geneid | 23424 |
---|---|
ensemblid | ENSG00000196116.8 |
hgncid | 30831 |
symbol | TDRD7 |
name | tudor domain containing 7 |
refseq_nuc | NM_014290.3 |
refseq_prot | NP_055105.2 |
ensembl_nuc | ENST00000355295.5 |
ensembl_prot | ENSP00000347444.4 |
mane_status | MANE Select |
chr | chr9 |
start | 97412096 |
end | 97496125 |
strand | + |
ver | v1.2 |
region | chr9:97412096-97496125 |
region5000 | chr9:97407096-97501125 |
regionname0 | TDRD7_chr9_97412096_97496125 |
regionname5000 | TDRD7_chr9_97407096_97501125 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1098 | 193 | 49 | 38 | 84 | 2 | 20 | 63 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002 | 1/1 | 1098 | 155 | 32 | 31 | 68 | 4 | 18 | 51 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0003 | 0/0 | 1098 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0004 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0005 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0006 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0008 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3297 | 156 | 35 | 35 | 67 | 2 | 17 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0002 | 1/1 | 3297 | 152 | 32 | 31 | 66 | 3 | 18 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0003 | 0/0 | 3297 | 18 | 1 | 0 | 16 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0004 | 0/0 | 3297 | 12 | 7 | 3 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0005 | 0/0 | 3297 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0006 | 0/0 | 3297 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0007 | 0/0 | 3297 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0008 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0009 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0010 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0011 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0012 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0013 | 0/0 | 3297 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0014 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0015 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
c0016 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 392 | 334 | 83 | 66 | 139 | 6 | 38 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
t0002 | 0/0 | 392 | 14 | 2 | 4 | 8 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
t0003 | 0/0 | 392 | 7 | 0 | 0 | 7 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
t0004 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3297 | 156 | 35 | 35 | 67 | 2 | 17 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0003 | 0/0 | 3297 | 18 | 1 | 0 | 16 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0004 | 0/0 | 3297 | 12 | 7 | 3 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0005 | 0/0 | 3297 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0009 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0010 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0015 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0002 | 1/1 | 3297 | 152 | 32 | 31 | 66 | 3 | 18 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0007 | 0/0 | 3297 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0008 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0003c0006 | 0/0 | 3297 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0004c0016 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0005c0013 | 0/0 | 3297 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0006c0011 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0007c0014 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0008c0012 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3688 | 154 | 35 | 35 | 65 | 2 | 17 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0001t0002 | 0/0 | 3688 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0003t0001 | 0/0 | 3688 | 18 | 1 | 0 | 16 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0004t0001 | 0/0 | 3688 | 12 | 7 | 3 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0005t0001 | 0/0 | 3688 | 4 | 4 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0009t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0010t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0001c0015t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0002t0001 | 1/1 | 3688 | 132 | 29 | 27 | 53 | 3 | 18 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0002t0002 | 0/0 | 3688 | 12 | 2 | 4 | 6 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0002t0003 | 0/0 | 3688 | 7 | 0 | 0 | 7 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0002t0004 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0007t0001 | 0/0 | 3688 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0002c0008t0001 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0003c0006t0001 | 0/0 | 3688 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0004c0016t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0005c0013t0001 | 0/0 | 3688 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0006c0011t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0007c0014t0001 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
a0008c0012t0001 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | copy fasta | chr9 | 97407096 | 97501125 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0005t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0005t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0009t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0010t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0001c0015t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0002t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0007t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0002c0008t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0003c0006t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0003c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0004c0016t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0005c0013t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0006c0011t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0007c0014t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
a0008c0012t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0002 | c0008 | t0001 | g0021 | EUR | FIN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | FIN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0036 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0303 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0103 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01070 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0305 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0226 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0210 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | KHV | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0112 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CDX | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02273 | hp2 | a0005 | c0013 | t0001 | g0244 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0110 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0105 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0320 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02630 | hp2 | a0006 | c0011 | t0001 | g0025 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0314 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0200 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0312 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0319 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02976 | hp1 | a0003 | c0006 | t0001 | g0030 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03017 | hp2 | a0001 | c0004 | t0001 | g0104 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0307 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03225 | hp1 | a0007 | c0014 | t0001 | g0111 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0318 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03453 | hp2 | a0001 | c0009 | t0001 | g0323 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0313 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03579 | hp1 | a0003 | c0006 | t0001 | g0005 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0144 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0309 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0203 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0034 | SAS | BEB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0310 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0102 | SAS | STU | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18951 | hp2 | a0002 | c0007 | t0001 | g0011 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18974 | hp2 | a0002 | c0002 | t0003 | g0233 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18977 | hp1 | a0001 | c0003 | t0001 | g0311 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19005 | hp2 | a0001 | c0010 | t0001 | g0296 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0317 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19030 | hp2 | a0001 | c0015 | t0001 | g0024 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19055 | hp2 | a0004 | c0016 | t0001 | g0281 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19056 | hp2 | a0002 | c0002 | t0003 | g0204 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19077 | hp2 | a0002 | c0007 | t0001 | g0011 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19078 | hp2 | a0002 | c0002 | t0003 | g0232 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19084 | hp1 | a0008 | c0012 | t0001 | g0076 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19085 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19086 | hp2 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19087 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20129 | hp1 | a0003 | c0006 | t0001 | g0005 | AFR | ASW | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ASW | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | GIH | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | GIH | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0316 | AFR | MSL | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | LWK | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0222 | REF | REF | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0150 | REF | REF | TDRD7_chr9_97407096_97501125 | TDRD7 | chr9 | 97407096 | 97501125 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97432066
|
A | G | 1 | a0004 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.391A>G | p.Asn131Asp | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 540/3688 | 391/3297 | 131/1098 | chr9 | 97432066 | ||
chr9:97432112
|
A | G | 1 | a0003 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.437A>G | p.Lys146Arg | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 586/3688 | 437/3297 | 146/1098 | chr9 | 97432112 | ||
chr9:97432124
|
T | C | 7 | a0001a0003a0004others(4): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
missense_variant | MODERATE | c.449T>C | p.Val150Ala | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 598/3688 | 449/3297 | 150/1098 | chr9 | 97432124 | ||
chr9:97460535
|
A | G | 1 | a0005 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1213A>G | p.Lys405Glu | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1362/3688 | 1213/3297 | 405/1098 | chr9 | 97460535 | ||
chr9:97460557
|
A | C | 1 | a0008 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1235A>C | p.Lys412Thr | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1384/3688 | 1235/3297 | 412/1098 | chr9 | 97460557 | ||
chr9:97480864
|
A | G | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2338A>G | p.Ile780Val | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/17 | 2487/3688 | 2338/3297 | 780/1098 | chr9 | 97480864 | ||
chr9:97482879
|
G | A | 1 | a0006 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2443G>A | p.Ala815Thr | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/17 | 2592/3688 | 2443/3297 | 815/1098 | chr9 | 97482879 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97428498
|
A | G | 14 | a0001c0001a0001c0003a0001c0004others(11): Show | 203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
synonymous_variant | LOW | c.33A>G | p.Leu11Leu | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/17 | 182/3688 | 33/3297 | 11/1098 | chr9 | 97428498 | ||
chr9:97432218
|
G | A | 1 | a0001c0009 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.543G>A | p.Val181Val | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/17 | 692/3688 | 543/3297 | 181/1098 | chr9 | 97432218 | ||
chr9:97439260
|
G | A | 1 | a0001c0010 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.579G>A | p.Ala193Ala | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/17 | 728/3688 | 579/3297 | 193/1098 | chr9 | 97439260 | ||
chr9:97439269
|
A | G | 5 | a0001c0003a0001c0004a0001c0005others(2): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
synonymous_variant | LOW | c.588A>G | p.Gln196Gln | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/17 | 737/3688 | 588/3297 | 196/1098 | chr9 | 97439269 | ||
chr9:97460234
|
G | A | 1 | a0001c0005 | 4 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.912G>A | p.Lys304Lys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/17 | 1061/3688 | 912/3297 | 304/1098 | chr9 | 97460234 | ||
chr9:97472351
|
T | C | 1 | a0002c0008 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.1800T>C | p.Cys600Cys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 1949/3688 | 1800/3297 | 600/1098 | chr9 | 97472351 | ||
chr9:97472420
|
A | G | 1 | a0001c0015 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1869A>G | p.Ser623Ser | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 2018/3688 | 1869/3297 | 623/1098 | chr9 | 97472420 | ||
chr9:97472474
|
G | A | 3 | a0001c0004a0001c0005a0007c0014 | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
synonymous_variant | LOW | c.1923G>A | p.Lys641Lys | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/17 | 2072/3688 | 1923/3297 | 641/1098 | chr9 | 97472474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97412112
|
C | G | 3 | a0001c0001t0002a0002c0002t0002a0002c0002t0003 | 21 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-133C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16354 | chr9 | 97412112 | |||||
chr9:97412162
|
G | C | 1 | a0002c0002t0003 | 7 | NA18941.hp2 NA18974.hp2 NA19056.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-83G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16304 | chr9 | 97412162 | |||||
chr9:97412198
|
G | A | 1 | a0002c0002t0004 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/17 | 16268 | chr9 | 97412198 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97412361
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-7+123A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412361 | ||||||
chr9:97412376
|
T | C | 1 | a0002c0008t0001g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-7+138T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412376 | ||||||
chr9:97412413
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-7+175C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412413 | ||||||
chr9:97412492
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+254G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412492 | ||||||
chr9:97412535
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-7+297C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412535 | ||||||
chr9:97412585
|
C | T | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+347C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412585 | ||||||
chr9:97412661
|
C | G | 1 | a0002c0002t0002g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-7+423C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412661 | ||||||
chr9:97412789
|
G | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0003t0001g0026others(22): Show | 26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+551G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412789 | ||||||
chr9:97412934
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-7+696A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97412934 | ||||||
chr9:97413066
|
C | A | 25 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0003t0001g0026others(22): Show | 26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+828C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413066 | ||||||
chr9:97413110
|
G | A | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 75 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.-7+872G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413110 | ||||||
chr9:97413121
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7+883C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413121 | ||||||
chr9:97413130
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+892A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413130 | ||||||
chr9:97413196
|
G | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 104 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.-7+958G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413196 | ||||||
chr9:97413369
|
T | G | 4 | a0001c0003t0001g0026a0001c0009t0001g0323a0001c0015t0001g0024others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+1131T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413369 | ||||||
chr9:97413414
|
T | TTA | 25 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0003t0001g0026others(22): Show | 26 | HG00408.hp1 HG00558.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7+1177_-7+1178dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97413414 | |||||
chr9:97413436
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-7+1198G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413436 | ||||||
chr9:97413760
|
G | A | 1 | a0002c0002t0001g0113 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-7+1522G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413760 | ||||||
chr9:97413801
|
C | G | 3 | a0001c0003t0001g0026a0001c0009t0001g0323a0006c0011t0001g0025 | 3 | HG01891.hp2 HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7+1563C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97413801 | ||||||
chr9:97414336
|
T | G | 1 | a0002c0002t0002g0114 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+2098T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414336 | ||||||
chr9:97414652
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7+2414G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414652 | ||||||
chr9:97414719
|
C | A | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+2481C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414719 | ||||||
chr9:97414779
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-7+2541T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414779 | ||||||
chr9:97414835
|
T | G | 3 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0118 | 3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-7+2597T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414835 | ||||||
chr9:97414936
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7+2698G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414936 | ||||||
chr9:97414948
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+2710C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97414948 | ||||||
chr9:97415188
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-7+2950A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415188 | ||||||
chr9:97415250
|
G | A | 1 | a0001c0004t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-7+3012G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415250 | ||||||
chr9:97415275
|
G | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+3037G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415275 | ||||||
chr9:97415327
|
T | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+3089T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415327 | ||||||
chr9:97415395
|
C | T | 1 | a0002c0002t0001g0310 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7+3157C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415395 | ||||||
chr9:97415429
|
G | T | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+3191G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415429 | ||||||
chr9:97415719
|
G | T | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+3481G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415719 | ||||||
chr9:97415734
|
A | G | 1 | a0002c0002t0001g0309 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-7+3496A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415734 | ||||||
chr9:97415759
|
C | T | 8 | a0001c0004t0001g0112a0001c0004t0001g0315a0001c0004t0001g0316others(5): Show | 8 | HG02145.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3521C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415759 | ||||||
chr9:97415971
|
C | T | 278 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(275): Show | 299 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.-7+3733C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97415971 | ||||||
chr9:97416196
|
T | C | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+3958T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416196 | ||||||
chr9:97416213
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | NA18948.hp1 NA18999.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-7+3975T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416213 | ||||||
chr9:97416235
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-7+3997C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416235 | ||||||
chr9:97416562
|
G | A | 1 | a0002c0002t0002g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-7+4324G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416562 | ||||||
chr9:97416669
|
A | C | 1 | a0002c0002t0001g0308 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7+4431A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416669 | ||||||
chr9:97416794
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-7+4556G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416794 | ||||||
chr9:97416853
|
C | T | 1 | a0002c0002t0002g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7+4615C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416853 | ||||||
chr9:97416867
|
A | G | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4629A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416867 | ||||||
chr9:97416885
|
A | C | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-7+4647A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97416885 | ||||||
chr9:97417016
|
A | G | 3 | a0002c0002t0001g0304a0002c0002t0001g0305a0002c0002t0001g0306 | 3 | HG01256.hp2 HG02486.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-7+4778A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417016 | ||||||
chr9:97417062
|
C | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4824C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417062 | ||||||
chr9:97417063
|
G | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+4825G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417063 | ||||||
chr9:97417427
|
G | A | 6 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0317others(3): Show | 6 | HG02615.hp1 HG02895.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+5189G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417427 | ||||||
chr9:97417559
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-7+5321A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417559 | ||||||
chr9:97417701
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-7+5463C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417701 | ||||||
chr9:97417846
|
G | A | 3 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0172 | 3 | HG00597.hp2 NA19077.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-7+5608G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417846 | ||||||
chr9:97417936
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-7+5698C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97417936 | ||||||
chr9:97418047
|
C | T | 2 | a0002c0002t0001g0020a0002c0002t0004g0110 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+5809C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418047 | ||||||
chr9:97418090
|
C | A | 8 | a0002c0002t0001g0174a0002c0002t0001g0175a0002c0002t0001g0176others(5): Show | 8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+5852C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418090 | ||||||
chr9:97418273
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-7+6035A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418273 | ||||||
chr9:97418529
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-7+6291T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418529 | ||||||
chr9:97418539
|
TA | T | 19 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(16): Show | 20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7+6312delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97418539 | |||||
chr9:97418633
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-7+6395G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418633 | ||||||
chr9:97418686
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+6448G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418686 | ||||||
chr9:97418702
|
A | G | 1 | a0002c0002t0002g0114 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+6464A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418702 | ||||||
chr9:97418752
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+6514C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418752 | ||||||
chr9:97418787
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+6549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418787 | ||||||
chr9:97418814
|
C | T | 1 | a0002c0002t0002g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7+6576C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418814 | ||||||
chr9:97418867
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-7+6629G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418867 | ||||||
chr9:97418999
|
A | T | 1 | a0002c0007t0001g0011 | 2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-7+6761A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97418999 | ||||||
chr9:97419119
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-7+6881A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419119 | ||||||
chr9:97419253
|
A | AGAGCACA others(15): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18969.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-7+7019_-7+7040dup others(22): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97419253 | |||||
chr9:97419371
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+7133C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419371 | ||||||
chr9:97419438
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0302 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-7+7200A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419438 | ||||||
chr9:97419487
|
C | G | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7249C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419487 | ||||||
chr9:97419537
|
C | T | 1 | a0001c0003t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+7299C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419537 | ||||||
chr9:97419576
|
A | G | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7338A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419576 | ||||||
chr9:97419707
|
T | C | 2 | a0001c0001t0001g0027a0001c0009t0001g0323 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+7469T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419707 | ||||||
chr9:97419823
|
A | C | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7+7585A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97419823 | ||||||
chr9:97420047
|
G | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-7+7809G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420047 | ||||||
chr9:97420164
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-7+7926C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420164 | ||||||
chr9:97420268
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7+8030A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420268 | ||||||
chr9:97420278
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7+8040T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420278 | ||||||
chr9:97420364
|
T | G | 3 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0118 | 3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-6-8096T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420364 | ||||||
chr9:97420364
|
TG | T | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 82 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-6-8088delG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97420364 | |||||
chr9:97420502
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-6-7958G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420502 | ||||||
chr9:97420556
|
A | T | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-7904A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420556 | ||||||
chr9:97420658
|
T | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7802T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420658 | ||||||
chr9:97420878
|
A | G | 4 | a0002c0002t0001g0159a0002c0002t0001g0160a0002c0002t0001g0161others(1): Show | 4 | NA18953.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-7582A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420878 | ||||||
chr9:97420903
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-7557C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420903 | ||||||
chr9:97420970
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7490C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420970 | ||||||
chr9:97420995
|
C | T | 18 | a0001c0001t0001g0300a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.-6-7465C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97420995 | ||||||
chr9:97421003
|
T | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-7457T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421003 | ||||||
chr9:97421004
|
G | A | 3 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0317 | 3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-7456G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421004 | ||||||
chr9:97421014
|
A | G | 1 | a0001c0005t0001g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6-7446A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421014 | ||||||
chr9:97421134
|
CA | C | 38 | a0001c0001t0001g0299a0001c0003t0001g0026a0001c0003t0001g0031others(35): Show | 39 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-6-7309delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421134 | |||||
chr9:97421151
|
AG | A | 6 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(3): Show | 6 | HG02615.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-7308delG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421151 | ||||||
chr9:97421216
|
A | G | 1 | a0002c0002t0001g0310 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-6-7244A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421216 | ||||||
chr9:97421300
|
A | G | 1 | a0001c0005t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-6-7160A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421300 | ||||||
chr9:97421359
|
T | C | 1 | a0001c0001t0001g0009 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-6-7101T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421359 | ||||||
chr9:97421668
|
A | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-6-6792A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421668 | ||||||
chr9:97421679
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-6781G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421679 | ||||||
chr9:97421697
|
TTTGTGTG others(6): Show |
T | 1 | a0002c0002t0001g0186 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-6-6761_-6-6749del others(13): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421697 | |||||
chr9:97421697
|
TTTGTGTG others(8): Show |
T | 1 | a0002c0002t0001g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-6-6761_-6-6747del others(15): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421697 | |||||
chr9:97421698
|
T | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0002c0002t0001g0184 | 3 | HG00639.hp2 HG02970.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-6-6762T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421698 | ||||||
chr9:97421698
|
T | TTG | 13 | a0001c0001t0001g0047a0002c0002t0001g0053a0002c0002t0001g0054others(10): Show | 13 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-6717_-6-6716dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
T | TTGTG | 4 | a0002c0002t0001g0020a0002c0002t0001g0056a0002c0002t0001g0158others(1): Show | 5 | HG01891.hp1 HG02976.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-6719_-6-6716dup others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTG | T | 49 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0090others(46): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-6-6717_-6-6716del others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTG | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(126): Show | 152 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.-6-6719_-6-6716del others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTGTG | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 17 | HG00741.hp1 HG01975.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6-6721_-6-6716del others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0003t0001g0026others(1): Show | 4 | HG01891.hp2 HG02300.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-6723_-6-6716del others(8): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0004t0001g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-6-6725_-6-6716del others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTGTGT others(7): Show |
T | 7 | a0002c0002t0001g0118a0002c0002t0001g0215a0002c0002t0001g0216others(4): Show | 7 | HG01256.hp2 HG01358.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-6729_-6-6716del others(14): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421698
|
TTGTGTGT others(9): Show |
T | 51 | a0001c0001t0001g0027a0001c0001t0001g0241a0002c0002t0001g0022others(48): Show | 54 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-6-6731_-6-6716del others(16): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97421698 | |||||
chr9:97421699
|
TGTGTGTG others(8): Show |
T | 1 | a0002c0002t0003g0232 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-6-6760_-6-6746del others(15): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421699 | ||||||
chr9:97421810
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-6-6650C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421810 | ||||||
chr9:97421845
|
A | G | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-6615A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421845 | ||||||
chr9:97421955
|
C | G | 1 | a0002c0002t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-6-6505C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97421955 | ||||||
chr9:97422118
|
G | A | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-6342G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422118 | ||||||
chr9:97422395
|
C | CA | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-6054dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97422395 | |||||
chr9:97422449
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6-6011G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422449 | ||||||
chr9:97422488
|
T | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(182): Show | 203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.-6-5972T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422488 | ||||||
chr9:97422503
|
T | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-5957T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422503 | ||||||
chr9:97422658
|
T | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-6-5802T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97422658 | ||||||
chr9:97422725
|
G | GT | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(63): Show | 75 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-6-5729dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97422725 | |||||
chr9:97423025
|
A | G | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-5435A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423025 | ||||||
chr9:97423211
|
G | A | 2 | a0001c0005t0001g0312a0001c0005t0001g0314 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-6-5249G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423211 | ||||||
chr9:97423398
|
C | CT | 18 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0283others(15): Show | 21 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-5050dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423398 | |||||
chr9:97423398
|
CT | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-5050delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423398 | |||||
chr9:97423566
|
A | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4894A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423566 | ||||||
chr9:97423581
|
T | TTC | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4875_-6-4874dup others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97423581 | |||||
chr9:97423701
|
A | C | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6-4759A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423701 | ||||||
chr9:97423789
|
T | C | 2 | a0002c0002t0001g0141a0002c0002t0001g0153 | 2 | HG00408.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-6-4671T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423789 | ||||||
chr9:97423804
|
G | T | 1 | a0002c0002t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-6-4656G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423804 | ||||||
chr9:97423857
|
A | G | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6-4603A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97423857 | ||||||
chr9:97424049
|
CT | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(126): Show | 148 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-6-4387delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97424049 | |||||
chr9:97424049
|
CTT | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 179 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.-6-4388_-6-4387del others(2): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 97424049 | |||||
chr9:97424086
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4374C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424086 | ||||||
chr9:97424148
|
A | G | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4312A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424148 | ||||||
chr9:97424200
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4260C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424200 | ||||||
chr9:97424308
|
G | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4152G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424308 | ||||||
chr9:97424362
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-4098C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424362 | ||||||
chr9:97424711
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6-3749A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424711 | ||||||
chr9:97424802
|
G | A | 1 | a0001c0004t0001g0318 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-6-3658G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424802 | ||||||
chr9:97424976
|
G | A | 3 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0317 | 3 | HG03209.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-3484G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97424976 | ||||||
chr9:97425006
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-3454G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425006 | ||||||
chr9:97425022
|
A | G | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-6-3438A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425022 | ||||||
chr9:97425156
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-3304G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425156 | ||||||
chr9:97425737
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-6-2723A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425737 | ||||||
chr9:97425824
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.-6-2636G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425824 | ||||||
chr9:97425847
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-6-2613T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425847 | ||||||
chr9:97425886
|
A | G | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6-2574A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97425886 | ||||||
chr9:97426707
|
T | A | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1753T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426707 | ||||||
chr9:97426709
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-6-1751C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426709 | ||||||
chr9:97426914
|
G | A | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-6-1546G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426914 | ||||||
chr9:97426930
|
C | G | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6-1530C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426930 | ||||||
chr9:97426941
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-6-1519C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97426941 | ||||||
chr9:97427071
|
A | G | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1389A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427071 | ||||||
chr9:97427255
|
T | C | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-1205T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427255 | ||||||
chr9:97427535
|
C | A | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-6-925C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427535 | ||||||
chr9:97427938
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-6-522T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427938 | ||||||
chr9:97427968
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0302 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-492A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97427968 | ||||||
chr9:97428049
|
T | C | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-6-411T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428049 | ||||||
chr9:97428214
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6-246C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428214 | ||||||
chr9:97428259
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-201G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428259 | ||||||
chr9:97428288
|
T | G | 1 | a0002c0002t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-6-172T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 1/16 | chr9 | 97428288 | ||||||
chr9:97428690
|
C | T | 22 | a0002c0002t0001g0051a0002c0002t0001g0183a0002c0002t0001g0206others(19): Show | 25 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.207+18C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428690 | ||||||
chr9:97428691
|
G | A | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.207+19G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428691 | ||||||
chr9:97428841
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.207+169T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428841 | ||||||
chr9:97428857
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.207+185C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428857 | ||||||
chr9:97428946
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207+274A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97428946 | ||||||
chr9:97429075
|
A | C | 1 | a0002c0002t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+403A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429075 | ||||||
chr9:97429167
|
G | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(72): Show | 85 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.207+495G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429167 | ||||||
chr9:97429418
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.207+746G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429418 | ||||||
chr9:97429451
|
G | C | 1 | a0002c0002t0002g0209 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.207+779G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429451 | ||||||
chr9:97429507
|
G | A | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.207+835G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429507 | ||||||
chr9:97429667
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.207+995G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429667 | ||||||
chr9:97429700
|
A | G | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.207+1028A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429700 | ||||||
chr9:97429713
|
A | G | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.207+1041A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429713 | ||||||
chr9:97429721
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+1049C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429721 | ||||||
chr9:97429903
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.208-1030T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429903 | ||||||
chr9:97429957
|
C | T | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0302 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.208-976C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97429957 | ||||||
chr9:97430035
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208-898A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430035 | ||||||
chr9:97430074
|
T | C | 2 | a0001c0004t0001g0315a0001c0004t0001g0316 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.208-859T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430074 | ||||||
chr9:97430264
|
G | A | 16 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-669G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430264 | ||||||
chr9:97430704
|
T | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 68 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-229T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430704 | ||||||
chr9:97430719
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.208-214A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430719 | ||||||
chr9:97430831
|
T | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.208-102T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 2/16 | chr9 | 97430831 | ||||||
chr9:97431529
|
A | G | 5 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0055others(2): Show | 5 | HG02132.hp1 NA18939.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+455A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431529 | ||||||
chr9:97431680
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.350-345C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431680 | ||||||
chr9:97431895
|
A | G | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-130A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97431895 | ||||||
chr9:97432015
|
A | G | 1 | a0001c0003t0001g0311 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.350-10A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 3/16 | chr9 | 97432015 | ||||||
chr9:97432252
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.563+14G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432252 | ||||||
chr9:97432355
|
G | C | 1 | a0001c0003t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.563+117G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432355 | ||||||
chr9:97432371
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0245a0001c0001t0001g0248others(5): Show | 9 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+133A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432371 | ||||||
chr9:97432388
|
G | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | NA18948.hp1 NA18999.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.563+150G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432388 | ||||||
chr9:97432543
|
G | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.563+305G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432543 | ||||||
chr9:97432714
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0106others(1): Show | 4 | HG01243.hp2 HG01255.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.563+476G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432714 | ||||||
chr9:97432717
|
A | G | 1 | a0002c0002t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.563+479A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432717 | ||||||
chr9:97432771
|
T | C | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.563+533T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97432771 | ||||||
chr9:97433159
|
G | T | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.563+921G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433159 | ||||||
chr9:97433502
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.563+1264G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433502 | ||||||
chr9:97433804
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.563+1566A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433804 | ||||||
chr9:97433816
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.563+1578T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433816 | ||||||
chr9:97433833
|
G | A | 27 | a0002c0002t0001g0020a0002c0002t0001g0028a0002c0002t0001g0052others(24): Show | 28 | HG00323.hp1 HG00544.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.563+1595G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433833 | ||||||
chr9:97433871
|
G | A | 1 | a0002c0008t0001g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.563+1633G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97433871 | ||||||
chr9:97434113
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.563+1875T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434113 | ||||||
chr9:97434379
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.563+2141C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434379 | ||||||
chr9:97434418
|
C | G | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+2180C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434418 | ||||||
chr9:97434733
|
A | G | 2 | a0002c0002t0001g0206a0002c0002t0001g0208 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.563+2495A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97434733 | ||||||
chr9:97435235
|
AT | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(177): Show | 197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.563+3001delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435235 | |||||
chr9:97435467
|
TA | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(139): Show | 158 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.563+3248delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435467 | |||||
chr9:97435496
|
C | T | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.563+3258C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435496 | ||||||
chr9:97435499
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(177): Show | 197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.563+3261G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435499 | ||||||
chr9:97435525
|
G | T | 17 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0033others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+3287G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435525 | ||||||
chr9:97435589
|
T | A | 1 | a0003c0006t0001g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.563+3351T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435589 | ||||||
chr9:97435628
|
C | CCTGT | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.563+3392_563+3393i others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 97435628 | |||||
chr9:97435910
|
C | G | 1 | a0002c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.564-3335C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435910 | ||||||
chr9:97435997
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.564-3248C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97435997 | ||||||
chr9:97436197
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564-3048A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436197 | ||||||
chr9:97436263
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.564-2982T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436263 | ||||||
chr9:97436399
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.564-2846T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436399 | ||||||
chr9:97436507
|
G | A | 2 | a0002c0002t0001g0119a0002c0002t0001g0154 | 2 | HG02155.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.564-2738G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436507 | ||||||
chr9:97436615
|
G | C | 5 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0317others(2): Show | 5 | HG02615.hp1 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.564-2630G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436615 | ||||||
chr9:97436867
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.564-2378T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97436867 | ||||||
chr9:97437052
|
C | A | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.564-2193C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437052 | ||||||
chr9:97437209
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.564-2036C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437209 | ||||||
chr9:97437217
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.564-2028T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437217 | ||||||
chr9:97437238
|
C | T | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.564-2007C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437238 | ||||||
chr9:97437291
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.564-1954A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437291 | ||||||
chr9:97437403
|
C | T | 1 | a0002c0002t0001g0310 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.564-1842C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437403 | ||||||
chr9:97437648
|
C | T | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.564-1597C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437648 | ||||||
chr9:97437726
|
G | A | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.564-1519G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437726 | ||||||
chr9:97437864
|
T | G | 17 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(14): Show | 18 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.564-1381T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437864 | ||||||
chr9:97437905
|
C | T | 1 | a0001c0003t0001g0311 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.564-1340C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437905 | ||||||
chr9:97437948
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.564-1297A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97437948 | ||||||
chr9:97438318
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.564-927A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438318 | ||||||
chr9:97438399
|
C | A | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.564-846C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438399 | ||||||
chr9:97438490
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.564-755C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438490 | ||||||
chr9:97438570
|
A | T | 8 | a0002c0002t0001g0174a0002c0002t0001g0175a0002c0002t0001g0176others(5): Show | 8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.564-675A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438570 | ||||||
chr9:97438693
|
A | G | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.564-552A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438693 | ||||||
chr9:97438868
|
T | C | 1 | a0001c0004t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564-377T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97438868 | ||||||
chr9:97439078
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(62): Show | 71 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.564-167A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439078 | ||||||
chr9:97439089
|
G | A | 1 | a0002c0002t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.564-156G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439089 | ||||||
chr9:97439127
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.564-118A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439127 | ||||||
chr9:97439177
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0001g0223 | 2 | HG00544.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.564-68G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 4/16 | chr9 | 97439177 | ||||||
chr9:97439382
|
G | A | 19 | a0002c0002t0001g0028a0002c0002t0001g0052a0002c0002t0001g0053others(16): Show | 19 | HG00323.hp1 HG00544.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.637+64G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439382 | ||||||
chr9:97439565
|
A | G | 4 | a0002c0002t0001g0186a0002c0002t0001g0216a0002c0002t0001g0235others(1): Show | 4 | HG02135.hp2 NA18943.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+247A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439565 | ||||||
chr9:97439592
|
C | T | 1 | a0002c0002t0002g0214 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.637+274C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439592 | ||||||
chr9:97439775
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.637+457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439775 | ||||||
chr9:97439803
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637+485G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439803 | ||||||
chr9:97439830
|
G | A | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.637+512G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439830 | ||||||
chr9:97439876
|
G | C | 1 | a0001c0003t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.637+558G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439876 | ||||||
chr9:97439951
|
C | T | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+633C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439951 | ||||||
chr9:97439960
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.637+642C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97439960 | ||||||
chr9:97440307
|
C | T | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+989C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440307 | ||||||
chr9:97440339
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.637+1021G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440339 | ||||||
chr9:97440381
|
G | C | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.637+1063G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440381 | ||||||
chr9:97440541
|
A | G | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0302 | 3 | HG02486.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.638-1117A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440541 | ||||||
chr9:97440602
|
C | T | 35 | a0001c0003t0001g0026a0001c0003t0001g0031a0001c0003t0001g0032others(32): Show | 36 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.638-1056C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440602 | ||||||
chr9:97440744
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.638-914A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440744 | ||||||
chr9:97440751
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.638-907A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440751 | ||||||
chr9:97440923
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.638-735C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440923 | ||||||
chr9:97440936
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.638-722A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440936 | ||||||
chr9:97440952
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.638-706G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97440952 | ||||||
chr9:97441426
|
G | T | 33 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0118others(30): Show | 33 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.638-232G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97441426 | ||||||
chr9:97441456
|
A | G | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638-202A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 5/16 | chr9 | 97441456 | ||||||
chr9:97441920
|
C | G | 7 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(4): Show | 9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.855+45C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97441920 | ||||||
chr9:97441950
|
T | C | 1 | a0002c0002t0001g0171 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+75T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97441950 | ||||||
chr9:97442176
|
TAAACACT others(10): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.855+302_855+318del others(17): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442176 | ||||||
chr9:97442194
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.855+319C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442194 | ||||||
chr9:97442436
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0294 | 2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.855+561T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442436 | ||||||
chr9:97442498
|
A | G | 1 | a0002c0002t0001g0055 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.855+623A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442498 | ||||||
chr9:97442576
|
G | T | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+701G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442576 | ||||||
chr9:97442604
|
C | T | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+729C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442604 | ||||||
chr9:97442827
|
CT | C | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+957delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97442827 | |||||
chr9:97442830
|
T | C | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+955T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442830 | ||||||
chr9:97442869
|
C | A | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.855+994C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97442869 | ||||||
chr9:97443119
|
C | T | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+1244C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443119 | ||||||
chr9:97443141
|
T | C | 37 | a0001c0001t0001g0324a0001c0003t0001g0026a0001c0003t0001g0031others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.855+1266T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443141 | ||||||
chr9:97443153
|
G | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.855+1278G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443153 | ||||||
chr9:97443260
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+1385T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443260 | ||||||
chr9:97443409
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.855+1534C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443409 | ||||||
chr9:97443410
|
A | G | 1 | a0002c0002t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.855+1535A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443410 | ||||||
chr9:97443561
|
A | G | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.855+1686A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443561 | ||||||
chr9:97443820
|
T | A | 1 | a0002c0002t0001g0138 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.855+1945T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443820 | ||||||
chr9:97443847
|
T | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(145): Show | 165 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.855+1972T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443847 | ||||||
chr9:97443925
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+2050C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97443925 | ||||||
chr9:97444222
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+2347C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444222 | ||||||
chr9:97444320
|
C | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 352 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.855+2445C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444320 | ||||||
chr9:97444344
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.855+2469A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444344 | ||||||
chr9:97444448
|
T | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+2573T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444448 | ||||||
chr9:97444821
|
C | T | 16 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+2946C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444821 | ||||||
chr9:97444904
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3029C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444904 | ||||||
chr9:97444972
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.855+3097G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97444972 | ||||||
chr9:97445093
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3218C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445093 | ||||||
chr9:97445285
|
TTTGAC | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(183): Show | 203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.855+3417_855+3421d others(7): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97445285 | |||||
chr9:97445316
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+3441C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445316 | ||||||
chr9:97445507
|
A | C | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.855+3632A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445507 | ||||||
chr9:97445537
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.855+3662G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445537 | ||||||
chr9:97445770
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.855+3895G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445770 | ||||||
chr9:97445888
|
G | T | 1 | a0001c0003t0001g0033 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.855+4013G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445888 | ||||||
chr9:97445984
|
T | G | 2 | a0002c0002t0001g0028a0002c0002t0001g0223 | 2 | HG00544.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.855+4109T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97445984 | ||||||
chr9:97446198
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.855+4323C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446198 | ||||||
chr9:97446536
|
G | A | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.855+4661G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446536 | ||||||
chr9:97446645
|
G | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.855+4770G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446645 | ||||||
chr9:97446915
|
A | G | 1 | a0002c0002t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.855+5040A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97446915 | ||||||
chr9:97447032
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+5157T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447032 | ||||||
chr9:97447242
|
G | A | 1 | a0002c0002t0001g0308 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.855+5367G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447242 | ||||||
chr9:97447276
|
G | A | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.855+5401G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447276 | ||||||
chr9:97447394
|
C | T | 1 | a0001c0003t0001g0031 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.855+5519C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447394 | ||||||
chr9:97447460
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.855+5585G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447460 | ||||||
chr9:97447720
|
GTAATGAG others(9): Show |
G | 1 | a0002c0002t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.855+5863_855+5878d others(18): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97447720 | |||||
chr9:97447887
|
C | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.855+6012C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97447887 | ||||||
chr9:97448543
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.855+6668T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448543 | ||||||
chr9:97448772
|
T | C | 8 | a0002c0002t0001g0183a0002c0002t0002g0012a0002c0002t0002g0168others(5): Show | 9 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.855+6897T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448772 | ||||||
chr9:97448840
|
G | C | 1 | a0002c0002t0002g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.855+6965G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97448840 | ||||||
chr9:97449258
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.855+7383G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449258 | ||||||
chr9:97449297
|
G | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+7422G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449297 | ||||||
chr9:97449412
|
C | T | 16 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.855+7537C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449412 | ||||||
chr9:97449424
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.855+7549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449424 | ||||||
chr9:97449432
|
C | T | 19 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(16): Show | 20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.855+7557C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449432 | ||||||
chr9:97449475
|
G | A | 2 | a0002c0002t0001g0235a0002c0002t0002g0322 | 2 | HG02135.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.855+7600G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449475 | ||||||
chr9:97449526
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.855+7651C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449526 | ||||||
chr9:97449587
|
T | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 303 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.855+7712T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449587 | ||||||
chr9:97449640
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0248 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.855+7765A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449640 | ||||||
chr9:97449656
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.855+7781G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449656 | ||||||
chr9:97449722
|
G | A | 1 | a0001c0004t0001g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.855+7847G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449722 | ||||||
chr9:97449726
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+7851T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449726 | ||||||
chr9:97449896
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.855+8021A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97449896 | ||||||
chr9:97450065
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.855+8190G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450065 | ||||||
chr9:97450121
|
C | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(279): Show | 303 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.855+8246C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450121 | ||||||
chr9:97450256
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.855+8381A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450256 | ||||||
chr9:97450627
|
T | TTAACTC | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+8752_855+8753i others(8): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450627 | ||||||
chr9:97450628
|
C | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+8753C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450628 | ||||||
chr9:97450901
|
G | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.855+9026G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450901 | ||||||
chr9:97450906
|
CT | C | 10 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG01515.hp2 HG01516.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.855+9046delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97450906 | |||||
chr9:97450908
|
T | C | 2 | a0001c0015t0001g0024a0002c0002t0001g0183 | 2 | HG02293.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.855+9033T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450908 | ||||||
chr9:97450990
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0325 | 3 | HG02015.hp1 NA18612.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.855+9115G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97450990 | ||||||
chr9:97451058
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.856-9120G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451058 | ||||||
chr9:97451089
|
A | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-9089A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451089 | ||||||
chr9:97451136
|
G | GC | 3 | a0001c0001t0001g0004a0001c0001t0001g0258a0001c0001t0001g0283 | 5 | NA18970.hp2 NA18971.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-9041dupC | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97451136 | |||||
chr9:97451230
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-8948C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451230 | ||||||
chr9:97451283
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.856-8895T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451283 | ||||||
chr9:97451355
|
T | C | 1 | a0001c0003t0001g0311 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.856-8823T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451355 | ||||||
chr9:97451439
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-8739A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451439 | ||||||
chr9:97451446
|
C | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8732C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451446 | ||||||
chr9:97451530
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8648T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451530 | ||||||
chr9:97451536
|
C | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0294 | 2 | HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.856-8642C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451536 | ||||||
chr9:97451563
|
A | T | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-8615A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451563 | ||||||
chr9:97451819
|
G | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8359G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451819 | ||||||
chr9:97451860
|
TTGAC | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8314_856-8311d others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97451860 | |||||
chr9:97451880
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.856-8298C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451880 | ||||||
chr9:97451887
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-8291C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451887 | ||||||
chr9:97451920
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-8258T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451920 | ||||||
chr9:97451921
|
T | G | 1 | a0001c0004t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.856-8257T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97451921 | ||||||
chr9:97452104
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-8074C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452104 | ||||||
chr9:97452189
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-7989G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452189 | ||||||
chr9:97452196
|
G | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-7982G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452196 | ||||||
chr9:97452458
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.856-7720A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452458 | ||||||
chr9:97452565
|
G | A | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.856-7613G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452565 | ||||||
chr9:97452626
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-7552T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452626 | ||||||
chr9:97452678
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.856-7500G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452678 | ||||||
chr9:97452800
|
C | T | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0292others(1): Show | 4 | NA18941.hp1 NA18974.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-7378C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97452800 | ||||||
chr9:97453025
|
C | T | 2 | a0001c0001t0001g0094a0008c0012t0001g0076 | 2 | NA19011.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.856-7153C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453025 | ||||||
chr9:97453139
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(141): Show | 159 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.856-7039G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453139 | ||||||
chr9:97453145
|
G | A | 1 | a0007c0014t0001g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.856-7033G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453145 | ||||||
chr9:97453154
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856-7024A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453154 | ||||||
chr9:97453173
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.856-7005C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453173 | ||||||
chr9:97453425
|
T | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(319): Show | 352 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.856-6753T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453425 | ||||||
chr9:97453459
|
T | G | 5 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0139others(2): Show | 5 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-6719T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453459 | ||||||
chr9:97453529
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-6649T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453529 | ||||||
chr9:97453676
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-6502T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453676 | ||||||
chr9:97453677
|
C | T | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-6501C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453677 | ||||||
chr9:97453874
|
A | G | 2 | a0002c0002t0001g0119a0002c0002t0001g0154 | 2 | HG02155.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.856-6304A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97453874 | ||||||
chr9:97454076
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.856-6102A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454076 | ||||||
chr9:97454128
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.856-6050T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454128 | ||||||
chr9:97454134
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 202 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.856-6044G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454134 | ||||||
chr9:97454282
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-5896C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454282 | ||||||
chr9:97454285
|
C | A | 2 | a0002c0002t0001g0020a0002c0002t0004g0110 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.856-5893C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454285 | ||||||
chr9:97454429
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.856-5749C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454429 | ||||||
chr9:97454436
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.856-5742G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454436 | ||||||
chr9:97454480
|
C | T | 1 | a0001c0004t0001g0318 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856-5698C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454480 | ||||||
chr9:97454486
|
AAGAG | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-5688_856-5685d others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr9 | 97454486 | |||||
chr9:97454501
|
G | A | 1 | a0002c0002t0001g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.856-5677G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454501 | ||||||
chr9:97454749
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.856-5429G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97454749 | ||||||
chr9:97455024
|
A | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-5154A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455024 | ||||||
chr9:97455087
|
A | T | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-5091A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455087 | ||||||
chr9:97455209
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-4969G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455209 | ||||||
chr9:97455519
|
C | T | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.856-4659C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455519 | ||||||
chr9:97455653
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-4525T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455653 | ||||||
chr9:97455994
|
A | G | 2 | a0001c0001t0001g0027a0001c0009t0001g0323 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.856-4184A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97455994 | ||||||
chr9:97456076
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(183): Show | 202 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.856-4102C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456076 | ||||||
chr9:97456246
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3932T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456246 | ||||||
chr9:97456357
|
T | A | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(255): Show | 279 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(276): Show |
intron_variant | MODIFIER | c.856-3821T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456357 | ||||||
chr9:97456441
|
G | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3737G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456441 | ||||||
chr9:97456485
|
G | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-3693G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456485 | ||||||
chr9:97456705
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856-3473C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456705 | ||||||
chr9:97456709
|
C | T | 9 | a0002c0002t0001g0183a0002c0002t0001g0213a0002c0002t0002g0012others(6): Show | 10 | HG01167.hp2 HG01934.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-3469C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456709 | ||||||
chr9:97456864
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.856-3314C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456864 | ||||||
chr9:97456909
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-3269A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97456909 | ||||||
chr9:97457008
|
G | A | 1 | a0002c0002t0001g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.856-3170G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457008 | ||||||
chr9:97457195
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.856-2983A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457195 | ||||||
chr9:97457198
|
A | G | 1 | a0001c0003t0001g0040 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.856-2980A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457198 | ||||||
chr9:97457292
|
C | T | 1 | a0002c0002t0001g0306 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856-2886C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457292 | ||||||
chr9:97457387
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.856-2791T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457387 | ||||||
chr9:97457388
|
T | A | 5 | a0001c0009t0001g0323a0002c0002t0001g0194a0002c0002t0001g0195others(2): Show | 5 | HG01081.hp2 HG01358.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-2790T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457388 | ||||||
chr9:97457452
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.856-2726C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457452 | ||||||
chr9:97457455
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856-2723T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457455 | ||||||
chr9:97457464
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-2714T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457464 | ||||||
chr9:97457680
|
A | G | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.856-2498A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457680 | ||||||
chr9:97457776
|
G | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 70 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.856-2402G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457776 | ||||||
chr9:97457820
|
T | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.856-2358T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457820 | ||||||
chr9:97457928
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(74): Show | 87 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.856-2250A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457928 | ||||||
chr9:97457958
|
A | T | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-2220A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457958 | ||||||
chr9:97457976
|
C | A | 1 | a0002c0002t0001g0213 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.856-2202C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97457976 | ||||||
chr9:97458013
|
A | G | 1 | a0002c0002t0001g0306 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.856-2165A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458013 | ||||||
chr9:97458061
|
G | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-2117G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458061 | ||||||
chr9:97458219
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0289 | 2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.856-1959G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458219 | ||||||
chr9:97458242
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.856-1936G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458242 | ||||||
chr9:97458306
|
T | A | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-1872T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458306 | ||||||
chr9:97458341
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.856-1837G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458341 | ||||||
chr9:97458387
|
T | C | 1 | a0001c0004t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.856-1791T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458387 | ||||||
chr9:97458524
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(254): Show | 278 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.856-1654G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458524 | ||||||
chr9:97458539
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.856-1639C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458539 | ||||||
chr9:97458849
|
G | A | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 197 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.856-1329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458849 | ||||||
chr9:97458877
|
T | C | 2 | a0001c0001t0001g0324a0001c0003t0001g0033 | 2 | HG02074.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.856-1301T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458877 | ||||||
chr9:97458921
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.856-1257C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97458921 | ||||||
chr9:97459508
|
T | G | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-670T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459508 | ||||||
chr9:97459680
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.856-498C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459680 | ||||||
chr9:97459686
|
A | G | 1 | a0002c0002t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.856-492A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459686 | ||||||
chr9:97459751
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-427G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459751 | ||||||
chr9:97459752
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-426G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459752 | ||||||
chr9:97459891
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856-287G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97459891 | ||||||
chr9:97460036
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.856-142G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97460036 | ||||||
chr9:97460061
|
C | A | 1 | a0002c0002t0001g0175 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.856-117C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 6/16 | chr9 | 97460061 | ||||||
chr9:97460815
|
G | T | 1 | a0001c0001t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1442+51G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97460815 | ||||||
chr9:97460868
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1442+104G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97460868 | ||||||
chr9:97461033
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+269C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461033 | ||||||
chr9:97461048
|
A | G | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1442+284A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461048 | ||||||
chr9:97461140
|
C | CAA | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+389_1442+390d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97461140 | |||||
chr9:97461157
|
A | G | 1 | a0002c0002t0001g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1442+393A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461157 | ||||||
chr9:97461188
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+424T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461188 | ||||||
chr9:97461197
|
A | G | 3 | a0001c0001t0001g0291a0001c0001t0001g0321a0002c0002t0001g0170 | 3 | HG00438.hp2 HG00544.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1442+433A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461197 | ||||||
chr9:97461238
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+474A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461238 | ||||||
chr9:97461296
|
A | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+532A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461296 | ||||||
chr9:97461351
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1442+587G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461351 | ||||||
chr9:97461363
|
A | C | 19 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(16): Show | 20 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1442+599A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461363 | ||||||
chr9:97461479
|
CCAAAGGT others(17): Show |
C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1442+717_1442+740d others(26): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97461479 | |||||
chr9:97461535
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+771A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461535 | ||||||
chr9:97461639
|
C | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+875C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461639 | ||||||
chr9:97461930
|
T | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1166T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97461930 | ||||||
chr9:97462086
|
C | T | 10 | a0002c0002t0001g0141a0002c0002t0001g0143a0002c0002t0001g0147others(7): Show | 10 | HG00408.hp2 HG02015.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1442+1322C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462086 | ||||||
chr9:97462126
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1442+1362T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462126 | ||||||
chr9:97462243
|
C | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1479C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462243 | ||||||
chr9:97462313
|
G | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1442+1549G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462313 | ||||||
chr9:97462475
|
A | G | 1 | a0002c0002t0001g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1442+1711A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462475 | ||||||
chr9:97462505
|
CT | C | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1442+1742delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462505 | ||||||
chr9:97462646
|
T | G | 1 | a0001c0003t0001g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1442+1882T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462646 | ||||||
chr9:97462701
|
A | G | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442+1937A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462701 | ||||||
chr9:97462758
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1442+1994A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462758 | ||||||
chr9:97462963
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-1879C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97462963 | ||||||
chr9:97463019
|
A | T | 1 | a0002c0002t0001g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1443-1823A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463019 | ||||||
chr9:97463023
|
G | T | 1 | a0001c0004t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1443-1819G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463023 | ||||||
chr9:97463244
|
C | CA | 20 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(17): Show | 21 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1443-1588dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463244 | |||||
chr9:97463375
|
G | GT | 13 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(10): Show | 13 | HG00408.hp1 HG02074.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1443-1463dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463375 | |||||
chr9:97463375
|
G | GTT | 5 | a0001c0003t0001g0037a0001c0003t0001g0038a0001c0003t0001g0039others(2): Show | 5 | HG00558.hp1 NA18984.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443-1464_1443-146 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463375 | |||||
chr9:97463380
|
G | GT | 10 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG01175.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1443-1445dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463380 | |||||
chr9:97463380
|
G | T | 20 | a0001c0001t0001g0173a0001c0001t0001g0324a0001c0003t0001g0031others(17): Show | 20 | HG00408.hp1 HG00558.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1443-1462G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463380 | ||||||
chr9:97463380
|
GT | G | 7 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0093others(4): Show | 7 | HG01952.hp1 HG02630.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1443-1445delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97463380 | |||||
chr9:97463608
|
C | A | 4 | a0002c0002t0001g0159a0002c0002t0001g0160a0002c0002t0001g0161others(1): Show | 4 | NA18953.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443-1234C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463608 | ||||||
chr9:97463664
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-1178C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463664 | ||||||
chr9:97463734
|
G | A | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1443-1108G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463734 | ||||||
chr9:97463810
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1443-1032G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463810 | ||||||
chr9:97463975
|
T | C | 1 | a0002c0002t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1443-867T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97463975 | ||||||
chr9:97464154
|
G | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-688G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464154 | ||||||
chr9:97464349
|
G | A | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1443-493G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464349 | ||||||
chr9:97464653
|
G | A | 1 | a0002c0002t0001g0136 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1443-189G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464653 | ||||||
chr9:97464700
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.1443-142G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464700 | ||||||
chr9:97464729
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.1443-113T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464729 | ||||||
chr9:97464735
|
T | C | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1443-107T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | chr9 | 97464735 | ||||||
chr9:97464761
|
AAAG | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1443-77_1443-75del others(3): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 97464761 | |||||
chr9:97465035
|
A | G | 6 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0094others(3): Show | 6 | HG04115.hp2 NA18960.hp2 NA18969.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1629+7A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465035 | ||||||
chr9:97465078
|
A | G | 1 | a0002c0002t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1629+50A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465078 | ||||||
chr9:97465141
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1629+113G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465141 | ||||||
chr9:97465309
|
A | G | 1 | a0002c0002t0001g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1629+281A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465309 | ||||||
chr9:97465370
|
G | A | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1629+342G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465370 | ||||||
chr9:97465694
|
G | T | 1 | a0002c0002t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1629+666G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97465694 | ||||||
chr9:97466112
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1629+1084A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466112 | ||||||
chr9:97466333
|
T | C | 1 | a0002c0002t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1629+1305T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466333 | ||||||
chr9:97466451
|
TA | T | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 199 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.1629+1425delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 97466451 | |||||
chr9:97466621
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1629+1593A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466621 | ||||||
chr9:97466874
|
A | T | 3 | a0002c0002t0001g0116a0002c0002t0001g0117a0002c0002t0001g0118 | 3 | HG01261.hp1 HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1629+1846A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466874 | ||||||
chr9:97466990
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(72): Show | 85 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1629+1962A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97466990 | ||||||
chr9:97467108
|
A | G | 8 | a0002c0002t0001g0174a0002c0002t0001g0175a0002c0002t0001g0176others(5): Show | 8 | HG01081.hp1 HG01243.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629+2080A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467108 | ||||||
chr9:97467115
|
T | C | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1629+2087T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467115 | ||||||
chr9:97467124
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1629+2096G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467124 | ||||||
chr9:97467273
|
A | G | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1629+2245A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467273 | ||||||
chr9:97467293
|
C | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(181): Show | 201 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.1629+2265C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467293 | ||||||
chr9:97467355
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1629+2327C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467355 | ||||||
chr9:97467486
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1629+2458C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97467486 | ||||||
chr9:97468120
|
A | G | 1 | a0002c0002t0002g0212 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1630-2438A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468120 | ||||||
chr9:97468124
|
G | T | 1 | a0002c0002t0001g0174 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1630-2434G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468124 | ||||||
chr9:97468219
|
C | T | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1630-2339C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468219 | ||||||
chr9:97468264
|
G | A | 26 | a0001c0003t0001g0042a0001c0003t0001g0043a0002c0002t0001g0020others(23): Show | 30 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1630-2294G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468264 | ||||||
chr9:97468391
|
C | T | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1630-2167C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468391 | ||||||
chr9:97468412
|
T | C | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1630-2146T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468412 | ||||||
chr9:97468496
|
G | A | 2 | a0001c0001t0001g0027a0001c0009t0001g0323 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1630-2062G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468496 | ||||||
chr9:97468512
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1630-2046C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468512 | ||||||
chr9:97468558
|
G | A | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1630-2000G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468558 | ||||||
chr9:97468690
|
C | T | 2 | a0002c0002t0001g0186a0002c0002t0001g0216 | 2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1630-1868C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468690 | ||||||
chr9:97468691
|
G | A | 3 | a0001c0001t0001g0291a0001c0001t0001g0321a0002c0002t0001g0170 | 3 | HG00438.hp2 HG00544.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1630-1867G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468691 | ||||||
chr9:97468854
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1630-1704G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97468854 | ||||||
chr9:97469136
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1630-1422C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469136 | ||||||
chr9:97469318
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG00558.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1630-1240A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469318 | ||||||
chr9:97469459
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1630-1099T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469459 | ||||||
chr9:97469862
|
T | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.1630-696T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97469862 | ||||||
chr9:97470035
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1630-523G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470035 | ||||||
chr9:97470107
|
C | A | 1 | a0002c0002t0001g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1630-451C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470107 | ||||||
chr9:97470175
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1630-383A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470175 | ||||||
chr9:97470315
|
C | T | 1 | a0001c0003t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1630-243C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470315 | ||||||
chr9:97470359
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1630-199T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 8/16 | chr9 | 97470359 | ||||||
chr9:97470864
|
T | C | 4 | a0002c0002t0001g0178a0002c0002t0001g0179a0002c0002t0001g0180others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+195T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470864 | ||||||
chr9:97470874
|
C | T | 2 | a0002c0002t0001g0155a0002c0002t0001g0157 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1741+205C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470874 | ||||||
chr9:97470907
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 163 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1741+238C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97470907 | ||||||
chr9:97471040
|
T | G | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1741+371T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471040 | ||||||
chr9:97471058
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1741+389A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471058 | ||||||
chr9:97471080
|
A | G | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741+411A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471080 | ||||||
chr9:97471113
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1741+444A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471113 | ||||||
chr9:97471241
|
C | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 204 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.1741+572C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471241 | ||||||
chr9:97471336
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1741+667T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471336 | ||||||
chr9:97471355
|
C | T | 2 | a0003c0006t0001g0005a0003c0006t0001g0030 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1741+686C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471355 | ||||||
chr9:97471363
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741+694G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471363 | ||||||
chr9:97471570
|
A | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1742-723A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97471570 | ||||||
chr9:97472064
|
G | T | 1 | a0002c0002t0001g0135 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1742-229G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472064 | ||||||
chr9:97472119
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.1742-174T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472119 | ||||||
chr9:97472263
|
G | A | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1742-30G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472263 | ||||||
chr9:97472265
|
A | C | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1742-28A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 9/16 | chr9 | 97472265 | ||||||
chr9:97472753
|
A | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(139): Show | 157 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1944+258A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97472753 | ||||||
chr9:97473435
|
A | G | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1945-57A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97473435 | ||||||
chr9:97473445
|
T | G | 2 | a0002c0002t0001g0225a0002c0002t0001g0226 | 2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1945-47T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 10/16 | chr9 | 97473445 | ||||||
chr9:97473835
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0247a0001c0001t0001g0257others(9): Show | 14 | NA18941.hp1 NA18954.hp1 NA18967.hp2 others(11): Show |
intron_variant | MODIFIER | c.2079+209G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473835 | ||||||
chr9:97473866
|
C | T | 1 | a0001c0005t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2079+240C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473866 | ||||||
chr9:97473871
|
G | C | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2079+245G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97473871 | ||||||
chr9:97474181
|
T | A | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+555T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474181 | ||||||
chr9:97474193
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0325 | 3 | HG02015.hp1 NA18612.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.2079+567T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474193 | ||||||
chr9:97474453
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2079+827C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474453 | ||||||
chr9:97474464
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+838C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474464 | ||||||
chr9:97474471
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2079+845T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474471 | ||||||
chr9:97474523
|
G | A | 16 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2080-860G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474523 | ||||||
chr9:97474551
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2080-832G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474551 | ||||||
chr9:97474756
|
A | C | 1 | a0002c0002t0001g0226 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2080-627A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474756 | ||||||
chr9:97474905
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2080-478A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97474905 | ||||||
chr9:97475023
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0095 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2080-360A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475023 | ||||||
chr9:97475066
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0254a0001c0001t0001g0287 | 4 | NA18747.hp2 NA18942.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2080-317A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475066 | ||||||
chr9:97475115
|
A | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2080-268A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475115 | ||||||
chr9:97475237
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2080-146C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475237 | ||||||
chr9:97475244
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG02145.hp1 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2080-139T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 11/16 | chr9 | 97475244 | ||||||
chr9:97475491
|
T | G | 1 | a0001c0001t0001g0284 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2166+22T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475491 | ||||||
chr9:97475535
|
G | GT | 16 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(13): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2166+73dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97475535 | |||||
chr9:97475757
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2166+288T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475757 | ||||||
chr9:97475762
|
T | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2166+293T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475762 | ||||||
chr9:97475858
|
G | A | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(182): Show | 203 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.2166+389G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97475858 | ||||||
chr9:97476028
|
C | G | 1 | a0002c0002t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2166+559C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476028 | ||||||
chr9:97476028
|
C | T | 2 | a0002c0002t0001g0020a0002c0002t0004g0110 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2166+559C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476028 | ||||||
chr9:97476236
|
C | A | 2 | a0002c0002t0001g0020a0002c0002t0004g0110 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2166+767C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476236 | ||||||
chr9:97476271
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2166+802G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476271 | ||||||
chr9:97476369
|
G | A | 1 | a0001c0004t0001g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2166+900G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476369 | ||||||
chr9:97476394
|
A | G | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2166+925A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476394 | ||||||
chr9:97476564
|
G | GA | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(162): Show | 183 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.2166+1109dupA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97476564 | |||||
chr9:97476564
|
G | GAA | 20 | a0001c0001t0001g0075a0001c0001t0001g0096a0001c0001t0001g0324others(17): Show | 20 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.2166+1108_2166+110 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 97476564 | |||||
chr9:97476595
|
T | G | 1 | a0002c0002t0001g0196 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2166+1126T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476595 | ||||||
chr9:97476806
|
C | T | 4 | a0001c0005t0001g0105a0001c0005t0001g0312a0001c0005t0001g0313others(1): Show | 4 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2166+1337C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476806 | ||||||
chr9:97476852
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2166+1383A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476852 | ||||||
chr9:97476934
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2166+1465T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97476934 | ||||||
chr9:97477213
|
A | G | 7 | a0001c0003t0001g0032a0001c0003t0001g0035a0001c0003t0001g0036others(4): Show | 7 | HG00408.hp1 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.2167-1226A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477213 | ||||||
chr9:97477368
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 178 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.2167-1071C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477368 | ||||||
chr9:97477885
|
C | G | 1 | a0001c0001t0001g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2167-554C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477885 | ||||||
chr9:97477923
|
A | G | 1 | a0001c0003t0001g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2167-516A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477923 | ||||||
chr9:97477987
|
G | A | 1 | a0001c0009t0001g0323 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167-452G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477987 | ||||||
chr9:97477989
|
T | C | 1 | a0002c0002t0001g0188 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2167-450T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97477989 | ||||||
chr9:97478004
|
A | T | 1 | a0002c0002t0002g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2167-435A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478004 | ||||||
chr9:97478125
|
G | C | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2167-314G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478125 | ||||||
chr9:97478158
|
G | A | 1 | a0002c0002t0001g0170 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167-281G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478158 | ||||||
chr9:97478309
|
G | A | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2167-130G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 12/16 | chr9 | 97478309 | ||||||
chr9:97478733
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2301+160T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97478733 | ||||||
chr9:97478997
|
A | G | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2301+424A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97478997 | ||||||
chr9:97480183
|
C | A | 1 | a0002c0002t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2302-645C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480183 | ||||||
chr9:97480427
|
A | ATT | 17 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(14): Show | 17 | HG00558.hp1 HG02074.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.2302-387_2302-386d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 97480427 | |||||
chr9:97480481
|
C | A | 1 | a0002c0002t0001g0170 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2302-347C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480481 | ||||||
chr9:97480518
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2302-310C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 13/16 | chr9 | 97480518 | ||||||
chr9:97481026
|
C | T | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+88C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481026 | ||||||
chr9:97481137
|
T | C | 1 | a0002c0002t0001g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2412+199T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481137 | ||||||
chr9:97481405
|
A | G | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2412+467A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481405 | ||||||
chr9:97481413
|
T | A | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+475T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481413 | ||||||
chr9:97481503
|
GT | G | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2412+570delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr9 | 97481503 | |||||
chr9:97481567
|
C | T | 10 | a0002c0002t0001g0141a0002c0002t0001g0143a0002c0002t0001g0147others(7): Show | 10 | HG00408.hp2 HG02015.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2412+629C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481567 | ||||||
chr9:97481889
|
G | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 305 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.2412+951G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481889 | ||||||
chr9:97481958
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2413-891C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97481958 | ||||||
chr9:97482106
|
G | A | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2413-743G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482106 | ||||||
chr9:97482176
|
A | G | 1 | a0002c0002t0001g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2413-673A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482176 | ||||||
chr9:97482235
|
G | A | 1 | a0001c0003t0001g0037 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2413-614G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482235 | ||||||
chr9:97482253
|
C | T | 1 | a0002c0002t0001g0189 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2413-596C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482253 | ||||||
chr9:97482519
|
C | T | 21 | a0001c0001t0001g0182a0001c0003t0001g0026a0001c0004t0001g0010others(18): Show | 22 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2413-330C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482519 | ||||||
chr9:97482520
|
G | A | 4 | a0002c0002t0001g0119a0002c0002t0001g0138a0002c0002t0001g0145others(1): Show | 4 | HG02155.hp2 NA18954.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482520 | ||||||
chr9:97482547
|
A | G | 1 | a0002c0002t0002g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2413-302A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482547 | ||||||
chr9:97482550
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2413-299A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482550 | ||||||
chr9:97482732
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2413-117G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 14/16 | chr9 | 97482732 | ||||||
chr9:97483371
|
A | T | 1 | a0002c0002t0001g0206 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2915+20A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483371 | ||||||
chr9:97483402
|
A | G | 1 | a0002c0002t0001g0206 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2915+51A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483402 | ||||||
chr9:97483438
|
C | T | 1 | a0001c0003t0001g0031 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2915+87C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483438 | ||||||
chr9:97483558
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0258a0001c0001t0001g0283 | 5 | NA18970.hp2 NA18971.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915+207A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97483558 | ||||||
chr9:97484469
|
A | AAC | 4 | a0001c0001t0001g0297a0001c0001t0001g0298a0002c0002t0001g0127others(1): Show | 4 | HG02683.hp2 HG04204.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+1141_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484469 | |||||
chr9:97484469
|
AAC | A | 18 | a0001c0003t0001g0026a0001c0004t0001g0010a0001c0004t0001g0102others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2915+1141_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484469 | |||||
chr9:97484485
|
C | G | 1 | a0002c0002t0001g0176 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2915+1134C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484485 | ||||||
chr9:97484488
|
A | C | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2915+1137A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484488 | ||||||
chr9:97484490
|
A | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 69 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.2915+1139A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484490 | ||||||
chr9:97484492
|
A | ACC | 9 | a0001c0001t0001g0106a0001c0001t0001g0166a0001c0001t0001g0167others(6): Show | 9 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2915+1144_2915+114 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr9 | 97484492 | |||||
chr9:97484492
|
A | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 170 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.2915+1141A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484492 | ||||||
chr9:97484604
|
A | G | 1 | a0002c0002t0001g0188 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2915+1253A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484604 | ||||||
chr9:97484652
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2915+1301C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484652 | ||||||
chr9:97484722
|
A | G | 1 | a0002c0002t0001g0162 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2915+1371A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484722 | ||||||
chr9:97484850
|
G | C | 1 | a0001c0003t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2915+1499G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97484850 | ||||||
chr9:97485000
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2915+1649C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485000 | ||||||
chr9:97485038
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2915+1687T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485038 | ||||||
chr9:97485045
|
A | T | 1 | a0002c0002t0001g0213 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2915+1694A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485045 | ||||||
chr9:97485442
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2916-1730C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485442 | ||||||
chr9:97485583
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-1589C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485583 | ||||||
chr9:97485715
|
A | G | 4 | a0002c0002t0001g0119a0002c0002t0001g0138a0002c0002t0001g0145others(1): Show | 4 | HG02155.hp2 NA18954.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-1457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485715 | ||||||
chr9:97485760
|
A | G | 1 | a0002c0002t0002g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2916-1412A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485760 | ||||||
chr9:97485875
|
C | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2916-1297C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485875 | ||||||
chr9:97485960
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-1212G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97485960 | ||||||
chr9:97486037
|
G | A | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916-1135G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486037 | ||||||
chr9:97486196
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2916-976A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486196 | ||||||
chr9:97486242
|
T | C | 1 | a0002c0002t0001g0197 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2916-930T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486242 | ||||||
chr9:97486637
|
A | G | 17 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2916-535A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486637 | ||||||
chr9:97486647
|
C | G | 2 | a0002c0002t0001g0121a0002c0002t0001g0217 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2916-525C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486647 | ||||||
chr9:97486879
|
A | C | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2916-293A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486879 | ||||||
chr9:97486879
|
A | G | 1 | a0002c0002t0001g0149 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2916-293A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97486879 | ||||||
chr9:97487048
|
G | A | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2916-124G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 15/16 | chr9 | 97487048 | ||||||
chr9:97487442
|
G | A | 1 | a0002c0002t0001g0051 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3076+110G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487442 | ||||||
chr9:97487471
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3076+139C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487471 | ||||||
chr9:97487548
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3076+216C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487548 | ||||||
chr9:97487641
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 198 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.3076+309G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487641 | ||||||
chr9:97487678
|
G | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3076+346G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487678 | ||||||
chr9:97487679
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3076+347T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487679 | ||||||
chr9:97487681
|
C | CTACTTGT others(1): Show |
16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.3076+351_3076+358d others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97487681 | |||||
chr9:97487694
|
A | T | 1 | a0001c0003t0001g0039 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3076+362A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487694 | ||||||
chr9:97487877
|
A | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 182 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.3076+545A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97487877 | ||||||
chr9:97488329
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3076+997A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488329 | ||||||
chr9:97488465
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3076+1133A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488465 | ||||||
chr9:97488560
|
G | GT | 123 | a0001c0001t0001g0092a0001c0001t0001g0241a0001c0001t0001g0324others(120): Show | 136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3076+1247dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | |||||
chr9:97488560
|
G | GTT | 21 | a0001c0003t0001g0038a0001c0003t0001g0045a0002c0002t0001g0117others(18): Show | 21 | HG00621.hp2 HG01109.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.3076+1246_3076+124 others(6): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | |||||
chr9:97488560
|
GT | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(145): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.3076+1247delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97488560 | |||||
chr9:97488568
|
T | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 161 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.3076+1236T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488568 | ||||||
chr9:97488572
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.3076+1240T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488572 | ||||||
chr9:97488574
|
T | G | 1 | a0001c0004t0001g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3076+1242T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488574 | ||||||
chr9:97488575
|
T | G | 3 | a0001c0005t0001g0313a0003c0006t0001g0005a0003c0006t0001g0030 | 4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+1243T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488575 | ||||||
chr9:97488576
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 162 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.3076+1244T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488576 | ||||||
chr9:97488580
|
G | T | 5 | a0001c0009t0001g0323a0002c0002t0001g0125a0002c0002t0001g0147others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3076+1248G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488580 | ||||||
chr9:97488602
|
G | A | 3 | a0001c0005t0001g0313a0003c0006t0001g0005a0003c0006t0001g0030 | 4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+1270G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488602 | ||||||
chr9:97488640
|
T | C | 1 | a0001c0001t0001g0006 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3076+1308T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488640 | ||||||
chr9:97488744
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0115a0001c0001t0001g0263others(3): Show | 8 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.3076+1412G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488744 | ||||||
chr9:97488833
|
C | T | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3076+1501C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97488833 | ||||||
chr9:97489068
|
C | T | 1 | a0002c0002t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3076+1736C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489068 | ||||||
chr9:97489081
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.3076+1749G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489081 | ||||||
chr9:97489130
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3076+1798G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489130 | ||||||
chr9:97489173
|
G | A | 3 | a0002c0002t0001g0194a0002c0002t0001g0195a0002c0002t0001g0199 | 3 | HG00323.hp2 HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3076+1841G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489173 | ||||||
chr9:97489293
|
A | G | 1 | a0002c0002t0001g0130 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3076+1961A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489293 | ||||||
chr9:97489506
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3076+2174C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489506 | ||||||
chr9:97489754
|
G | T | 3 | a0002c0002t0001g0230a0002c0002t0001g0231a0002c0002t0002g0307 | 3 | HG02818.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3076+2422G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489754 | ||||||
chr9:97489786
|
C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3076+2454C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489786 | ||||||
chr9:97489986
|
CA | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0001g0059others(11): Show | 14 | HG01070.hp1 HG01261.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.3076+2655delA | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97489986 | ||||||
chr9:97490011
|
G | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(186): Show | 207 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.3076+2679G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490011 | ||||||
chr9:97490031
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3076+2699C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490031 | ||||||
chr9:97490034
|
G | GCACACA | 16 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(13): Show | 16 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.3076+2712_3076+271 others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490034 | |||||
chr9:97490061
|
C | G | 1 | a0002c0002t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3076+2729C>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490061 | ||||||
chr9:97490068
|
A | G | 1 | a0001c0004t0001g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3076+2736A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490068 | ||||||
chr9:97490158
|
C | A | 3 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0056 | 3 | NA19055.hp1 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3076+2826C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490158 | ||||||
chr9:97490439
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(165): Show | 185 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.3076+3107T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490439 | ||||||
chr9:97490471
|
G | T | 18 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(15): Show | 18 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3076+3139G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490471 | ||||||
chr9:97490549
|
T | TG | 76 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0057others(73): Show | 79 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.3076+3228dupG | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490549 | |||||
chr9:97490553
|
G | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0094a0001c0001t0001g0096others(2): Show | 5 | NA18960.hp2 NA18969.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.3076+3221G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490553 | ||||||
chr9:97490557
|
G | C | 1 | a0001c0003t0001g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3076+3225G>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490557 | ||||||
chr9:97490559
|
G | A | 1 | a0002c0002t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3076+3227G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490559 | ||||||
chr9:97490572
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3076+3240C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490572 | ||||||
chr9:97490576
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3076+3244G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490576 | ||||||
chr9:97490610
|
G | T | 2 | a0002c0002t0003g0205a0002c0002t0003g0232 | 2 | NA19078.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3076+3278G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490610 | ||||||
chr9:97490634
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3076+3302C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490634 | ||||||
chr9:97490872
|
G | T | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG01256.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.3076+3540G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97490872 | ||||||
chr9:97490904
|
CTTTTCT | C | 15 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(12): Show | 15 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.3076+3577_3076+358 others(10): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490904 | |||||
chr9:97490909
|
C | CT | 54 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0079others(51): Show | 57 | HG00438.hp1 HG00621.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.3076+3601dupT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490909 | |||||
chr9:97490909
|
CT | C | 6 | a0001c0001t0001g0256a0001c0001t0001g0279a0001c0001t0001g0300others(3): Show | 6 | HG00323.hp2 HG01123.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.3076+3601delT | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97490909 | |||||
chr9:97491139
|
A | G | 25 | a0001c0001t0001g0261a0001c0001t0001g0324a0001c0003t0001g0032others(22): Show | 25 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.3076+3807A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491139 | ||||||
chr9:97491372
|
C | A | 1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3076+4040C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491372 | ||||||
chr9:97491376
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3076+4044A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491376 | ||||||
chr9:97491445
|
T | C | 3 | a0001c0005t0001g0313a0003c0006t0001g0005a0003c0006t0001g0030 | 4 | HG02976.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3076+4113T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491445 | ||||||
chr9:97491537
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(142): Show | 160 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.3077-4126A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491537 | ||||||
chr9:97491539
|
G | A | 1 | a0001c0005t0001g0313 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3077-4124G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491539 | ||||||
chr9:97491570
|
T | C | 4 | a0002c0002t0001g0051a0002c0002t0003g0002a0002c0002t0003g0204others(1): Show | 6 | NA18941.hp2 NA18962.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.3077-4093T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491570 | ||||||
chr9:97491741
|
G | A | 1 | a0002c0002t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3077-3922G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491741 | ||||||
chr9:97491914
|
A | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3077-3749A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97491914 | ||||||
chr9:97492206
|
A | G | 2 | a0002c0002t0001g0189a0002c0002t0001g0193 | 2 | HG01981.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.3077-3457A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492206 | ||||||
chr9:97492403
|
T | C | 19 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(16): Show | 19 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-3260T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492403 | ||||||
chr9:97492568
|
A | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0059 | 2 | HG01975.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3077-3095A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492568 | ||||||
chr9:97492808
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3077-2855C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97492808 | ||||||
chr9:97493093
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3077-2570T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493093 | ||||||
chr9:97493140
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0245a0001c0001t0001g0248others(6): Show | 10 | HG02572.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3077-2523C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493140 | ||||||
chr9:97493164
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 161 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.3077-2499G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493164 | ||||||
chr9:97493248
|
T | C | 1 | a0001c0003t0001g0039 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3077-2415T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493248 | ||||||
chr9:97493272
|
C | T | 4 | a0001c0001t0001g0182a0001c0005t0001g0313a0003c0006t0001g0005others(1): Show | 5 | HG02976.hp1 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3077-2391C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493272 | ||||||
chr9:97493277
|
G | A | 3 | a0002c0002t0001g0053a0002c0002t0001g0056a0002c0002t0001g0207 | 3 | HG01433.hp1 NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3077-2386G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493277 | ||||||
chr9:97493321
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01255.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3077-2342A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493321 | ||||||
chr9:97493334
|
G | A | 18 | a0001c0001t0001g0027a0001c0003t0001g0026a0001c0004t0001g0010others(15): Show | 19 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-2329G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493334 | ||||||
chr9:97493393
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3077-2270G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493393 | ||||||
chr9:97493424
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3077-2239A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493424 | ||||||
chr9:97493426
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3077-2237T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493426 | ||||||
chr9:97493571
|
C | T | 15 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3077-2092C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493571 | ||||||
chr9:97493681
|
G | A | 1 | a0002c0002t0001g0188 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3077-1982G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493681 | ||||||
chr9:97493814
|
C | T | 1 | a0002c0002t0001g0055 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3077-1849C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493814 | ||||||
chr9:97493867
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3077-1796C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493867 | ||||||
chr9:97493904
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3077-1759T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493904 | ||||||
chr9:97493916
|
A | G | 1 | a0002c0002t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3077-1747A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493916 | ||||||
chr9:97493944
|
G | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0289 | 2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.3077-1719G>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97493944 | ||||||
chr9:97494000
|
A | G | 19 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(16): Show | 19 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3077-1663A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494000 | ||||||
chr9:97494002
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3077-1661C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494002 | ||||||
chr9:97494091
|
A | G | 14 | a0001c0003t0001g0031a0001c0003t0001g0032a0001c0003t0001g0035others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.3077-1572A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494091 | ||||||
chr9:97494147
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18969.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3077-1516A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494147 | ||||||
chr9:97494178
|
A | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 301 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.3077-1485A>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494178 | ||||||
chr9:97494178
|
A | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0093a0001c0001t0001g0095 | 3 | HG02109.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3077-1485A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494178 | ||||||
chr9:97494327
|
T | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0084 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3077-1336T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494327 | ||||||
chr9:97494360
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3077-1303G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494360 | ||||||
chr9:97494392
|
C | T | 4 | a0002c0002t0001g0191a0002c0002t0002g0012a0002c0002t0002g0209others(1): Show | 5 | HG01167.hp2 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.3077-1271C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494392 | ||||||
chr9:97494694
|
GTA | G | 12 | a0001c0003t0001g0026a0001c0004t0001g0112a0001c0004t0001g0315others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3077-951_3077-950d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494694 | |||||
chr9:97494698
|
A | ATATATAT others(7): Show |
4 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(1): Show | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.3077-952_3077-951i others(16): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494698 | |||||
chr9:97494709
|
TATA | T | 6 | a0001c0005t0001g0313a0001c0009t0001g0323a0002c0002t0001g0126others(3): Show | 7 | HG02630.hp2 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3077-953_3077-951d others(5): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494709 | ||||||
chr9:97494710
|
A | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0072others(5): Show | 8 | HG00438.hp2 HG00544.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-953A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494710 | ||||||
chr9:97494712
|
A | T | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(171): Show | 188 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.3077-951A>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494712 | ||||||
chr9:97494712
|
ATTTTT | A | 14 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3077-942_3077-938d others(7): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494712 | |||||
chr9:97494714
|
T | A | 9 | a0001c0004t0001g0010a0001c0004t0001g0102a0001c0004t0001g0103others(6): Show | 10 | HG00639.hp1 HG00673.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.3077-949T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494714 | ||||||
chr9:97494722
|
T | C | 7 | a0001c0001t0001g0047a0001c0005t0001g0313a0001c0009t0001g0323others(4): Show | 8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-941T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494722 | ||||||
chr9:97494723
|
T | G | 7 | a0001c0001t0001g0047a0001c0005t0001g0313a0001c0009t0001g0323others(4): Show | 8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-940T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494723 | ||||||
chr9:97494724
|
T | A | 7 | a0001c0001t0001g0047a0001c0005t0001g0313a0001c0009t0001g0323others(4): Show | 8 | HG01109.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3077-939T>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | ||||||
chr9:97494724
|
T | C | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 220 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(217): Show |
intron_variant | MODIFIER | c.3077-939T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | ||||||
chr9:97494724
|
T | TC | 14 | a0001c0001t0001g0018a0001c0001t0001g0078a0001c0001t0001g0241others(11): Show | 15 | HG00639.hp2 HG02683.hp2 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.3077-939_3077-938i others(3): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494724 | ||||||
chr9:97494725
|
T | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 243 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.3077-938T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494725 | ||||||
chr9:97494726
|
C | A | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 243 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.3077-937C>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494726 | ||||||
chr9:97494726
|
C | CGA | 9 | a0001c0001t0001g0027a0001c0001t0001g0245a0001c0001t0001g0248others(6): Show | 10 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3077-933_3077-932d others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494726 | |||||
chr9:97494729
|
G | GAC | 17 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-933_3077-932i others(4): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 97494729 | |||||
chr9:97494738
|
A | ATTTTGTC others(3): Show |
1 | a0006c0011t0001g0025 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3077-925_3077-924i others(12): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494738 | ||||||
chr9:97494781
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3077-882G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494781 | ||||||
chr9:97494814
|
G | A | 1 | a0001c0015t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3077-849G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494814 | ||||||
chr9:97494871
|
C | T | 17 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-792C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494871 | ||||||
chr9:97494923
|
C | T | 1 | a0002c0002t0001g0224 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3077-740C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494923 | ||||||
chr9:97494930
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3077-733C>T | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494930 | ||||||
chr9:97494931
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3077-732G>A | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97494931 | ||||||
chr9:97495068
|
T | G | 1 | a0002c0002t0001g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3077-595T>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495068 | ||||||
chr9:97495130
|
T | C | 23 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(20): Show | 24 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.3077-533T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495130 | ||||||
chr9:97495139
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(185): Show | 206 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.3077-524A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495139 | ||||||
chr9:97495332
|
T | C | 17 | a0001c0001t0001g0324a0001c0003t0001g0031a0001c0003t0001g0032others(14): Show | 17 | HG00408.hp1 HG00558.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.3077-331T>C | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495332 | ||||||
chr9:97495336
|
TATTTTAT others(17): Show |
T | 1 | a0001c0001t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3077-326_3077-303d others(26): Show |
TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495336 | ||||||
chr9:97495375
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3077-288A>G | TDRD7 | ENSG00000196116.8 | transcript | ENST00000355295.5 | protein_coding | 16/16 | chr9 | 97495375 |