565 | ||||||
chr12:110623629
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2733A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623629 | ||||||
chr12:110623680
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2682C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623680 | ||||||
chr12:110623682
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2680G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623682 | ||||||
chr12:110623695
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2667C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623695 | ||||||
chr12:110623713
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2649C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623713 | ||||||
chr12:110623742
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2620G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623742 | ||||||
chr12:110623747
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.342-2615C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623747 | ||||||
chr12:110623847
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 39 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.342-2515A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623847 | ||||||
chr12:110623880
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.342-2482T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623880 | ||||||
chr12:110623906
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342-2456T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623906 | ||||||
chr12:110623942
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.342-2420A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110623942 | ||||||
chr12:110624225
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.342-2137A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624225 | ||||||
chr12:110624292
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.342-2070T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624292 | ||||||
chr12:110624421
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.342-1941C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624421 | ||||||
chr12:110624599
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.342-1763T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624599 | ||||||
chr12:110624735
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(23): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.342-1627G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624735 | ||||||
chr12:110624847
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0128 | 4 | HG02717.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-1515G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624847 | ||||||
chr12:110624893
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.342-1469C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624893 | ||||||
chr12:110624917
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.342-1445C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624917 | ||||||
chr12:110624955
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.342-1407A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110624955 | ||||||
chr12:110625047
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(99): Show | 132 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.342-1315C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625047 | ||||||
chr12:110625094
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.342-1268G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625094 | ||||||
chr12:110625277
|
T | G | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.342-1085T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625277 | ||||||
chr12:110625372
|
C | T | 6 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0077others(3): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.342-990C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625372 | ||||||
chr12:110625638
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.342-724G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625638 | ||||||
chr12:110625756
|
AT | A | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(30): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.342-590delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 110625756 | |||||
chr12:110625995
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.342-367G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110625995 | ||||||
chr12:110626093
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.342-269C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110626093 | ||||||
chr12:110626252
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.342-110C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 2/14 | chr12 | 110626252 | ||||||
chr12:110626588
|
T | C | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.472+96T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626588 | ||||||
chr12:110626648
|
C | T | 1 | a0002c0003t0001g0070 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.472+156C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626648 | ||||||
chr12:110626654
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.472+162A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626654 | ||||||
chr12:110626763
|
G | GT | 54 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0022others(51): Show | 66 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.472+295dupT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110626763 | |||||
chr12:110626775
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.472+283T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626775 | ||||||
chr12:110626800
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+308C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626800 | ||||||
chr12:110626801
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 13 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.472+309G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110626801 | ||||||
chr12:110627084
|
T | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.472+592T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627084 | ||||||
chr12:110627098
|
C | CT | 9 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0083others(6): Show | 9 | HG01358.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.472+623dupT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110627098 | |||||
chr12:110627098
|
CT | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0033a0001c0001t0001g0034others(14): Show | 21 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.472+623delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110627098 | |||||
chr12:110627102
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.472+610T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627102 | ||||||
chr12:110627304
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472+812C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627304 | ||||||
chr12:110627364
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0068others(9): Show | 16 | HG00735.hp2 HG01106.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+872C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627364 | ||||||
chr12:110627607
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.472+1115T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627607 | ||||||
chr12:110627953
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.473-814A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110627953 | ||||||
chr12:110628050
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.473-717A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110628050 | ||||||
chr12:110628075
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.473-692C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110628075 | ||||||
chr12:110628190
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0136 | 2 | HG00280.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.473-577C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110628190 | ||||||
chr12:110628191
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.473-576G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110628191 | ||||||
chr12:110628341
|
CT | C | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0147others(13): Show | 18 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.473-409delT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110628341 | |||||
chr12:110628757
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 9 | HG01081.hp2 HG01943.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-10T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | chr12 | 110628757 | ||||||
chr12:110628757
|
TAAA | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0009c0011t0001g0043 | 3 | HG01123.hp1 HG01928.hp1 HG01952.hp1 |
splice_region_variant&intron_variant | LOW | c.473-6_473-4delAAA | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 110628757 | |||||
chr12:110629193
|
A | G | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.624+275A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629193 | ||||||
chr12:110629253
|
AATTAAAC others(61): Show |
A | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.624+336_624+403del others(68): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629253 | ||||||
chr12:110629305
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0112a0001c0001t0001g0164 | 5 | HG01071.hp2 HG01081.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+387G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629305 | ||||||
chr12:110629309
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624+391G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629309 | ||||||
chr12:110629346
|
A | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 9 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.624+428A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629346 | ||||||
chr12:110629447
|
C | G | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.624+529C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629447 | ||||||
chr12:110629569
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.624+651C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629569 | ||||||
chr12:110629646
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG01891.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.624+728G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629646 | ||||||
chr12:110629945
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.624+1027A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629945 | ||||||
chr12:110629989
|
C | A | 1 | a0008c0009t0001g0113 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.624+1071C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629989 | ||||||
chr12:110629989
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.624+1071C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110629989 | ||||||
chr12:110630087
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0054 | 3 | HG03516.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624+1169A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630087 | ||||||
chr12:110630291
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(28): Show | 38 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.624+1373C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630291 | ||||||
chr12:110630584
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0142 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.624+1666A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630584 | ||||||
chr12:110630831
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.625-1641C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630831 | ||||||
chr12:110630865
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.625-1607C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630865 | ||||||
chr12:110630868
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.625-1604C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110630868 | ||||||
chr12:110631300
|
C | CA | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.625-1172_625-1171i others(3): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110631300 | ||||||
chr12:110631325
|
T | C | 6 | a0001c0002t0001g0011a0001c0002t0001g0025a0001c0002t0001g0077others(3): Show | 9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-1147T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110631325 | ||||||
chr12:110631836
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.625-636A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110631836 | ||||||
chr12:110632019
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 9 | HG01167.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-453A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110632019 | ||||||
chr12:110632202
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.625-270C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110632202 | ||||||
chr12:110632364
|
G | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 40 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.625-108G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 4/14 | chr12 | 110632364 | ||||||
chr12:110632744
|
C | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(13): Show | 21 | HG00558.hp2 HG01884.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.712+185C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110632744 | ||||||
chr12:110632765
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0041a0009c0011t0001g0043 | 3 | HG01123.hp1 HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.712+206G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110632765 | ||||||
chr12:110632995
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.712+436C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110632995 | ||||||
chr12:110633258
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.712+699A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633258 | ||||||
chr12:110633321
|
T | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0062others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+762T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633321 | ||||||
chr12:110633330
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.712+771G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633330 | ||||||
chr12:110633374
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.712+815G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633374 | ||||||
chr12:110633544
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.712+985G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633544 | ||||||
chr12:110633676
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.713-994C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633676 | ||||||
chr12:110633743
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.713-927C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633743 | ||||||
chr12:110633831
|
T | C | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.713-839T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110633831 | ||||||
chr12:110634214
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.713-456T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110634214 | ||||||
chr12:110634448
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.713-222G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110634448 | ||||||
chr12:110634595
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.713-75T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 5/14 | chr12 | 110634595 | ||||||
chr12:110634836
|
G | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.822+57G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110634836 | ||||||
chr12:110634847
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+68A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110634847 | ||||||
chr12:110635014
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0001g0128 | 4 | HG02717.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+235T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635014 | ||||||
chr12:110635015
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.822+236A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635015 | ||||||
chr12:110635393
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0106 | 3 | HG02717.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.822+614C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635393 | ||||||
chr12:110635422
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.822+643C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635422 | ||||||
chr12:110635442
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 9 | HG01081.hp2 HG01943.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.822+663C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635442 | ||||||
chr12:110635457
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0134 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.822+678A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635457 | ||||||
chr12:110635461
|
T | A | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.822+682T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635461 | ||||||
chr12:110635471
|
C | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0033others(37): Show | 50 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.822+692C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635471 | ||||||
chr12:110635550
|
G | GGCTGAGG others(9): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0045others(1): Show | 6 | NA18962.hp1 NA18983.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+791_822+806dup others(16): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 110635550 | |||||
chr12:110635632
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.823-849G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635632 | ||||||
chr12:110635668
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.823-813G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635668 | ||||||
chr12:110635720
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0159a0001c0001t0001g0181 | 3 | HG01346.hp1 HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.823-761A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635720 | ||||||
chr12:110635800
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823-681C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110635800 | ||||||
chr12:110636208
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.823-273T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110636208 | ||||||
chr12:110636475
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG01167.hp2 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.823-6A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 6/14 | chr12 | 110636475 | ||||||
chr12:110636777
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.843+276T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110636777 | ||||||
chr12:110636795
|
C | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0156 | 3 | HG01099.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.843+294C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110636795 | ||||||
chr12:110636898
|
A | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(30): Show | 43 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.843+397A>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110636898 | ||||||
chr12:110637045
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.843+544G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110637045 | ||||||
chr12:110637199
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.843+698C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110637199 | ||||||
chr12:110637432
|
C | T | 1 | a0001c0001t0001g0007 | 4 | HG02040.hp2 NA18949.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+931C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110637432 | ||||||
chr12:110637665
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.843+1164T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110637665 | ||||||
chr12:110638018
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(29): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.843+1517C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638018 | ||||||
chr12:110638102
|
C | CT | 33 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(30): Show | 41 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.843+1602dupT | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 110638102 | |||||
chr12:110638550
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.844-1833G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638550 | ||||||
chr12:110638605
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.844-1778C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638605 | ||||||
chr12:110638692
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0157others(1): Show | 4 | HG01099.hp2 HG02145.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-1691T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638692 | ||||||
chr12:110638867
|
A | G | 1 | a0002c0003t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-1516A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638867 | ||||||
chr12:110638947
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.844-1436G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110638947 | ||||||
chr12:110639145
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.844-1238G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110639145 | ||||||
chr12:110639176
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0056others(1): Show | 5 | HG02647.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1207T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110639176 | ||||||
chr12:110639438
|
C | CTG | 7 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0119others(4): Show | 9 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-923_844-922dup others(2): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 110639438 | |||||
chr12:110639490
|
A | G | 1 | a0002c0003t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.844-893A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110639490 | ||||||
chr12:110639706
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.844-677A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110639706 | ||||||
chr12:110639903
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.844-480G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110639903 | ||||||
chr12:110640092
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0050 | 3 | HG01167.hp2 HG01169.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.844-291T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 7/14 | chr12 | 110640092 | ||||||
chr12:110640576
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+59G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 8/14 | chr12 | 110640576 | ||||||
chr12:110640598
|
C | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 8 | HG01099.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+81C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 8/14 | chr12 | 110640598 | ||||||
chr12:110641210
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1104+61C>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 9/14 | chr12 | 110641210 | ||||||
chr12:110641218
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1104+69A>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 9/14 | chr12 | 110641218 | ||||||
chr12:110641384
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1105-158C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 9/14 | chr12 | 110641384 | ||||||
chr12:110641387
|
C | CTTACTGT others(24): Show |
1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1105-155_1105-154i others(33): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 9/14 | chr12 | 110641387 | ||||||
chr12:110641399
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1105-143G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 9/14 | chr12 | 110641399 | ||||||
chr12:110641672
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1190+45A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 10/14 | chr12 | 110641672 | ||||||
chr12:110641990
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0184a0003c0004t0001g0024 | 4 | HG02630.hp2 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1191-259C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 10/14 | chr12 | 110641990 | ||||||
chr12:110642052
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1191-197T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 10/14 | chr12 | 110642052 | ||||||
chr12:110642180
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1191-69A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 10/14 | chr12 | 110642180 | ||||||
chr12:110642695
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1331+306G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110642695 | ||||||
chr12:110642710
|
G | C | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1331+321G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110642710 | ||||||
chr12:110643225
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1331+836G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110643225 | ||||||
chr12:110643363
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1331+974A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110643363 | ||||||
chr12:110643392
|
A | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0033others(37): Show | 50 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1331+1003A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110643392 | ||||||
chr12:110643744
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0109a0001c0001t0001g0120others(1): Show | 6 | HG00099.hp1 HG00280.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332-1223G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110643744 | ||||||
chr12:110643793
|
C | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0168others(11): Show | 16 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1332-1174C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110643793 | ||||||
chr12:110644085
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1332-882G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644085 | ||||||
chr12:110644205
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0153a0001c0001t0001g0155 | 4 | HG01884.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-762C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644205 | ||||||
chr12:110644229
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1332-738T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644229 | ||||||
chr12:110644293
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1332-674A>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644293 | ||||||
chr12:110644337
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0027others(23): Show | 35 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1332-630C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644337 | ||||||
chr12:110644389
|
C | G | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1332-578C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644389 | ||||||
chr12:110644609
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1332-358C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644609 | ||||||
chr12:110644858
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1332-109C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644858 | ||||||
chr12:110644879
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1332-88C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644879 | ||||||
chr12:110644932
|
G | C | 1 | a0001c0002t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1332-35G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 11/14 | chr12 | 110644932 | ||||||
chr12:110645198
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1494+69C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110645198 | ||||||
chr12:110645279
|
G | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(30): Show | 43 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1494+150G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110645279 | ||||||
chr12:110645649
|
C | T | 1 | a0002c0003t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1494+520C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110645649 | ||||||
chr12:110645753
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1494+624G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110645753 | ||||||
chr12:110645935
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 8 | HG01081.hp2 HG01943.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1494+806C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110645935 | ||||||
chr12:110646002
|
C | T | 1 | a0005c0006t0002g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1494+873C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646002 | ||||||
chr12:110646048
|
C | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 14 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+919C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646048 | ||||||
chr12:110646163
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1495-1033A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646163 | ||||||
chr12:110646175
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(21): Show | 30 | HG00323.hp1 HG01167.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1495-1021G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646175 | ||||||
chr12:110646277
|
A | AGTCTGCA others(315): Show |
1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1495-904_1495-903i others(324): Show |
TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 110646277 | |||||
chr12:110646322
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1495-874C>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646322 | ||||||
chr12:110646349
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1495-847T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646349 | ||||||
chr12:110646354
|
G | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1495-842G>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646354 | ||||||
chr12:110646503
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1495-693C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646503 | ||||||
chr12:110646712
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1495-484T>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646712 | ||||||
chr12:110646735
|
G | A | 32 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 40 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1495-461G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646735 | ||||||
chr12:110646879
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0143 | 6 | HG02165.hp2 NA18946.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495-317G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646879 | ||||||
chr12:110646956
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1495-240C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 12/14 | chr12 | 110646956 | ||||||
chr12:110647382
|
G | C | 1 | a0001c0001t0001g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1635+46G>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 13/14 | chr12 | 110647382 | ||||||
chr12:110647501
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1635+165C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 13/14 | chr12 | 110647501 | ||||||
chr12:110647525
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1635+189T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 13/14 | chr12 | 110647525 | ||||||
chr12:110647563
|
C | T | 4 | a0002c0003t0001g0023a0002c0003t0001g0066a0002c0003t0001g0067others(1): Show | 5 | HG00735.hp2 HG01106.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1636-186C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 13/14 | chr12 | 110647563 | ||||||
chr12:110648075
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 40 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.*1+182A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648075 | ||||||
chr12:110648119
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*1+226C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648119 | ||||||
chr12:110648158
|
A | C | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.*1+265A>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648158 | ||||||
chr12:110648180
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(30): Show | 43 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.*1+287A>G | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648180 | ||||||
chr12:110648428
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 5 | HG02559.hp2 HG03225.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.*1+535T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648428 | ||||||
chr12:110648440
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.*1+547T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648440 | ||||||
chr12:110648594
|
A | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0125a0001c0001t0001g0144 | 3 | NA18941.hp2 NA18971.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.*2-449A>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648594 | ||||||
chr12:110648621
|
C | T | 1 | a0004c0005t0001g0018 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.*2-422C>T | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648621 | ||||||
chr12:110648644
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0034others(28): Show | 38 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.*2-399T>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648644 | ||||||
chr12:110648788
|
AAG | A | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0168others(11): Show | 16 | HG00323.hp1 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.*2-248_*2-247delAG | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 110648788 | |||||
chr12:110648825
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*2-218T>C | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648825 | ||||||
chr12:110648960
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.*2-83G>A | TCTN1 | ENSG00000204852.17 | transcript | ENST00000397659.9 | protein_coding | 14/14 | chr12 | 110648960 |