geneid | 55357 |
---|---|
ensemblid | ENSG00000095383.20 |
hgncid | 18026 |
symbol | TBC1D2 |
name | TBC1 domain family member 2 |
refseq_nuc | NM_001267571.2 |
refseq_prot | NP_001254500.1 |
ensembl_nuc | ENST00000465784.7 |
ensembl_prot | ENSP00000481721.1 |
mane_status | MANE Select |
chr | chr9 |
start | 98199011 |
end | 98255649 |
strand | - |
ver | v1.2 |
region | chr9:98199011-98255649 |
region5000 | chr9:98194011-98260649 |
regionname0 | TBC1D2_chr9_98199011_98255649 |
regionname5000 | TBC1D2_chr9_98194011_98260649 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 928 | 197 | 16 | 42 | 105 | 9 | 23 | 87 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002 | 0/0 | 928 | 74 | 10 | 15 | 38 | 3 | 8 | 32 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003 | 0/0 | 928 | 55 | 40 | 9 | 3 | 2 | 1 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0004 | 0/0 | 928 | 8 | 3 | 2 | 0 | 2 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0005 | 0/0 | 928 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006 | 0/0 | 928 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0007 | 0/0 | 928 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0008 | 0/0 | 928 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0009 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0010 | 0/0 | 25 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0011 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0012 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0013 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0014 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0015 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0016 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0017 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0018 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0019 | 0/0 | 928 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0020 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0021 | 0/0 | 928 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0022 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0023 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0024 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2787 | 99 | 9 | 17 | 56 | 3 | 13 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0002 | 1/0 | 2787 | 82 | 2 | 19 | 44 | 6 | 10 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0003 | 0/0 | 2787 | 65 | 3 | 13 | 38 | 3 | 8 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0004 | 0/0 | 2787 | 42 | 29 | 7 | 3 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0005 | 0/0 | 2787 | 8 | 3 | 2 | 0 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0006 | 0/0 | 2787 | 7 | 1 | 4 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0007 | 0/0 | 2787 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0008 | 0/0 | 2787 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0009 | 0/0 | 2787 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0010 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0011 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0012 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0013 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0014 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0015 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0016 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0017 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0018 | 0/0 | 2787 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0019 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0020 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0021 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0022 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0023 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0024 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0025 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0026 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0027 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0028 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0029 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0030 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0031 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0032 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0033 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0034 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0035 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0036 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0037 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0038 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0039 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0040 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
c0041 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 479 | 364 | 87 | 70 | 153 | 16 | 36 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
t0002 | 0/0 | 479 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
t0003 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0012 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2787 | 99 | 9 | 17 | 56 | 3 | 13 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0002 | 1/0 | 2787 | 82 | 2 | 19 | 44 | 6 | 10 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0006 | 0/0 | 2787 | 7 | 1 | 4 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0008 | 0/0 | 2787 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0019 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0039 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0003 | 0/0 | 2787 | 65 | 3 | 13 | 38 | 3 | 8 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0007 | 0/0 | 2787 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0014 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0030 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0004 | 0/0 | 2787 | 42 | 29 | 7 | 3 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0009 | 0/0 | 2787 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0011 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0012 | 0/0 | 2787 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0026 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0034 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0036 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0004c0005 | 0/0 | 2787 | 8 | 3 | 2 | 0 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0005c0010 | 0/0 | 2787 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0005c0015 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0016 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0035 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0038 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0007c0017 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0008c0018 | 0/0 | 2787 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0009c0013 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0010c0020 | 0/0 | 2787 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0011c0024 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0012c0040 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0013c0041 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0014c0025 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0015c0037 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0016c0021 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0017c0027 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0018c0029 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0019c0031 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0020c0032 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0021c0028 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0022c0033 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0023c0023 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0024c0022 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3265 | 99 | 9 | 17 | 56 | 3 | 13 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0002t0001 | 1/0 | 3265 | 81 | 2 | 19 | 43 | 6 | 10 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0002t0002 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0006t0001 | 0/0 | 3265 | 7 | 1 | 4 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0008t0001 | 0/0 | 3265 | 6 | 4 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0019t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0001c0039t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0003t0001 | 0/0 | 3265 | 65 | 3 | 13 | 38 | 3 | 8 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0007t0001 | 0/0 | 3265 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0014t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0002c0030t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0004t0001 | 0/0 | 3265 | 41 | 28 | 7 | 3 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0004t0003 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0009t0001 | 0/0 | 3265 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0011t0001 | 0/0 | 3265 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0012t0001 | 0/0 | 3265 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0026t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0034t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0003c0036t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0004c0005t0001 | 0/0 | 3265 | 8 | 3 | 2 | 0 | 2 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0005c0010t0001 | 0/0 | 3265 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0005c0015t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0016t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0035t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0006c0038t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0007c0017t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0008c0018t0001 | 0/0 | 3265 | 2 | 0 | 1 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0009c0013t0001 | 0/0 | 3265 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0010c0020t0001 | 0/0 | 3265 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0011c0024t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0012c0040t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0013c0041t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0014c0025t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0015c0037t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0016c0021t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0017c0027t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0018c0029t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0019c0031t0001 | 0/0 | 3265 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0020c0032t0001 | 0/0 | 3265 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0021c0028t0001 | 0/0 | 3265 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0022c0033t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0023c0023t0001 | 0/0 | 3265 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
a0024c0022t0001 | 0/0 | 3265 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | copy fasta | chr9 | 98194011 | 98260649 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0012 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0006t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0006t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0006t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0006t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0008t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0019t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0019t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0001c0039t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0007t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0007t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0014t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0002c0030t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0004t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0009t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0009t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0009t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0011t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0011t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0011t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0012t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0012t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0012t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0026t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0034t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0003c0036t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0004c0005t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0010t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0010t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0015t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0005c0015t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0006c0016t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0006c0016t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0006c0035t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0006c0038t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0007c0017t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0007c0017t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0008c0018t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0008c0018t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0009c0013t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0009c0013t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0010c0020t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0010c0020t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0011c0024t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0012c0040t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0013c0041t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0014c0025t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0015c0037t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0016c0021t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0017c0027t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0018c0029t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0019c0031t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0020c0032t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0021c0028t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0022c0033t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0023c0023t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
a0024c0022t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0001 | g0280 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0175 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0165 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00140 | hp2 | a0004 | c0005 | t0001 | g0079 | EUR | GBR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00280 | hp1 | a0003 | c0004 | t0001 | g0313 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0142 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00323 | hp1 | a0003 | c0004 | t0001 | g0310 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00323 | hp2 | a0002 | c0003 | t0001 | g0248 | EUR | FIN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00408 | hp1 | a0003 | c0004 | t0001 | g0298 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00438 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00544 | hp1 | a0001 | c0039 | t0001 | g0059 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00597 | hp2 | a0012 | c0040 | t0001 | g0147 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0225 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0251 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0307 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00733 | hp1 | a0004 | c0005 | t0001 | g0279 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0250 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00738 | hp1 | a0004 | c0005 | t0001 | g0278 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0255 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0254 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01071 | hp2 | a0008 | c0018 | t0001 | g0075 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01081 | hp1 | a0003 | c0004 | t0001 | g0045 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01081 | hp2 | a0001 | c0008 | t0001 | g0123 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01099 | hp1 | a0002 | c0003 | t0001 | g0218 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01106 | hp1 | a0020 | c0032 | t0001 | g0234 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0300 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01168 | hp1 | a0003 | c0004 | t0001 | g0301 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01169 | hp2 | a0003 | c0004 | t0001 | g0302 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01243 | hp1 | a0003 | c0004 | t0001 | g0299 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01243 | hp2 | a0003 | c0026 | t0001 | g0041 | AMR | PUR | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01255 | hp1 | a0001 | c0008 | t0001 | g0122 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01255 | hp2 | a0003 | c0009 | t0001 | g0033 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0019 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01258 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01346 | hp1 | a0001 | c0006 | t0001 | g0143 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0020 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0219 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01361 | hp2 | a0002 | c0030 | t0001 | g0252 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0263 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01496 | hp2 | a0002 | c0007 | t0001 | g0239 | AMR | CLM | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0324 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0145 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0247 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0146 | EUR | IBS | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0327 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01884 | hp2 | a0005 | c0015 | t0001 | g0031 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01891 | hp1 | a0003 | c0004 | t0001 | g0102 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01891 | hp2 | a0003 | c0004 | t0003 | g0046 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0258 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01952 | hp2 | a0003 | c0004 | t0001 | g0311 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01975 | hp1 | a0002 | c0003 | t0001 | g0242 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01993 | hp1 | a0001 | c0006 | t0001 | g0013 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02015 | hp1 | a0002 | c0003 | t0001 | g0232 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0270 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02129 | hp1 | a0010 | c0020 | t0001 | g0336 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02129 | hp2 | a0003 | c0004 | t0001 | g0309 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02145 | hp1 | a0009 | c0013 | t0001 | g0024 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CDX | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0244 | EAS | CDX | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0289 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02258 | hp2 | a0002 | c0014 | t0001 | g0026 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02273 | hp2 | a0001 | c0006 | t0001 | g0161 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0314 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02280 | hp2 | a0023 | c0023 | t0001 | g0028 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02293 | hp2 | a0001 | c0006 | t0001 | g0171 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0020 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02451 | hp1 | a0003 | c0009 | t0001 | g0032 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02451 | hp2 | a0003 | c0004 | t0001 | g0293 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02572 | hp1 | a0003 | c0004 | t0001 | g0283 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02572 | hp2 | a0009 | c0013 | t0001 | g0023 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0246 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02615 | hp1 | a0003 | c0011 | t0001 | g0044 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02615 | hp2 | a0003 | c0004 | t0001 | g0296 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02622 | hp1 | a0004 | c0005 | t0001 | g0281 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02622 | hp2 | a0001 | c0008 | t0001 | g0124 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0273 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02630 | hp2 | a0005 | c0010 | t0001 | g0038 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02698 | hp1 | a0008 | c0018 | t0001 | g0076 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02698 | hp2 | a0019 | c0031 | t0001 | g0257 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02717 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02717 | hp2 | a0003 | c0012 | t0001 | g0284 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02723 | hp1 | a0002 | c0007 | t0001 | g0002 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02723 | hp2 | a0003 | c0004 | t0001 | g0057 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02735 | hp1 | a0021 | c0028 | t0001 | g0243 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0217 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0268 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02738 | hp2 | a0003 | c0004 | t0001 | g0316 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02809 | hp1 | a0002 | c0007 | t0001 | g0002 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02809 | hp2 | a0003 | c0004 | t0001 | g0323 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02818 | hp1 | a0005 | c0010 | t0001 | g0037 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02818 | hp2 | a0014 | c0025 | t0001 | g0039 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02895 | hp1 | a0006 | c0016 | t0001 | g0049 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02895 | hp2 | a0002 | c0007 | t0001 | g0002 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0292 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02897 | hp2 | a0002 | c0007 | t0001 | g0002 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02922 | hp1 | a0003 | c0004 | t0001 | g0321 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0282 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02970 | hp1 | a0005 | c0015 | t0001 | g0030 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0320 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02976 | hp1 | a0006 | c0038 | t0001 | g0294 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0318 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0322 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03041 | hp2 | a0011 | c0024 | t0001 | g0080 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03098 | hp1 | a0003 | c0004 | t0001 | g0287 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03098 | hp2 | a0018 | c0029 | t0001 | g0274 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03130 | hp2 | a0003 | c0004 | t0001 | g0305 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0312 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03195 | hp1 | a0016 | c0021 | t0001 | g0022 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03195 | hp2 | a0003 | c0036 | t0001 | g0288 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03209 | hp1 | a0003 | c0011 | t0001 | g0029 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03209 | hp2 | a0003 | c0004 | t0001 | g0315 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0306 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03453 | hp1 | a0003 | c0012 | t0001 | g0291 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0304 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0303 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03486 | hp2 | a0001 | c0008 | t0001 | g0126 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03490 | hp1 | a0002 | c0003 | t0001 | g0267 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0245 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03516 | hp1 | a0003 | c0009 | t0001 | g0036 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03516 | hp2 | a0015 | c0037 | t0001 | g0043 | AFR | ESN | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03540 | hp1 | a0003 | c0004 | t0001 | g0308 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03579 | hp1 | a0003 | c0011 | t0001 | g0042 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03579 | hp2 | a0017 | c0027 | t0001 | g0275 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0249 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0227 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03710 | hp2 | a0004 | c0005 | t0001 | g0276 | SAS | PJL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04199 | hp1 | a0002 | c0003 | t0001 | g0264 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18522 | hp1 | a0003 | c0012 | t0001 | g0290 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18522 | hp2 | a0004 | c0005 | t0001 | g0277 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | CHB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18612 | hp2 | a0002 | c0003 | t0001 | g0238 | EAS | CHB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0286 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0228 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18945 | hp2 | a0001 | c0006 | t0001 | g0014 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18947 | hp1 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0233 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18952 | hp1 | a0001 | c0019 | t0001 | g0173 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0261 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0224 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18975 | hp1 | a0007 | c0017 | t0001 | g0162 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18977 | hp1 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18978 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0260 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18981 | hp1 | a0007 | c0017 | t0001 | g0157 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18981 | hp2 | a0013 | c0041 | t0001 | g0109 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18994 | hp1 | a0002 | c0003 | t0001 | g0269 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0231 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19003 | hp2 | a0022 | c0033 | t0001 | g0253 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19005 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19010 | hp1 | a0001 | c0019 | t0001 | g0172 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19030 | hp1 | a0005 | c0010 | t0001 | g0034 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19030 | hp2 | a0001 | c0008 | t0001 | g0127 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19043 | hp1 | a0002 | c0007 | t0001 | g0272 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19058 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19060 | hp1 | a0024 | c0022 | t0001 | g0027 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19062 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19063 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19064 | hp2 | a0001 | c0006 | t0001 | g0014 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19068 | hp1 | a0003 | c0004 | t0001 | g0297 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19077 | hp1 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19077 | hp2 | a0010 | c0020 | t0001 | g0335 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA19240 | hp2 | a0003 | c0009 | t0001 | g0040 | AFR | YRI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0125 | AFR | ASW | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20129 | hp2 | a0003 | c0004 | t0001 | g0285 | AFR | ASW | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0229 | EUR | TSI | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02109 | hp1 | a0002 | c0014 | t0001 | g0025 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02109 | hp2 | a0006 | c0035 | t0001 | g0295 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02559 | hp1 | a0004 | c0005 | t0001 | g0078 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG02559 | hp2 | a0005 | c0010 | t0001 | g0035 | AFR | ACB | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03471 | hp1 | a0003 | c0004 | t0001 | g0317 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
HG03471 | hp2 | a0006 | c0016 | t0001 | g0048 | AFR | MSL | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | USA | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA20300 | hp2 | a0003 | c0004 | t0001 | g0319 | AFR | USA | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA21309 | hp1 | a0003 | c0034 | t0001 | g0047 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0210 | REF | REF | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0012 | REF | REF | TBC1D2_chr9_98194011_98260649 | TBC1D2 | chr9 | 98194011 | 98260649 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:98199407
|
C | T | 1 | a0012 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.2761G>A | p.Glu921Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2869/3265 | 2761/2787 | 921/928 | chr9 | 98199407 | ||
chr9:98199487
|
C | T | 3 | a0006a0009a0016 | 7 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.2681G>A | p.Arg894Gln | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2789/3265 | 2681/2787 | 894/928 | chr9 | 98199487 | ||
chr9:98208732
|
G | A | 1 | a0019 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2086C>T | p.Arg696Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2194/3265 | 2086/2787 | 696/928 | chr9 | 98208732 | ||
chr9:98208815
|
C | T | 1 | a0018 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2003G>A | p.Arg668His | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2111/3265 | 2003/2787 | 668/928 | chr9 | 98208815 | ||
chr9:98208816
|
G | A | 1 | a0015 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2002C>T | p.Arg668Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2110/3265 | 2002/2787 | 668/928 | chr9 | 98208816 | ||
chr9:98208846
|
G | A | 1 | a0020 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1972C>T | p.Arg658Trp | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2080/3265 | 1972/2787 | 658/928 | chr9 | 98208846 | ||
chr9:98209032
|
C | T | 1 | a0021 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1786G>A | p.Glu596Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1894/3265 | 1786/2787 | 596/928 | chr9 | 98209032 | ||
chr9:98209050
|
G | T | 1 | a0013 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1768C>A | p.His590Asn | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1876/3265 | 1768/2787 | 590/928 | chr9 | 98209050 | ||
chr9:98210833
|
A | C | 1 | a0008 | 2 | HG01071.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.1496T>G | p.Leu499Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/13 | 1604/3265 | 1496/2787 | 499/928 | chr9 | 98210833 | ||
chr9:98213130
|
T | C | 1 | a0022 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1463A>G | p.Lys488Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/13 | 1571/3265 | 1463/2787 | 488/928 | chr9 | 98213130 | ||
chr9:98213199
|
C | T | 1 | a0007 | 2 | NA18975.hp1 NA18981.hp1 |
missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/13 | 1502/3265 | 1394/2787 | 465/928 | chr9 | 98213199 | ||
chr9:98220933
|
A | G | 3 | a0014a0016a0017 | 3 | HG02818.hp2 HG03195.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.1274T>C | p.Val425Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1382/3265 | 1274/2787 | 425/928 | chr9 | 98220933 | ||
chr9:98221047
|
G | A | 2 | a0005a0023 | 7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.1160C>T | p.Ala387Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1268/3265 | 1160/2787 | 387/928 | chr9 | 98221047 | ||
chr9:98229148
|
C | A | 10 | a0002a0009a0016others(7): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
missense_variant&splice_region_variant | MODERATE | c.782G>T | p.Gly261Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/13 | 890/3265 | 782/2787 | 261/928 | chr9 | 98229148 | ||
chr9:98233439
|
A | G | 16 | a0002a0003a0004others(13): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
missense_variant | MODERATE | c.758T>C | p.Leu253Ser | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 866/3265 | 758/2787 | 253/928 | chr9 | 98233439 | ||
chr9:98233476
|
G | T | 11 | a0002a0004a0009others(8): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
missense_variant | MODERATE | c.721C>A | p.Pro241Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 829/3265 | 721/2787 | 241/928 | chr9 | 98233476 | ||
chr9:98244129
|
C | T | 1 | a0011 | 1 | HG03041.hp2 | missense_variant&splice_region_variant | MODERATE | c.512G>A | p.Gly171Glu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/13 | 620/3265 | 512/2787 | 171/928 | chr9 | 98244129 | ||
chr9:98255274
|
A | C | 1 | a0023 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.268T>G | p.Leu90Val | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 376/3265 | 268/2787 | 90/928 | chr9 | 98255274 | ||
chr9:98255283
|
C | T | 1 | a0024 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.259G>A | p.Ala87Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 367/3265 | 259/2787 | 87/928 | chr9 | 98255283 | ||
chr9:98255541
|
T | C | 1 | a0010 | 2 | HG02129.hp1 NA19077.hp2 |
start_lost | HIGH | c.1A>G | p.Met1? | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 109/3265 | 1/2787 | 1/928 | chr9 | 98255541 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:98199408
|
G | A | 1 | a0002c0030 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.2760C>T | p.Ser920Ser | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 2868/3265 | 2760/2787 | 920/928 | chr9 | 98199408 | ||
chr9:98200330
|
C | T | 3 | a0003c0036a0006c0035a0006c0038 | 3 | HG02109.hp2 HG02976.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.2502G>A | p.Lys834Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/13 | 2610/3265 | 2502/2787 | 834/928 | chr9 | 98200330 | ||
chr9:98201593
|
G | A | 1 | a0001c0019 | 2 | NA18952.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.2343C>T | p.His781His | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/13 | 2451/3265 | 2343/2787 | 781/928 | chr9 | 98201593 | ||
chr9:98208832
|
G | A | 1 | a0001c0006 | 7 | HG01346.hp1 HG01993.hp1 HG02273.hp2 others(4): Show |
synonymous_variant | LOW | c.1986C>T | p.Arg662Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 2094/3265 | 1986/2787 | 662/928 | chr9 | 98208832 | ||
chr9:98209066
|
T | C | 30 | a0001c0001a0001c0039a0002c0003others(27): Show | 251 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
synonymous_variant | LOW | c.1752A>G | p.Ala584Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/13 | 1860/3265 | 1752/2787 | 584/928 | chr9 | 98209066 | ||
chr9:98210754
|
G | C | 2 | a0001c0008a0003c0012 | 9 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.1575C>G | p.Ala525Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/13 | 1683/3265 | 1575/2787 | 525/928 | chr9 | 98210754 | ||
chr9:98220947
|
C | T | 2 | a0003c0036a0006c0035 | 2 | HG02109.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1260G>A | p.Lys420Lys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1368/3265 | 1260/2787 | 420/928 | chr9 | 98220947 | ||
chr9:98221118
|
C | T | 1 | a0001c0039 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.1089G>A | p.Arg363Arg | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1197/3265 | 1089/2787 | 363/928 | chr9 | 98221118 | ||
chr9:98221201
|
G | A | 1 | a0003c0026 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1006C>T | p.Leu336Leu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/13 | 1114/3265 | 1006/2787 | 336/928 | chr9 | 98221201 | ||
chr9:98233438
|
C | T | 1 | a0003c0034 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.759G>A | p.Leu253Leu | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/13 | 867/3265 | 759/2787 | 253/928 | chr9 | 98233438 | ||
chr9:98244056
|
A | T | 6 | a0003c0009a0003c0026a0005c0010others(3): Show | 14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
synonymous_variant | LOW | c.585T>A | p.Ala195Ala | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/13 | 693/3265 | 585/2787 | 195/928 | chr9 | 98244056 | ||
chr9:98251834
|
G | T | 1 | a0005c0015 | 2 | HG01884.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.462C>A | p.Thr154Thr | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/13 | 570/3265 | 462/2787 | 154/928 | chr9 | 98251834 | ||
chr9:98255395
|
A | G | 3 | a0002c0014a0009c0013a0016c0021 | 5 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
synonymous_variant | LOW | c.147T>C | p.Cys49Cys | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 255/3265 | 147/2787 | 49/928 | chr9 | 98255395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:98199371
|
G | T | 1 | a0003c0004t0003 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 13/13 | 10 | chr9 | 98199371 | |||||
chr9:98255552
|
C | T | 1 | a0001c0002t0002 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/13 | 11 | chr9 | 98255552 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:98199646
|
C | T | 31 | a0001c0001t0001g0163a0001c0001t0001g0164a0002c0003t0001g0282others(28): Show | 33 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2580-58G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199646 | ||||||
chr9:98199670
|
G | A | 15 | a0003c0004t0001g0057a0003c0004t0001g0283a0003c0004t0001g0287others(12): Show | 15 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2580-82C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199670 | ||||||
chr9:98199727
|
A | G | 6 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0221others(3): Show | 8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.2580-139T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199727 | ||||||
chr9:98199845
|
C | A | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2580-257G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199845 | ||||||
chr9:98199959
|
A | G | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2579+294T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98199959 | ||||||
chr9:98200222
|
G | C | 10 | a0001c0001t0001g0008a0002c0003t0001g0217a0002c0003t0001g0229others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2579+31C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 12/12 | chr9 | 98200222 | ||||||
chr9:98200380
|
G | A | 1 | a0001c0002t0001g0094 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.2458-6C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200380 | ||||||
chr9:98200462
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2458-88T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200462 | ||||||
chr9:98200485
|
G | A | 8 | a0003c0004t0001g0283a0003c0004t0001g0289a0003c0004t0001g0292others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2458-111C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200485 | ||||||
chr9:98200520
|
A | G | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2458-146T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200520 | ||||||
chr9:98200564
|
T | TG | 12 | a0001c0001t0001g0053a0001c0001t0001g0112a0001c0001t0001g0118others(9): Show | 12 | HG00642.hp1 HG01192.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.2458-191dupC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200564 | ||||||
chr9:98200572
|
C | T | 56 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(53): Show | 61 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.2458-198G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200572 | ||||||
chr9:98200721
|
A | G | 58 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(55): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2458-347T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200721 | ||||||
chr9:98200742
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(165): Show | 181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.2458-368T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200742 | ||||||
chr9:98200744
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2458-370T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200744 | ||||||
chr9:98200807
|
G | T | 12 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(9): Show | 12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2458-433C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98200807 | ||||||
chr9:98201015
|
C | CA | 10 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0090others(7): Show | 10 | HG00438.hp2 HG00639.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2457+463dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | ||||||
chr9:98201015
|
C | CAA | 13 | a0002c0003t0001g0327a0003c0004t0001g0057a0003c0004t0001g0283others(10): Show | 13 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2457+462_2457+463d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | ||||||
chr9:98201015
|
CA | C | 14 | a0001c0001t0001g0100a0001c0001t0001g0197a0001c0001t0001g0208others(11): Show | 14 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2457+463delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201015 | ||||||
chr9:98201180
|
C | T | 58 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(55): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.2457+299G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201180 | ||||||
chr9:98201371
|
T | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(165): Show | 181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.2457+108A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 11/12 | chr9 | 98201371 | ||||||
chr9:98201677
|
G | A | 8 | a0003c0036t0001g0288a0006c0016t0001g0048a0006c0016t0001g0049others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2272-13C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201677 | ||||||
chr9:98201695
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0118a0001c0001t0001g0325others(1): Show | 4 | HG00642.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-31G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201695 | ||||||
chr9:98201841
|
A | G | 1 | a0016c0021t0001g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2272-177T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201841 | ||||||
chr9:98201858
|
C | T | 1 | a0018c0029t0001g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2272-194G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201858 | ||||||
chr9:98201932
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0193a0001c0001t0001g0196others(8): Show | 12 | HG01099.hp2 HG01192.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.2272-268G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98201932 | ||||||
chr9:98202039
|
T | C | 12 | a0003c0004t0001g0057a0003c0004t0001g0283a0003c0004t0001g0287others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2272-375A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202039 | ||||||
chr9:98202082
|
A | C | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(167): Show | 183 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-418T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202082 | ||||||
chr9:98202170
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2272-506C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202170 | ||||||
chr9:98202186
|
C | T | 1 | a0001c0006t0001g0161 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2272-522G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202186 | ||||||
chr9:98202188
|
C | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(62): Show | 71 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2272-524G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202188 | ||||||
chr9:98202369
|
C | T | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2272-705G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202369 | ||||||
chr9:98202419
|
T | C | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.2272-755A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202419 | ||||||
chr9:98202440
|
G | A | 1 | a0001c0002t0001g0176 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2272-776C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202440 | ||||||
chr9:98202467
|
C | T | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(170): Show | 186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2272-803G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202467 | ||||||
chr9:98202631
|
G | A | 1 | a0018c0029t0001g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2271+657C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202631 | ||||||
chr9:98202662
|
C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(164): Show | 180 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2271+626G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202662 | ||||||
chr9:98202702
|
G | T | 2 | a0001c0002t0001g0184a0001c0002t0001g0186 | 2 | HG00741.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2271+586C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202702 | ||||||
chr9:98202726
|
C | T | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2271+562G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202726 | ||||||
chr9:98202727
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2271+561C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202727 | ||||||
chr9:98202809
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+479C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98202809 | ||||||
chr9:98203025
|
C | A | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2271+263G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203025 | ||||||
chr9:98203068
|
C | T | 1 | a0019c0031t0001g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2271+220G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203068 | ||||||
chr9:98203069
|
G | A | 1 | a0002c0003t0001g0231 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2271+219C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203069 | ||||||
chr9:98203114
|
G | C | 1 | a0018c0029t0001g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2271+174C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203114 | ||||||
chr9:98203141
|
T | G | 12 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(9): Show | 12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2271+147A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203141 | ||||||
chr9:98203145
|
T | C | 2 | a0003c0004t0001g0314a0003c0004t0001g0315 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2271+143A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203145 | ||||||
chr9:98203169
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2271+119C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203169 | ||||||
chr9:98203190
|
C | T | 247 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(244): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2271+98G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203190 | ||||||
chr9:98203275
|
T | C | 1 | a0014c0025t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2271+13A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 10/12 | chr9 | 98203275 | ||||||
chr9:98203934
|
G | A | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2151-526C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98203934 | ||||||
chr9:98204008
|
T | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(62): Show | 71 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2151-600A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204008 | ||||||
chr9:98204170
|
TC | T | 5 | a0006c0016t0001g0048a0006c0016t0001g0049a0009c0013t0001g0023others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-763delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204170 | ||||||
chr9:98204251
|
G | T | 1 | a0005c0015t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2151-843C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204251 | ||||||
chr9:98204319
|
G | A | 1 | a0005c0010t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2151-911C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204319 | ||||||
chr9:98204358
|
C | T | 1 | a0003c0004t0001g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2151-950G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204358 | ||||||
chr9:98204388
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2151-980G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204388 | ||||||
chr9:98204426
|
C | A | 3 | a0003c0004t0001g0005a0003c0004t0001g0285a0003c0004t0001g0286 | 5 | HG02717.hp1 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-1018G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204426 | ||||||
chr9:98204509
|
C | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-1101G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204509 | ||||||
chr9:98204558
|
G | T | 29 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(26): Show | 29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2151-1150C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204558 | ||||||
chr9:98204559
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-1151C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204559 | ||||||
chr9:98204632
|
C | CA | 7 | a0005c0010t0001g0034a0005c0010t0001g0035a0005c0010t0001g0037others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2151-1225dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204632 | ||||||
chr9:98204637
|
G | A | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2151-1229C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204637 | ||||||
chr9:98204801
|
T | TG | 35 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0091others(32): Show | 38 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.2151-1394dupC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204801 | ||||||
chr9:98204883
|
A | G | 33 | a0001c0001t0001g0163a0001c0001t0001g0164a0003c0004t0001g0005others(30): Show | 35 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.2151-1475T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98204883 | ||||||
chr9:98205279
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-1871T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205279 | ||||||
chr9:98205304
|
C | G | 1 | a0002c0003t0001g0244 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2151-1896G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205304 | ||||||
chr9:98205515
|
T | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2151-2107A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205515 | ||||||
chr9:98205576
|
T | C | 10 | a0001c0001t0001g0008a0002c0003t0001g0217a0002c0003t0001g0229others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.2151-2168A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205576 | ||||||
chr9:98205578
|
A | C | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2151-2170T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205578 | ||||||
chr9:98205601
|
C | CA | 28 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(25): Show | 28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2151-2194dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205601 | ||||||
chr9:98205603
|
G | A | 28 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(25): Show | 28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2151-2195C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205603 | ||||||
chr9:98205643
|
C | A | 1 | a0016c0021t0001g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2151-2235G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205643 | ||||||
chr9:98205669
|
C | G | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2151-2261G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205669 | ||||||
chr9:98205722
|
T | C | 5 | a0002c0003t0001g0282a0002c0003t0001g0327a0002c0014t0001g0025others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2151-2314A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205722 | ||||||
chr9:98205853
|
C | T | 17 | a0002c0003t0001g0220a0002c0003t0001g0226a0002c0003t0001g0228others(14): Show | 17 | HG01106.hp1 HG01928.hp1 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.2151-2445G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205853 | ||||||
chr9:98205944
|
A | G | 1 | a0001c0002t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2151-2536T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98205944 | ||||||
chr9:98206007
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(68): Show | 77 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2151-2599G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206007 | ||||||
chr9:98206208
|
A | G | 105 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(102): Show | 112 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2150+2460T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206208 | ||||||
chr9:98206316
|
T | C | 209 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.2150+2352A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206316 | ||||||
chr9:98206321
|
A | G | 5 | a0001c0006t0001g0013a0001c0006t0001g0014a0001c0006t0001g0143others(2): Show | 7 | HG01346.hp1 HG01993.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150+2347T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206321 | ||||||
chr9:98206538
|
T | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(57): Show | 65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2150+2130A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206538 | ||||||
chr9:98206558
|
C | T | 1 | a0002c0003t0001g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2150+2110G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206558 | ||||||
chr9:98206600
|
C | T | 29 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(26): Show | 29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2150+2068G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98206600 | ||||||
chr9:98207066
|
G | A | 164 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0054others(161): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.2150+1602C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207066 | ||||||
chr9:98207201
|
T | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2150+1467A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207201 | ||||||
chr9:98207431
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2150+1237C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207431 | ||||||
chr9:98207436
|
G | A | 2 | a0001c0002t0001g0187a0001c0002t0001g0188 | 2 | NA18951.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2150+1232C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207436 | ||||||
chr9:98207468
|
T | C | 2 | a0004c0005t0001g0079a0004c0005t0001g0281 | 2 | HG00140.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2150+1200A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207468 | ||||||
chr9:98207507
|
T | C | 35 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0091others(32): Show | 38 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.2150+1161A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207507 | ||||||
chr9:98207572
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2150+1096A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207572 | ||||||
chr9:98207743
|
C | T | 2 | a0003c0026t0001g0041a0003c0034t0001g0047 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2150+925G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207743 | ||||||
chr9:98207775
|
C | T | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2150+893G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207775 | ||||||
chr9:98207811
|
C | T | 2 | a0003c0004t0001g0286a0018c0029t0001g0274 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2150+857G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207811 | ||||||
chr9:98207812
|
G | A | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150+856C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207812 | ||||||
chr9:98207854
|
C | A | 29 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(26): Show | 29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.2150+814G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207854 | ||||||
chr9:98207857
|
C | T | 2 | a0002c0014t0001g0025a0002c0014t0001g0026 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2150+811G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98207857 | ||||||
chr9:98208007
|
A | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(57): Show | 65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.2150+661T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208007 | ||||||
chr9:98208025
|
G | A | 12 | a0003c0004t0001g0057a0003c0004t0001g0283a0003c0004t0001g0287others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150+643C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208025 | ||||||
chr9:98208144
|
A | G | 12 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(9): Show | 12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150+524T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208144 | ||||||
chr9:98208278
|
C | T | 30 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(27): Show | 30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2150+390G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208278 | ||||||
chr9:98208324
|
G | A | 30 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(27): Show | 30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.2150+344C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208324 | ||||||
chr9:98208403
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150+265C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208403 | ||||||
chr9:98208443
|
G | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(68): Show | 77 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2150+225C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208443 | ||||||
chr9:98208455
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2150+213G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208455 | ||||||
chr9:98208568
|
C | CA | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150+99_2150+100in others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208568 | ||||||
chr9:98208568
|
C | CG | 226 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(223): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.2150+99_2150+100in others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208568 | ||||||
chr9:98208570
|
T | A | 1 | a0013c0041t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2150+98A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208570 | ||||||
chr9:98208574
|
A | T | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2150+94T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208574 | ||||||
chr9:98208599
|
A | G | 238 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(235): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.2150+69T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208599 | ||||||
chr9:98208643
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2150+25G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 9/12 | chr9 | 98208643 | ||||||
chr9:98209234
|
C | A | 1 | a0013c0041t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-90G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209234 | ||||||
chr9:98209254
|
G | A | 5 | a0006c0016t0001g0048a0006c0016t0001g0049a0009c0013t0001g0023others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-110C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209254 | ||||||
chr9:98209387
|
G | C | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1674-243C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209387 | ||||||
chr9:98209454
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1674-310C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209454 | ||||||
chr9:98209538
|
G | A | 1 | a0003c0004t0001g0283 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1674-394C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209538 | ||||||
chr9:98209618
|
T | A | 1 | a0013c0041t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-474A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209618 | ||||||
chr9:98209624
|
A | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1674-480T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209624 | ||||||
chr9:98209703
|
C | A | 5 | a0006c0016t0001g0048a0006c0016t0001g0049a0009c0013t0001g0023others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-559G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209703 | ||||||
chr9:98209710
|
CT | C | 14 | a0002c0003t0001g0327a0003c0004t0001g0045a0003c0004t0001g0102others(11): Show | 14 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1674-567delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209710 | ||||||
chr9:98209718
|
TTTCC | T | 7 | a0001c0001t0001g0215a0003c0004t0001g0057a0003c0004t0001g0285others(4): Show | 7 | HG02615.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-578_1674-575d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209718 | ||||||
chr9:98209730
|
C | CTTCTTTC others(2): Show |
83 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1674-587_1674-586i others(11): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209730 | ||||||
chr9:98209730
|
C | T | 1 | a0004c0005t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1674-586G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209730 | ||||||
chr9:98209734
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0053others(25): Show | 33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-590G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209734 | ||||||
chr9:98209738
|
T | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1674-594A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209738 | ||||||
chr9:98209741
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0053others(25): Show | 33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-597G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209741 | ||||||
chr9:98209743
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0053others(25): Show | 33 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1674-599A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209743 | ||||||
chr9:98209751
|
C | CT | 23 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0060others(20): Show | 26 | HG00408.hp1 HG00558.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1674-608dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209751 | ||||||
chr9:98209754
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0105others(2): Show | 7 | HG02132.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-610G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209754 | ||||||
chr9:98209755
|
CT | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0061others(23): Show | 27 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1674-612delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209755 | ||||||
chr9:98209756
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0105others(2): Show | 7 | HG02132.hp1 HG02717.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-612A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCC | 50 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(47): Show | 56 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCCCTTC others(25): Show |
1 | a0002c0003t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1674-613_1674-612i others(34): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCCTTCC | 18 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0081others(15): Show | 18 | HG00438.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCCTTCC others(4): Show |
6 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0117others(3): Show | 6 | HG00140.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCCTTCC others(8): Show |
5 | a0001c0001t0001g0214a0002c0003t0001g0229a0002c0003t0001g0232others(2): Show | 5 | HG00733.hp1 HG02015.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-613_1674-612i others(17): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTCCTTCC others(12): Show |
2 | a0003c0004t0001g0320a0003c0004t0001g0321 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1674-613_1674-612i others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCC | 15 | a0001c0001t0001g0151a0001c0001t0001g0210a0001c0008t0001g0125others(12): Show | 17 | HG00323.hp2 HG00597.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1674-616_1674-613d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(1): Show |
8 | a0001c0001t0001g0211a0001c0001t0001g0212a0002c0003t0001g0327others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1674-620_1674-613d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(5): Show |
4 | a0001c0001t0001g0169a0003c0004t0001g0102a0003c0034t0001g0047others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-624_1674-613d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(9): Show |
2 | a0014c0025t0001g0039a0018c0029t0001g0274 | 2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1674-628_1674-613d others(18): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(13): Show |
4 | a0002c0003t0001g0247a0003c0004t0001g0045a0003c0009t0001g0040others(1): Show | 4 | HG01081.hp1 HG01516.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-632_1674-613d others(22): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(17): Show |
3 | a0001c0001t0001g0104a0001c0001t0001g0111a0003c0004t0003g0046 | 3 | HG01891.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1674-636_1674-613d others(26): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
T | TTTCCTTC others(29): Show |
1 | a0001c0002t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1674-648_1674-613d others(38): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
TTTCC | T | 88 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0141others(85): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1674-616_1674-613d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
TTTCCTTC others(1): Show |
T | 3 | a0001c0002t0001g0093a0001c0002t0001g0150a0010c0020t0001g0336 | 3 | HG01069.hp2 HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1674-620_1674-613d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209756
|
TTTCCTTC others(5): Show |
T | 2 | a0009c0013t0001g0023a0009c0013t0001g0024 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1674-624_1674-613d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209756 | ||||||
chr9:98209758
|
T | C | 30 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0077others(27): Show | 30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1674-614A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209758 | ||||||
chr9:98209793
|
T | TCCTTCCT others(7): Show |
1 | a0013c0041t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1674-650_1674-649i others(16): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209793 | ||||||
chr9:98209795
|
T | C | 2 | a0001c0001t0001g0069a0018c0029t0001g0274 | 2 | HG03098.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1674-651A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209795 | ||||||
chr9:98209880
|
C | G | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1674-736G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209880 | ||||||
chr9:98209929
|
A | G | 1 | a0001c0002t0001g0324 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1673+727T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209929 | ||||||
chr9:98209940
|
CACCT | C | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1673+712_1673+715d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209940 | ||||||
chr9:98209950
|
TTCCGA | T | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1673+701_1673+705d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209950 | ||||||
chr9:98209963
|
G | T | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+693C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209963 | ||||||
chr9:98209973
|
C | T | 12 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(9): Show | 12 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1673+683G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209973 | ||||||
chr9:98209990
|
C | CT | 7 | a0001c0002t0001g0190a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1673+665dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | ||||||
chr9:98209990
|
CT | C | 37 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(34): Show | 37 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1673+665delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | ||||||
chr9:98209990
|
CTTT | C | 11 | a0001c0001t0001g0008a0002c0003t0001g0217a0002c0003t0001g0229others(8): Show | 12 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.1673+663_1673+665d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209990 | ||||||
chr9:98209993
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(117): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1673+663A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209993 | ||||||
chr9:98209994
|
T | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(2): Show | 5 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+662A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98209994 | ||||||
chr9:98210022
|
C | T | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1673+634G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210022 | ||||||
chr9:98210106
|
A | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(231): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1673+550T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210106 | ||||||
chr9:98210268
|
C | T | 1 | a0003c0004t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1673+388G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210268 | ||||||
chr9:98210269
|
A | C | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+387T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210269 | ||||||
chr9:98210299
|
T | C | 1 | a0023c0023t0001g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1673+357A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210299 | ||||||
chr9:98210318
|
G | A | 3 | a0002c0003t0001g0222a0002c0003t0001g0223a0002c0003t0001g0265 | 3 | NA18947.hp1 NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1673+338C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210318 | ||||||
chr9:98210326
|
T | C | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1673+330A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210326 | ||||||
chr9:98210367
|
T | G | 1 | a0003c0012t0001g0284 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1673+289A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210367 | ||||||
chr9:98210403
|
G | T | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1673+253C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210403 | ||||||
chr9:98210417
|
T | C | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1673+239A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210417 | ||||||
chr9:98210451
|
G | A | 2 | a0006c0016t0001g0048a0006c0016t0001g0049 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1673+205C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210451 | ||||||
chr9:98210463
|
T | A | 1 | a0002c0003t0001g0226 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1673+193A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210463 | ||||||
chr9:98210471
|
T | C | 1 | a0008c0018t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1673+185A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210471 | ||||||
chr9:98210628
|
C | T | 1 | a0002c0003t0001g0229 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1673+28G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 8/12 | chr9 | 98210628 | ||||||
chr9:98210896
|
A | AGAGGCCT | 228 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(225): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1486-60_1486-54dup others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98210896 | ||||||
chr9:98211048
|
G | A | 17 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(14): Show | 17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1486-205C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211048 | ||||||
chr9:98211140
|
C | T | 1 | a0003c0004t0001g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1486-297G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211140 | ||||||
chr9:98211253
|
C | T | 2 | a0008c0018t0001g0075a0008c0018t0001g0076 | 2 | HG01071.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1486-410G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211253 | ||||||
chr9:98211376
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0169a0001c0001t0001g0210others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1486-533G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211376 | ||||||
chr9:98211505
|
T | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1486-662A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211505 | ||||||
chr9:98211512
|
C | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1486-669G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211512 | ||||||
chr9:98211550
|
T | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(57): Show | 65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1486-707A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211550 | ||||||
chr9:98211570
|
T | A | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-727A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211570 | ||||||
chr9:98211618
|
T | C | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-775A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211618 | ||||||
chr9:98211619
|
G | T | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-776C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211619 | ||||||
chr9:98211800
|
C | CT | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 103 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1486-958dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211800 | ||||||
chr9:98211861
|
G | A | 1 | a0001c0002t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1486-1018C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211861 | ||||||
chr9:98211909
|
T | A | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1486-1066A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211909 | ||||||
chr9:98211954
|
C | T | 4 | a0003c0011t0001g0029a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-1111G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98211954 | ||||||
chr9:98212061
|
C | T | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1485+1047G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212061 | ||||||
chr9:98212062
|
G | A | 27 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(24): Show | 28 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.1485+1046C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212062 | ||||||
chr9:98212088
|
C | T | 1 | a0001c0019t0001g0173 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1485+1020G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212088 | ||||||
chr9:98212163
|
C | A | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1485+945G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212163 | ||||||
chr9:98212253
|
G | T | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1485+855C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212253 | ||||||
chr9:98212260
|
T | G | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1485+848A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212260 | ||||||
chr9:98212394
|
T | C | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1485+714A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212394 | ||||||
chr9:98212474
|
G | A | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1485+634C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212474 | ||||||
chr9:98212480
|
C | T | 4 | a0001c0001t0001g0183a0002c0003t0001g0224a0002c0003t0001g0251others(1): Show | 4 | HG00639.hp1 HG01496.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1485+628G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212480 | ||||||
chr9:98212506
|
C | CT | 149 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(146): Show | 162 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1485+601dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212506 | ||||||
chr9:98212506
|
CT | C | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1485+601delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212506 | ||||||
chr9:98212705
|
C | T | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1485+403G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212705 | ||||||
chr9:98212788
|
G | A | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1485+320C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212788 | ||||||
chr9:98212801
|
G | C | 1 | a0014c0025t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1485+307C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98212801 | ||||||
chr9:98213036
|
C | T | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1485+72G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213036 | ||||||
chr9:98213072
|
G | T | 1 | a0018c0029t0001g0274 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+36C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213072 | ||||||
chr9:98213076
|
G | A | 5 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0307others(2): Show | 5 | HG00323.hp1 HG00642.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+32C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 7/12 | chr9 | 98213076 | ||||||
chr9:98213266
|
C | T | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1375-48G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213266 | ||||||
chr9:98213311
|
T | G | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-93A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213311 | ||||||
chr9:98213412
|
G | A | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-194C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213412 | ||||||
chr9:98213555
|
A | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1375-337T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213555 | ||||||
chr9:98213582
|
C | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-364G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213582 | ||||||
chr9:98213804
|
A | G | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1375-586T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213804 | ||||||
chr9:98213849
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0117 | 2 | NA18941.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1375-631A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213849 | ||||||
chr9:98213958
|
A | G | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1375-740T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98213958 | ||||||
chr9:98214059
|
C | T | 5 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1375-841G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214059 | ||||||
chr9:98214160
|
A | C | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-942T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214160 | ||||||
chr9:98214190
|
ATGGCCAG others(133): Show |
A | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(63): Show | 74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1375-1112_1375-973 others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214190 | ||||||
chr9:98214198
|
GTTGATTT others(63): Show |
G | 58 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(55): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1375-1050_1375-981 others(73): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214198 | ||||||
chr9:98214234
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1375-1016C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214234 | ||||||
chr9:98214256
|
C | T | 9 | a0001c0008t0001g0122a0001c0008t0001g0123a0001c0008t0001g0124others(6): Show | 9 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1375-1038G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214256 | ||||||
chr9:98214257
|
G | A | 1 | a0001c0002t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1375-1039C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214257 | ||||||
chr9:98214268
|
A | G | 27 | a0001c0001t0001g0163a0001c0001t0001g0164a0003c0004t0001g0297others(24): Show | 27 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.1375-1050T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | ||||||
chr9:98214268
|
ATTGATTT others(63): Show |
A | 73 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1375-1120_1375-105 others(74): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | ||||||
chr9:98214268
|
ATTGATTT others(133): Show |
A | 2 | a0009c0013t0001g0023a0009c0013t0001g0024 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1375-1190_1375-105 others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214268 | ||||||
chr9:98214277
|
GAAATGAA others(134): Show |
G | 1 | a0022c0033t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1375-1200_1375-106 others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214277 | ||||||
chr9:98214396
|
C | T | 29 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(26): Show | 29 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1375-1178G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214396 | ||||||
chr9:98214530
|
T | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1375-1312A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214530 | ||||||
chr9:98214536
|
C | G | 42 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1375-1318G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214536 | ||||||
chr9:98214537
|
G | A | 10 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-1319C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214537 | ||||||
chr9:98214548
|
GTTGATTT others(63): Show |
G | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1375-1400_1375-133 others(74): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214548 | ||||||
chr9:98214583
|
C | T | 1 | a0003c0004t0001g0317 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1375-1365G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214583 | ||||||
chr9:98214592
|
A | G | 76 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(73): Show | 77 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1375-1374T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214592 | ||||||
chr9:98214607
|
G | A | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-1389C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214607 | ||||||
chr9:98214610
|
G | A | 3 | a0001c0001t0001g0073a0002c0003t0001g0218a0002c0003t0001g0219 | 3 | HG01099.hp1 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1375-1392C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214610 | ||||||
chr9:98214665
|
C | T | 17 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(14): Show | 17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-1447G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214665 | ||||||
chr9:98214838
|
G | T | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-1620C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214838 | ||||||
chr9:98214857
|
T | A | 4 | a0003c0004t0001g0320a0003c0004t0001g0321a0003c0004t0001g0322others(1): Show | 4 | HG02809.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-1639A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214857 | ||||||
chr9:98214857
|
T | C | 83 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1375-1639A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98214857 | ||||||
chr9:98215072
|
A | C | 1 | a0001c0002t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1375-1854T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215072 | ||||||
chr9:98215110
|
C | T | 239 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1375-1892G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215110 | ||||||
chr9:98215175
|
T | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1375-1957A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215175 | ||||||
chr9:98215225
|
G | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-2007C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215225 | ||||||
chr9:98215355
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1375-2137C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215355 | ||||||
chr9:98215484
|
T | A | 2 | a0002c0003t0001g0020a0004c0005t0001g0078 | 3 | HG01346.hp2 HG02300.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1375-2266A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215484 | ||||||
chr9:98215492
|
A | G | 1 | a0002c0003t0001g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1375-2274T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215492 | ||||||
chr9:98215592
|
C | T | 11 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(8): Show | 11 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-2374G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215592 | ||||||
chr9:98215757
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1375-2539G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215757 | ||||||
chr9:98215801
|
T | C | 49 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(46): Show | 49 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1375-2583A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215801 | ||||||
chr9:98215949
|
C | A | 1 | a0006c0016t0001g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1375-2731G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98215949 | ||||||
chr9:98216012
|
A | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1375-2794T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216012 | ||||||
chr9:98216094
|
C | T | 17 | a0003c0004t0001g0045a0003c0004t0001g0102a0003c0009t0001g0040others(14): Show | 17 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-2876G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216094 | ||||||
chr9:98216172
|
G | T | 10 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG00323.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-2954C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216172 | ||||||
chr9:98216260
|
G | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1375-3042C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216260 | ||||||
chr9:98216261
|
T | A | 1 | a0002c0003t0001g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1375-3043A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216261 | ||||||
chr9:98216344
|
G | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1375-3126C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216344 | ||||||
chr9:98216380
|
C | T | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1375-3162G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216380 | ||||||
chr9:98216381
|
G | T | 44 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1375-3163C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216381 | ||||||
chr9:98216440
|
G | A | 1 | a0001c0008t0001g0123 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1375-3222C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216440 | ||||||
chr9:98216450
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1375-3232A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216450 | ||||||
chr9:98216608
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1375-3390G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216608 | ||||||
chr9:98216620
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-3402G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216620 | ||||||
chr9:98216901
|
T | A | 2 | a0002c0003t0001g0231a0002c0003t0001g0238 | 2 | NA18612.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1375-3683A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216901 | ||||||
chr9:98216988
|
G | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(71): Show | 75 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1375-3770C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98216988 | ||||||
chr9:98217061
|
T | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1374+3772A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217061 | ||||||
chr9:98217063
|
T | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(237): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1374+3770A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217063 | ||||||
chr9:98217203
|
G | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(90): Show | 101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1374+3630C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217203 | ||||||
chr9:98217211
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1374+3622T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217211 | ||||||
chr9:98217232
|
G | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1374+3601C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217232 | ||||||
chr9:98217309
|
G | A | 2 | a0002c0003t0001g0254a0002c0003t0001g0255 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+3524C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217309 | ||||||
chr9:98217314
|
T | C | 2 | a0002c0014t0001g0025a0002c0014t0001g0026 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1374+3519A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217314 | ||||||
chr9:98217392
|
G | A | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+3441C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217392 | ||||||
chr9:98217447
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1374+3386G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217447 | ||||||
chr9:98217480
|
G | A | 31 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(28): Show | 31 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.1374+3353C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217480 | ||||||
chr9:98217520
|
G | C | 2 | a0002c0003t0001g0254a0002c0003t0001g0255 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+3313C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217520 | ||||||
chr9:98217774
|
G | A | 61 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(58): Show | 66 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.1374+3059C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217774 | ||||||
chr9:98217810
|
G | A | 1 | a0001c0008t0001g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1374+3023C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98217810 | ||||||
chr9:98218024
|
A | C | 2 | a0002c0003t0001g0254a0002c0003t0001g0255 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1374+2809T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218024 | ||||||
chr9:98218024
|
A | T | 141 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0054others(138): Show | 147 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1374+2809T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218024 | ||||||
chr9:98218033
|
T | C | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+2800A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218033 | ||||||
chr9:98218246
|
G | A | 2 | a0005c0015t0001g0030a0005c0015t0001g0031 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1374+2587C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218246 | ||||||
chr9:98218410
|
C | CA | 147 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0054others(144): Show | 153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1374+2422dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218410 | ||||||
chr9:98218484
|
G | A | 5 | a0006c0016t0001g0048a0006c0016t0001g0049a0009c0013t0001g0023others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+2349C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218484 | ||||||
chr9:98218521
|
C | A | 60 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(57): Show | 65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1374+2312G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218521 | ||||||
chr9:98218562
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1374+2271C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218562 | ||||||
chr9:98218583
|
A | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(57): Show | 65 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1374+2250T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218583 | ||||||
chr9:98218630
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1374+2203G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218630 | ||||||
chr9:98218650
|
A | G | 1 | a0002c0003t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1374+2183T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218650 | ||||||
chr9:98218691
|
T | C | 156 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0054others(153): Show | 162 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1374+2142A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218691 | ||||||
chr9:98218746
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1374+2087T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218746 | ||||||
chr9:98218823
|
C | T | 5 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0069others(2): Show | 5 | NA18941.hp2 NA18951.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374+2010G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218823 | ||||||
chr9:98218824
|
G | A | 1 | a0010c0020t0001g0335 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1374+2009C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218824 | ||||||
chr9:98218860
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1374+1973G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218860 | ||||||
chr9:98218877
|
C | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+1956G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98218877 | ||||||
chr9:98219099
|
C | T | 2 | a0003c0004t0001g0307a0003c0004t0001g0316 | 2 | HG00642.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1374+1734G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219099 | ||||||
chr9:98219100
|
G | C | 1 | a0001c0002t0001g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1374+1733C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219100 | ||||||
chr9:98219127
|
T | C | 1 | a0003c0004t0001g0311 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1374+1706A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219127 | ||||||
chr9:98219161
|
C | T | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+1672G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219161 | ||||||
chr9:98219475
|
T | G | 147 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0054others(144): Show | 153 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1374+1358A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219475 | ||||||
chr9:98219575
|
G | A | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1374+1258C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219575 | ||||||
chr9:98219587
|
A | T | 2 | a0003c0004t0001g0311a0003c0004t0001g0312 | 2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1374+1246T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219587 | ||||||
chr9:98219621
|
G | A | 5 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00323.hp2 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+1212C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219621 | ||||||
chr9:98219624
|
C | T | 11 | a0001c0001t0001g0169a0001c0001t0001g0210a0001c0001t0001g0211others(8): Show | 11 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1374+1209G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219624 | ||||||
chr9:98219833
|
G | A | 1 | a0004c0005t0001g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1374+1000C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98219833 | ||||||
chr9:98220165
|
G | A | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1374+668C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220165 | ||||||
chr9:98220187
|
C | A | 1 | a0001c0002t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1374+646G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220187 | ||||||
chr9:98220277
|
G | A | 2 | a0002c0003t0001g0282a0002c0003t0001g0327 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1374+556C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220277 | ||||||
chr9:98220321
|
A | G | 1 | a0014c0025t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1374+512T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220321 | ||||||
chr9:98220549
|
T | G | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1374+284A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220549 | ||||||
chr9:98220576
|
T | C | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1374+257A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220576 | ||||||
chr9:98220676
|
A | G | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1374+157T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220676 | ||||||
chr9:98220743
|
A | G | 2 | a0001c0019t0001g0172a0001c0019t0001g0173 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1374+90T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220743 | ||||||
chr9:98220766
|
C | T | 2 | a0006c0016t0001g0048a0006c0016t0001g0049 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1374+67G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220766 | ||||||
chr9:98220798
|
G | A | 5 | a0003c0004t0001g0301a0003c0004t0001g0302a0003c0004t0001g0307others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+35C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 6/12 | chr9 | 98220798 | ||||||
chr9:98221284
|
C | G | 232 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.979-56G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221284 | ||||||
chr9:98221322
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.979-94C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221322 | ||||||
chr9:98221544
|
C | G | 88 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(85): Show | 96 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.979-316G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221544 | ||||||
chr9:98221603
|
C | T | 1 | a0017c0027t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-375G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221603 | ||||||
chr9:98221787
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0213 | 2 | NA18960.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.979-559C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221787 | ||||||
chr9:98221909
|
T | G | 61 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(58): Show | 69 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.979-681A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221909 | ||||||
chr9:98221929
|
C | G | 1 | a0004c0005t0001g0279 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.979-701G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221929 | ||||||
chr9:98221943
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.979-715C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98221943 | ||||||
chr9:98222137
|
T | C | 1 | a0017c0027t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-909A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222137 | ||||||
chr9:98222549
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.979-1321C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222549 | ||||||
chr9:98222573
|
C | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(59): Show | 70 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.979-1345G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222573 | ||||||
chr9:98222622
|
G | A | 1 | a0002c0003t0001g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.979-1394C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222622 | ||||||
chr9:98222664
|
T | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.979-1436A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222664 | ||||||
chr9:98222703
|
C | G | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.979-1475G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222703 | ||||||
chr9:98222708
|
C | T | 1 | a0006c0016t0001g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979-1480G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98222708 | ||||||
chr9:98223029
|
C | T | 58 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0073others(55): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.979-1801G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223029 | ||||||
chr9:98223030
|
G | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.979-1802C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223030 | ||||||
chr9:98223085
|
T | A | 28 | a0001c0001t0001g0054a0001c0001t0001g0077a0001c0001t0001g0082others(25): Show | 28 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-1857A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223085 | ||||||
chr9:98223105
|
C | T | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223105 | ||||||
chr9:98223106
|
A | G | 108 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0056others(105): Show | 116 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.979-1878T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223106 | ||||||
chr9:98223304
|
A | G | 60 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(57): Show | 66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.979-2076T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223304 | ||||||
chr9:98223428
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.979-2200G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223428 | ||||||
chr9:98223445
|
T | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.979-2217A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223445 | ||||||
chr9:98223544
|
T | G | 10 | a0001c0001t0001g0008a0002c0003t0001g0217a0002c0003t0001g0229others(7): Show | 11 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.979-2316A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223544 | ||||||
chr9:98223608
|
A | G | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.979-2380T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223608 | ||||||
chr9:98223640
|
GAGTT | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.979-2416_979-2413d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223640 | ||||||
chr9:98223789
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.979-2561G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223789 | ||||||
chr9:98223884
|
C | A | 6 | a0003c0004t0001g0057a0003c0004t0001g0287a0003c0004t0001g0296others(3): Show | 6 | HG02615.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-2656G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223884 | ||||||
chr9:98223918
|
G | A | 1 | a0017c0027t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979-2690C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223918 | ||||||
chr9:98223921
|
C | T | 1 | a0016c0021t0001g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979-2693G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223921 | ||||||
chr9:98223974
|
C | T | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-2746G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98223974 | ||||||
chr9:98224015
|
T | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.979-2787A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224015 | ||||||
chr9:98224060
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.979-2832G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224060 | ||||||
chr9:98224072
|
T | C | 3 | a0001c0002t0001g0332a0001c0002t0001g0333a0001c0002t0001g0334 | 3 | NA18966.hp2 NA18967.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.979-2844A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224072 | ||||||
chr9:98224154
|
A | G | 7 | a0005c0010t0001g0034a0005c0010t0001g0035a0005c0010t0001g0037others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-2926T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224154 | ||||||
chr9:98224166
|
T | C | 7 | a0005c0010t0001g0034a0005c0010t0001g0035a0005c0010t0001g0037others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-2938A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224166 | ||||||
chr9:98224176
|
G | A | 1 | a0001c0001t0001g0007 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.979-2948C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224176 | ||||||
chr9:98224183
|
C | T | 5 | a0001c0002t0001g0152a0001c0002t0001g0154a0001c0002t0001g0155others(2): Show | 5 | HG00544.hp2 HG02074.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-2955G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224183 | ||||||
chr9:98224207
|
A | G | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.979-2979T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224207 | ||||||
chr9:98224210
|
AG | A | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.979-2983delC | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224210 | ||||||
chr9:98224218
|
A | AAAG | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-2993_979-2991d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224218 | ||||||
chr9:98224265
|
GT | G | 152 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.979-3038delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224265 | ||||||
chr9:98224275
|
CTTTTCTT others(12): Show |
C | 1 | a0003c0004t0001g0283 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.979-3066_979-3048d others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224275 | ||||||
chr9:98224280
|
C | CT | 57 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0062others(54): Show | 59 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-3053dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | ||||||
chr9:98224280
|
CT | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0106others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.979-3053delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | ||||||
chr9:98224280
|
CTTT | C | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3055_979-3053d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224280 | ||||||
chr9:98224285
|
T | C | 2 | a0002c0003t0001g0221a0012c0040t0001g0147 | 2 | HG00597.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.979-3057A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224285 | ||||||
chr9:98224374
|
C | A | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3146G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224374 | ||||||
chr9:98224411
|
T | C | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-3183A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224411 | ||||||
chr9:98224565
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.979-3337C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224565 | ||||||
chr9:98224722
|
G | A | 1 | a0003c0004t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.979-3494C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224722 | ||||||
chr9:98224908
|
C | A | 5 | a0002c0003t0001g0217a0002c0003t0001g0229a0002c0003t0001g0249others(2): Show | 5 | HG00733.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-3680G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98224908 | ||||||
chr9:98225085
|
C | T | 3 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331 | 3 | NA18959.hp2 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.979-3857G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225085 | ||||||
chr9:98225172
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.978+3780C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225172 | ||||||
chr9:98225265
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 6 | HG00639.hp2 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+3687C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225265 | ||||||
chr9:98225340
|
A | G | 145 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(142): Show | 157 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.978+3612T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225340 | ||||||
chr9:98225434
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.978+3518T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225434 | ||||||
chr9:98225444
|
T | C | 4 | a0002c0003t0001g0282a0002c0003t0001g0327a0017c0027t0001g0275others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+3508A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225444 | ||||||
chr9:98225561
|
C | A | 329 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(326): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.978+3391G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225561 | ||||||
chr9:98225608
|
T | C | 146 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(143): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3344A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225608 | ||||||
chr9:98225635
|
G | C | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+3317C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225635 | ||||||
chr9:98225642
|
T | C | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+3310A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225642 | ||||||
chr9:98225735
|
G | A | 1 | a0019c0031t0001g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.978+3217C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225735 | ||||||
chr9:98225785
|
T | C | 146 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(143): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+3167A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225785 | ||||||
chr9:98225874
|
G | A | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+3078C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225874 | ||||||
chr9:98225882
|
C | T | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.978+3070G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225882 | ||||||
chr9:98225925
|
T | A | 3 | a0003c0009t0001g0032a0005c0015t0001g0030a0005c0015t0001g0031 | 3 | HG01884.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.978+3027A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98225925 | ||||||
chr9:98226071
|
C | A | 3 | a0001c0002t0001g0187a0001c0002t0001g0188a0001c0002t0001g0190 | 3 | NA18951.hp1 NA18953.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.978+2881G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226071 | ||||||
chr9:98226195
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(37): Show | 43 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+2757C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226195 | ||||||
chr9:98226220
|
T | C | 2 | a0006c0016t0001g0048a0006c0016t0001g0049 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.978+2732A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226220 | ||||||
chr9:98226228
|
G | A | 146 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(143): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.978+2724C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226228 | ||||||
chr9:98226264
|
C | T | 1 | a0006c0038t0001g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.978+2688G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226264 | ||||||
chr9:98226303
|
C | T | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2649G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226303 | ||||||
chr9:98226317
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.978+2635C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226317 | ||||||
chr9:98226365
|
A | G | 1 | a0002c0003t0001g0242 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.978+2587T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226365 | ||||||
chr9:98226393
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2559C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226393 | ||||||
chr9:98226527
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.978+2425A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226527 | ||||||
chr9:98226630
|
G | A | 1 | a0002c0003t0001g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.978+2322C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226630 | ||||||
chr9:98226679
|
T | C | 4 | a0002c0003t0001g0282a0002c0003t0001g0327a0017c0027t0001g0275others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2273A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226679 | ||||||
chr9:98226907
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+2045C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226907 | ||||||
chr9:98226922
|
G | A | 1 | a0001c0002t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.978+2030C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226922 | ||||||
chr9:98226987
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.978+1965A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98226987 | ||||||
chr9:98227166
|
T | G | 1 | a0017c0027t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+1786A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227166 | ||||||
chr9:98227284
|
G | A | 1 | a0002c0003t0001g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.978+1668C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227284 | ||||||
chr9:98227355
|
C | T | 1 | a0003c0004t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+1597G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227355 | ||||||
chr9:98227400
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+1552G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227400 | ||||||
chr9:98227485
|
G | A | 1 | a0003c0004t0001g0292 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.978+1467C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227485 | ||||||
chr9:98227554
|
C | T | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978+1398G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227554 | ||||||
chr9:98227614
|
A | AC | 147 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.978+1337dupG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227614 | ||||||
chr9:98227781
|
CA | C | 123 | a0001c0001t0001g0214a0002c0003t0001g0016a0002c0003t0001g0017others(120): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.978+1170delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227781 | ||||||
chr9:98227781
|
CAA | C | 16 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0220others(13): Show | 19 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+1169_978+1170d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98227781 | ||||||
chr9:98228012
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+940C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228012 | ||||||
chr9:98228075
|
C | T | 1 | a0003c0004t0001g0315 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978+877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228075 | ||||||
chr9:98228298
|
A | C | 63 | a0003c0004t0001g0005a0003c0004t0001g0045a0003c0004t0001g0057others(60): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.978+654T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228298 | ||||||
chr9:98228571
|
G | A | 81 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(78): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.978+381C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228571 | ||||||
chr9:98228603
|
C | T | 1 | a0001c0002t0001g0152 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.978+349G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228603 | ||||||
chr9:98228631
|
A | C | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978+321T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228631 | ||||||
chr9:98228702
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.978+250A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228702 | ||||||
chr9:98228815
|
T | C | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.978+137A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228815 | ||||||
chr9:98228820
|
A | C | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+132T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 5/12 | chr9 | 98228820 | ||||||
chr9:98229572
|
A | C | 2 | a0006c0016t0001g0048a0006c0016t0001g0049 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.782-424T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229572 | ||||||
chr9:98229654
|
G | A | 1 | a0005c0010t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.782-506C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229654 | ||||||
chr9:98229655
|
C | A | 1 | a0005c0010t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.782-507G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229655 | ||||||
chr9:98229936
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0119others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-788C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229936 | ||||||
chr9:98229944
|
C | T | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.782-796G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98229944 | ||||||
chr9:98230247
|
GA | G | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.782-1100delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230247 | ||||||
chr9:98230334
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.782-1186G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230334 | ||||||
chr9:98230413
|
C | T | 147 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.782-1265G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230413 | ||||||
chr9:98230540
|
G | T | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.782-1392C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230540 | ||||||
chr9:98230612
|
C | T | 7 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-1464G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230612 | ||||||
chr9:98230651
|
G | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(45): Show | 51 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.782-1503C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230651 | ||||||
chr9:98230740
|
C | CT | 237 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.782-1593_782-1592i others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230740 | ||||||
chr9:98230829
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.782-1681G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230829 | ||||||
chr9:98230963
|
C | T | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.782-1815G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98230963 | ||||||
chr9:98231033
|
T | C | 1 | a0002c0003t0001g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.782-1885A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231033 | ||||||
chr9:98231171
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.782-2023T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231171 | ||||||
chr9:98231178
|
C | T | 67 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(64): Show | 74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.782-2030G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231178 | ||||||
chr9:98231279
|
C | CT | 73 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0054others(70): Show | 77 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.782-2132dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231279
|
C | CTT | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0050others(28): Show | 33 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.782-2133_782-2132d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231279
|
C | CTTT | 42 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0198others(39): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.781+2134_782-2132d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231279
|
C | CTTTT | 8 | a0003c0004t0001g0057a0003c0004t0001g0286a0003c0004t0001g0300others(5): Show | 8 | HG01109.hp2 HG02723.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.781+2133_782-2132d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231279
|
CT | C | 51 | a0001c0001t0001g0213a0001c0002t0001g0128a0002c0003t0001g0004others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.782-2132delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231279
|
CTTTTTTT others(2): Show |
C | 12 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.781+2128_782-2132d others(11): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231279 | ||||||
chr9:98231325
|
T | C | 1 | a0002c0003t0001g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.781+2091A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231325 | ||||||
chr9:98231391
|
T | C | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.781+2025A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231391 | ||||||
chr9:98231419
|
C | G | 1 | a0009c0013t0001g0023 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.781+1997G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231419 | ||||||
chr9:98231687
|
T | C | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1729A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231687 | ||||||
chr9:98231705
|
C | T | 1 | a0002c0003t0001g0232 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781+1711G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231705 | ||||||
chr9:98231707
|
T | C | 14 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(11): Show | 14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.781+1709A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98231707 | ||||||
chr9:98232176
|
A | T | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781+1240T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232176 | ||||||
chr9:98232188
|
G | A | 67 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(64): Show | 74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.781+1228C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232188 | ||||||
chr9:98232194
|
G | C | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+1222C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232194 | ||||||
chr9:98232227
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.781+1189C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232227 | ||||||
chr9:98232236
|
G | A | 2 | a0003c0011t0001g0029a0003c0034t0001g0047 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.781+1180C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232236 | ||||||
chr9:98232340
|
C | CTGTTTTT others(5): Show |
2 | a0002c0003t0001g0231a0018c0029t0001g0274 | 2 | HG03098.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.781+1064_781+1075d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232340 | ||||||
chr9:98232342
|
G | GT | 7 | a0001c0001t0001g0070a0001c0001t0001g0204a0001c0001t0001g0212others(4): Show | 7 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+1073dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTGTTTTT others(11): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18985.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(20): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(6): Show |
1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+1073_781+1074i others(15): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(7): Show |
9 | a0003c0009t0001g0033a0003c0009t0001g0036a0003c0009t0001g0040others(6): Show | 9 | HG01255.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(16): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(8): Show |
3 | a0003c0009t0001g0032a0005c0015t0001g0030a0005c0015t0001g0031 | 3 | HG01884.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(17): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(9): Show |
12 | a0003c0004t0001g0045a0003c0004t0001g0303a0003c0004t0001g0315others(9): Show | 12 | HG01081.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(18): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(10): Show |
39 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0061others(36): Show | 41 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(19): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(11): Show |
59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 65 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(20): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(12): Show |
22 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0067others(19): Show | 22 | HG01099.hp2 HG01109.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+1073_781+1074i others(21): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232342
|
G | GTTTTTTT others(13): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0088 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.781+1073_781+1074i others(22): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232342 | ||||||
chr9:98232343
|
T | TTTTTTTT others(4): Show |
79 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(76): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.781+1062_781+1072d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232343 | ||||||
chr9:98232343
|
T | TTTTTTTT others(5): Show |
1 | a0002c0003t0001g0230 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.781+1072_781+1073i others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232343 | ||||||
chr9:98232360
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.781+1056C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232360 | ||||||
chr9:98232368
|
C | T | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+1048G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232368 | ||||||
chr9:98232385
|
T | C | 44 | a0003c0004t0001g0005a0003c0004t0001g0057a0003c0004t0001g0102others(41): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.781+1031A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232385 | ||||||
chr9:98232394
|
A | G | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.781+1022T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232394 | ||||||
chr9:98232441
|
T | C | 147 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.781+975A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232441 | ||||||
chr9:98232490
|
T | A | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.781+926A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232490 | ||||||
chr9:98232521
|
T | C | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.781+895A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232521 | ||||||
chr9:98232614
|
A | G | 65 | a0003c0004t0001g0005a0003c0004t0001g0045a0003c0004t0001g0057others(62): Show | 67 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.781+802T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232614 | ||||||
chr9:98232799
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.781+617A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98232799 | ||||||
chr9:98233059
|
G | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+357C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233059 | ||||||
chr9:98233169
|
A | G | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+247T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233169 | ||||||
chr9:98233188
|
T | C | 2 | a0001c0002t0001g0145a0001c0002t0001g0146 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.781+228A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233188 | ||||||
chr9:98233252
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781+164G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233252 | ||||||
chr9:98233263
|
G | A | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781+153C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233263 | ||||||
chr9:98233267
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG02683.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+149G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233267 | ||||||
chr9:98233336
|
C | T | 7 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.781+80G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233336 | ||||||
chr9:98233337
|
G | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.781+79C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233337 | ||||||
chr9:98233367
|
C | T | 5 | a0002c0003t0001g0018a0002c0003t0001g0230a0002c0003t0001g0273others(2): Show | 9 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+49G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 4/12 | chr9 | 98233367 | ||||||
chr9:98233590
|
T | C | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-41A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233590 | ||||||
chr9:98233650
|
A | G | 1 | a0004c0005t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648-101T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233650 | ||||||
chr9:98233717
|
T | C | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.648-168A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233717 | ||||||
chr9:98233736
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(38): Show | 44 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.648-187A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233736 | ||||||
chr9:98233800
|
T | C | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-251A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233800 | ||||||
chr9:98233993
|
T | C | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-444A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98233993 | ||||||
chr9:98234155
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-606C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234155 | ||||||
chr9:98234181
|
T | A | 1 | a0001c0002t0001g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.648-632A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234181 | ||||||
chr9:98234578
|
C | T | 63 | a0003c0004t0001g0005a0003c0004t0001g0045a0003c0004t0001g0057others(60): Show | 65 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.648-1029G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234578 | ||||||
chr9:98234674
|
G | A | 14 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(11): Show | 14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.648-1125C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234674 | ||||||
chr9:98234706
|
G | A | 45 | a0003c0004t0001g0005a0003c0004t0001g0057a0003c0004t0001g0102others(42): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1157C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234706 | ||||||
chr9:98234712
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648-1163G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234712 | ||||||
chr9:98234830
|
C | T | 45 | a0003c0004t0001g0005a0003c0004t0001g0057a0003c0004t0001g0102others(42): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1281G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234830 | ||||||
chr9:98234874
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-1325C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234874 | ||||||
chr9:98234934
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0121 | 2 | HG00741.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.648-1385C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98234934 | ||||||
chr9:98235073
|
G | A | 45 | a0003c0004t0001g0005a0003c0004t0001g0057a0003c0004t0001g0102others(42): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-1524C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235073 | ||||||
chr9:98235125
|
C | T | 6 | a0003c0004t0001g0005a0003c0004t0001g0285a0003c0004t0001g0286others(3): Show | 8 | HG02109.hp2 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.648-1576G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235125 | ||||||
chr9:98235154
|
G | A | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.648-1605C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235154 | ||||||
chr9:98235629
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.648-2080G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235629 | ||||||
chr9:98235734
|
T | A | 6 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0221others(3): Show | 8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.648-2185A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235734 | ||||||
chr9:98235830
|
C | T | 14 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(11): Show | 14 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.648-2281G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235830 | ||||||
chr9:98235844
|
C | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(45): Show | 51 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.648-2295G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235844 | ||||||
chr9:98235848
|
C | T | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.648-2299G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235848 | ||||||
chr9:98235867
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.648-2318A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235867 | ||||||
chr9:98235966
|
T | C | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-2417A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235966 | ||||||
chr9:98235983
|
C | T | 1 | a0003c0012t0001g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.648-2434G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235983 | ||||||
chr9:98235992
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-2443C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98235992 | ||||||
chr9:98236031
|
A | G | 147 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.648-2482T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236031 | ||||||
chr9:98236422
|
C | T | 1 | a0002c0030t0001g0252 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.648-2873G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236422 | ||||||
chr9:98236882
|
G | A | 1 | a0004c0005t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648-3333C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236882 | ||||||
chr9:98236899
|
G | A | 4 | a0002c0003t0001g0282a0002c0003t0001g0327a0017c0027t0001g0275others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-3350C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236899 | ||||||
chr9:98236928
|
AT | A | 85 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(82): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.648-3380delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98236928 | ||||||
chr9:98237000
|
T | C | 2 | a0003c0004t0001g0311a0003c0004t0001g0312 | 2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.648-3451A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237000 | ||||||
chr9:98237036
|
G | C | 45 | a0003c0004t0001g0005a0003c0004t0001g0057a0003c0004t0001g0102others(42): Show | 47 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.648-3487C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237036 | ||||||
chr9:98237042
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.648-3493T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237042 | ||||||
chr9:98237107
|
C | T | 2 | a0003c0036t0001g0288a0006c0035t0001g0295 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.648-3558G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237107 | ||||||
chr9:98237161
|
A | G | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-3612T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237161 | ||||||
chr9:98237166
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.648-3617C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237166 | ||||||
chr9:98237303
|
C | T | 1 | a0004c0005t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.648-3754G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237303 | ||||||
chr9:98237344
|
CA | C | 83 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(80): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.648-3796delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237344 | ||||||
chr9:98237382
|
C | T | 147 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(144): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.648-3833G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237382 | ||||||
chr9:98237545
|
C | T | 1 | a0003c0009t0001g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.648-3996G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237545 | ||||||
chr9:98237546
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.648-3997C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237546 | ||||||
chr9:98237668
|
G | A | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.648-4119C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237668 | ||||||
chr9:98237833
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.648-4284T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237833 | ||||||
chr9:98237860
|
G | A | 1 | a0013c0041t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.648-4311C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237860 | ||||||
chr9:98237870
|
T | C | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.648-4321A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237870 | ||||||
chr9:98237909
|
CT | C | 68 | a0001c0001t0001g0164a0001c0002t0001g0146a0001c0002t0001g0176others(65): Show | 75 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.648-4361delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237909 | ||||||
chr9:98237953
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.648-4404C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98237953 | ||||||
chr9:98238006
|
C | T | 1 | a0001c0002t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.648-4457G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238006 | ||||||
chr9:98238007
|
GATTCTCC others(812): Show |
G | 61 | a0003c0004t0001g0005a0003c0004t0001g0045a0003c0004t0001g0283others(58): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.647+5168_648-4459d others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238007 | ||||||
chr9:98238050
|
T | C | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.648-4501A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238050 | ||||||
chr9:98238226
|
T | C | 84 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(81): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.648-4677A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238226 | ||||||
chr9:98238404
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.648-4855A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238404 | ||||||
chr9:98238729
|
G | GT | 7 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.648-5181dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238729 | ||||||
chr9:98238842
|
C | A | 2 | a0003c0004t0001g0314a0003c0004t0001g0315 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.647+5152G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238842 | ||||||
chr9:98238871
|
T | C | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+5123A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238871 | ||||||
chr9:98238875
|
A | C | 7 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.647+5119T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98238875 | ||||||
chr9:98239224
|
A | T | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+4770T>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239224 | ||||||
chr9:98239335
|
G | T | 2 | a0003c0004t0001g0297a0003c0004t0001g0298 | 2 | HG00408.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.647+4659C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239335 | ||||||
chr9:98239345
|
G | A | 1 | a0002c0003t0001g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647+4649C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239345 | ||||||
chr9:98239761
|
A | ATATT | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+4229_647+4232d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239761 | ||||||
chr9:98239798
|
T | C | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+4196A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239798 | ||||||
chr9:98239865
|
G | T | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+4129C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239865 | ||||||
chr9:98239889
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(47): Show | 53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+4105C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98239889 | ||||||
chr9:98240153
|
G | A | 15 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(12): Show | 18 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.647+3841C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240153 | ||||||
chr9:98240164
|
GTGGT | G | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+3826_647+3829d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240164 | ||||||
chr9:98240166
|
G | GGT | 15 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0002t0001g0132others(12): Show | 15 | HG00140.hp1 HG00735.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.647+3826_647+3827d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
G | GGTGT | 7 | a0002c0014t0001g0025a0002c0014t0001g0026a0003c0004t0003g0046others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+3824_647+3827d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
G | GGTGTGT | 37 | a0002c0030t0001g0252a0003c0004t0001g0005a0003c0004t0001g0283others(34): Show | 39 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.647+3822_647+3827d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
G | GGTGTGTG others(1): Show |
72 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(69): Show | 79 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.647+3820_647+3827d others(10): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
G | GGTGTGTG others(3): Show |
7 | a0002c0003t0001g0229a0002c0003t0001g0254a0002c0003t0001g0255others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+3818_647+3827d others(12): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
G | GGTGTGTG others(5): Show |
2 | a0002c0003t0001g0228a0002c0003t0001g0269 | 2 | NA18945.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.647+3816_647+3827d others(14): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
GGT | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(45): Show | 51 | HG00642.hp2 HG00673.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.647+3826_647+3827d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
GGTGT | G | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+3824_647+3827d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240166
|
GGTGTGT | G | 8 | a0002c0003t0001g0282a0002c0003t0001g0327a0003c0004t0001g0045others(5): Show | 8 | HG01081.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+3822_647+3827d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240166 | ||||||
chr9:98240257
|
G | C | 62 | a0002c0030t0001g0252a0003c0004t0001g0005a0003c0004t0001g0045others(59): Show | 64 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.647+3737C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240257 | ||||||
chr9:98240280
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(47): Show | 53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+3714G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240280 | ||||||
chr9:98240352
|
T | A | 79 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(76): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+3642A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240352 | ||||||
chr9:98240368
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.647+3626C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240368 | ||||||
chr9:98240503
|
T | G | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.647+3491A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240503 | ||||||
chr9:98240586
|
T | C | 15 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(12): Show | 18 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.647+3408A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240586 | ||||||
chr9:98240829
|
C | A | 2 | a0003c0004t0001g0311a0003c0004t0001g0312 | 2 | HG01952.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.647+3165G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98240829 | ||||||
chr9:98241007
|
C | T | 1 | a0001c0002t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.647+2987G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241007 | ||||||
chr9:98241104
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(38): Show | 44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.647+2890A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241104 | ||||||
chr9:98241163
|
C | T | 3 | a0005c0010t0001g0035a0005c0010t0001g0037a0005c0010t0001g0038 | 3 | HG02559.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.647+2831G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241163 | ||||||
chr9:98241168
|
T | C | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.647+2826A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241168 | ||||||
chr9:98241176
|
A | C | 1 | a0012c0040t0001g0147 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.647+2818T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241176 | ||||||
chr9:98241778
|
C | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+2216G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241778 | ||||||
chr9:98241849
|
C | T | 2 | a0003c0011t0001g0029a0003c0034t0001g0047 | 2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.647+2145G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241849 | ||||||
chr9:98241900
|
C | T | 12 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(9): Show | 12 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.647+2094G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241900 | ||||||
chr9:98241904
|
G | C | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+2090C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98241904 | ||||||
chr9:98242179
|
C | T | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+1815G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242179 | ||||||
chr9:98242180
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(47): Show | 53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.647+1814C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242180 | ||||||
chr9:98242206
|
C | T | 2 | a0001c0002t0001g0134a0001c0002t0001g0175 | 2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.647+1788G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242206 | ||||||
chr9:98242269
|
A | G | 145 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(142): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.647+1725T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242269 | ||||||
chr9:98242297
|
C | T | 7 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.647+1697G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242297 | ||||||
chr9:98242370
|
A | G | 328 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.647+1624T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242370 | ||||||
chr9:98242386
|
A | G | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647+1608T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242386 | ||||||
chr9:98242441
|
CA | C | 8 | a0001c0001t0001g0077a0001c0008t0001g0122a0001c0008t0001g0123others(5): Show | 8 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+1552delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242441 | ||||||
chr9:98242525
|
G | C | 6 | a0001c0008t0001g0122a0001c0008t0001g0123a0001c0008t0001g0124others(3): Show | 6 | HG01081.hp2 HG01255.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+1469C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242525 | ||||||
chr9:98242745
|
G | A | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.647+1249C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242745 | ||||||
chr9:98242751
|
C | G | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+1243G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242751 | ||||||
chr9:98242803
|
C | CT | 48 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0064others(45): Show | 50 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.647+1190dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
C | CTT | 12 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0111others(9): Show | 12 | HG00621.hp2 HG00741.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.647+1189_647+1190d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
C | CTTT | 28 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(25): Show | 31 | HG00558.hp2 HG00642.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.647+1188_647+1190d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
C | CTTTT | 35 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.647+1187_647+1190d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
C | CTTTTT | 20 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0287others(17): Show | 22 | HG00280.hp1 HG00408.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.647+1186_647+1190d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
C | CTTTTTTT others(4): Show |
1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+1180_647+1190d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
CTTTT | C | 11 | a0002c0003t0001g0220a0003c0009t0001g0032a0003c0009t0001g0033others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.647+1187_647+1190d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
CTTTTT | C | 6 | a0002c0003t0001g0219a0002c0003t0001g0224a0002c0003t0001g0226others(3): Show | 6 | HG01361.hp1 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.647+1186_647+1190d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
CTTTTTT | C | 60 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(57): Show | 67 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.647+1185_647+1190d others(8): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98242803
|
CTTTTTTT | C | 17 | a0002c0003t0001g0255a0002c0003t0001g0273a0002c0003t0001g0282others(14): Show | 20 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.647+1184_647+1190d others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98242803 | ||||||
chr9:98243008
|
G | A | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.647+986C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243008 | ||||||
chr9:98243069
|
G | C | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+925C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243069 | ||||||
chr9:98243161
|
C | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+833G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243161 | ||||||
chr9:98243210
|
G | C | 12 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(9): Show | 12 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.647+784C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243210 | ||||||
chr9:98243250
|
A | G | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+744T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243250 | ||||||
chr9:98243260
|
C | A | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+734G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243260 | ||||||
chr9:98243263
|
C | G | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+731G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243263 | ||||||
chr9:98243265
|
C | G | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.647+729G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243265 | ||||||
chr9:98243326
|
C | T | 1 | a0004c0005t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.647+668G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243326 | ||||||
chr9:98243353
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.647+641C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243353 | ||||||
chr9:98243354
|
T | C | 1 | a0002c0003t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.647+640A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243354 | ||||||
chr9:98243453
|
C | T | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.647+541G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243453 | ||||||
chr9:98243454
|
G | A | 1 | a0002c0007t0001g0272 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.647+540C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243454 | ||||||
chr9:98243463
|
G | A | 2 | a0002c0003t0001g0254a0002c0003t0001g0255 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.647+531C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243463 | ||||||
chr9:98243534
|
A | AT | 69 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0002g0021others(66): Show | 76 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.647+459dupA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | ||||||
chr9:98243534
|
A | ATT | 16 | a0002c0003t0001g0224a0002c0003t0001g0225a0002c0003t0001g0273others(13): Show | 19 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.647+458_647+459dup others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | ||||||
chr9:98243534
|
AT | A | 50 | a0001c0001t0001g0115a0001c0002t0001g0170a0003c0004t0001g0005others(47): Show | 52 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.647+459delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243534 | ||||||
chr9:98243570
|
CTT | C | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.647+422_647+423del others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243570 | ||||||
chr9:98243571
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.647+423A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243571 | ||||||
chr9:98243613
|
T | C | 1 | a0003c0004t0001g0313 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.647+381A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243613 | ||||||
chr9:98243733
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(38): Show | 44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.647+261G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243733 | ||||||
chr9:98243780
|
G | A | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.647+214C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243780 | ||||||
chr9:98243928
|
T | C | 83 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(80): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.647+66A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243928 | ||||||
chr9:98243934
|
A | G | 144 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(141): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.647+60T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243934 | ||||||
chr9:98243959
|
A | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0208 | 2 | NA18953.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.647+35T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243959 | ||||||
chr9:98243984
|
T | C | 1 | a0001c0006t0001g0014 | 2 | NA18945.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.647+10A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 3/12 | chr9 | 98243984 | ||||||
chr9:98244154
|
C | A | 145 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(142): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-25G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244154 | ||||||
chr9:98244161
|
T | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.512-32A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244161 | ||||||
chr9:98244208
|
C | T | 6 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0221others(3): Show | 8 | NA18947.hp1 NA18968.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-79G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244208 | ||||||
chr9:98244387
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.512-258C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244387 | ||||||
chr9:98244413
|
A | C | 145 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(142): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-284T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244413 | ||||||
chr9:98244573
|
C | T | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-444G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244573 | ||||||
chr9:98244596
|
T | C | 2 | a0001c0006t0001g0013a0001c0006t0001g0171 | 3 | HG01993.hp1 HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.512-467A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244596 | ||||||
chr9:98244600
|
A | G | 1 | a0003c0011t0001g0044 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-471T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244600 | ||||||
chr9:98244613
|
C | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(38): Show | 44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.512-484G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244613 | ||||||
chr9:98244640
|
C | A | 2 | a0001c0019t0001g0172a0001c0019t0001g0173 | 2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.512-511G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244640 | ||||||
chr9:98244659
|
C | CA | 39 | a0001c0001t0001g0054a0001c0001t0001g0071a0001c0001t0001g0073others(36): Show | 42 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.512-531dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | ||||||
chr9:98244659
|
C | CAA | 10 | a0002c0003t0001g0221a0002c0003t0001g0282a0002c0003t0001g0327others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.512-532_512-531dup others(2): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | ||||||
chr9:98244659
|
C | CAAA | 60 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(57): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.512-533_512-531dup others(3): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | ||||||
chr9:98244659
|
C | CAAAA | 13 | a0001c0001t0001g0111a0002c0003t0001g0219a0002c0003t0001g0258others(10): Show | 13 | HG01361.hp1 HG01433.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.512-534_512-531dup others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | ||||||
chr9:98244659
|
CA | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0061others(50): Show | 55 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.512-531delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244659 | ||||||
chr9:98244688
|
G | C | 67 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(64): Show | 74 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.512-559C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244688 | ||||||
chr9:98244695
|
A | G | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-566T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244695 | ||||||
chr9:98244992
|
G | C | 8 | a0004c0005t0001g0078a0004c0005t0001g0079a0004c0005t0001g0276others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.512-863C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98244992 | ||||||
chr9:98245000
|
G | A | 1 | a0001c0002t0001g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.512-871C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245000 | ||||||
chr9:98245390
|
A | G | 2 | a0002c0003t0001g0218a0002c0003t0001g0219 | 2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.512-1261T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245390 | ||||||
chr9:98245488
|
G | A | 62 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(59): Show | 69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.512-1359C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245488 | ||||||
chr9:98245514
|
C | T | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-1385G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245514 | ||||||
chr9:98245517
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(47): Show | 53 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.512-1388T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245517 | ||||||
chr9:98245595
|
G | A | 82 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(79): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.512-1466C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245595 | ||||||
chr9:98245990
|
T | C | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512-1861A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98245990 | ||||||
chr9:98246259
|
C | T | 243 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(240): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.512-2130G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246259 | ||||||
chr9:98246300
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.512-2171C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246300 | ||||||
chr9:98246603
|
A | G | 145 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(142): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.512-2474T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246603 | ||||||
chr9:98246672
|
C | T | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-2543G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246672 | ||||||
chr9:98246769
|
C | T | 143 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.512-2640G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246769 | ||||||
chr9:98246794
|
T | C | 42 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(39): Show | 44 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.512-2665A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246794 | ||||||
chr9:98246814
|
G | A | 6 | a0004c0005t0001g0276a0004c0005t0001g0277a0004c0005t0001g0278others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.512-2685C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246814 | ||||||
chr9:98246990
|
C | T | 2 | a0017c0027t0001g0275a0018c0029t0001g0274 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.512-2861G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98246990 | ||||||
chr9:98247006
|
C | T | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.512-2877G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247006 | ||||||
chr9:98247007
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(38): Show | 44 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.512-2878C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247007 | ||||||
chr9:98247025
|
T | TA | 7 | a0001c0001t0001g0074a0001c0001t0001g0112a0001c0001t0001g0121others(4): Show | 7 | HG01192.hp1 HG02055.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.512-2897dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247025 | ||||||
chr9:98247050
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.512-2921C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247050 | ||||||
chr9:98247144
|
G | A | 62 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(59): Show | 69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.512-3015C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247144 | ||||||
chr9:98247187
|
C | T | 47 | a0003c0004t0001g0005a0003c0004t0001g0045a0003c0004t0001g0283others(44): Show | 49 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.512-3058G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247187 | ||||||
chr9:98247241
|
C | T | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.512-3112G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247241 | ||||||
chr9:98247329
|
CA | C | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 186 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.512-3201delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247329 | ||||||
chr9:98247362
|
C | CA | 79 | a0001c0001t0001g0113a0001c0006t0001g0014a0002c0003t0001g0004others(76): Show | 87 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.512-3234dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247362 | ||||||
chr9:98247536
|
A | G | 80 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(77): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.512-3407T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247536 | ||||||
chr9:98247661
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | NA18980.hp2 NA18992.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.512-3532C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247661 | ||||||
chr9:98247724
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.512-3595C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247724 | ||||||
chr9:98247728
|
C | CA | 21 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | HG00621.hp2 HG00741.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.512-3600dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
C | CAAAAAAA others(3): Show |
4 | a0004c0005t0001g0276a0004c0005t0001g0278a0004c0005t0001g0279others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-3609_512-3600d others(12): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
C | CAAAAAAA others(4): Show |
1 | a0004c0005t0001g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.512-3610_512-3600d others(13): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
CA | C | 59 | a0001c0001t0001g0077a0001c0001t0001g0193a0001c0008t0001g0122others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.512-3600delT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
CAA | C | 5 | a0003c0004t0001g0005a0003c0004t0001g0285a0003c0004t0001g0286others(2): Show | 7 | HG02280.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.512-3601_512-3600d others(4): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
CAAAA | C | 59 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(56): Show | 66 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.512-3603_512-3600d others(6): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98247728
|
CAAAAA | C | 10 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(7): Show | 13 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.512-3604_512-3600d others(7): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98247728 | ||||||
chr9:98248068
|
G | A | 23 | a0003c0004t0001g0297a0003c0004t0001g0298a0003c0004t0001g0299others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.511+3717C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248068 | ||||||
chr9:98248153
|
A | G | 1 | a0004c0005t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.511+3632T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248153 | ||||||
chr9:98248260
|
C | T | 6 | a0004c0005t0001g0276a0004c0005t0001g0277a0004c0005t0001g0278others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+3525G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248260 | ||||||
chr9:98248422
|
G | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0077others(48): Show | 54 | HG00140.hp2 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.511+3363C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248422 | ||||||
chr9:98248462
|
C | T | 2 | a0008c0018t0001g0075a0008c0018t0001g0076 | 2 | HG01071.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.511+3323G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248462 | ||||||
chr9:98248524
|
C | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(37): Show | 43 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.511+3261G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248524 | ||||||
chr9:98248847
|
T | G | 20 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(17): Show | 20 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.511+2938A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248847 | ||||||
chr9:98248868
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.511+2917C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248868 | ||||||
chr9:98248925
|
A | C | 1 | a0003c0004t0001g0283 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.511+2860T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98248925 | ||||||
chr9:98249031
|
C | A | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+2754G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249031 | ||||||
chr9:98249065
|
G | A | 4 | a0003c0004t0001g0320a0003c0004t0001g0321a0003c0004t0001g0322others(1): Show | 4 | HG02809.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+2720C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249065 | ||||||
chr9:98249076
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.511+2709G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249076 | ||||||
chr9:98249270
|
C | T | 44 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(41): Show | 46 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.511+2515G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249270 | ||||||
chr9:98249350
|
C | T | 2 | a0009c0013t0001g0023a0009c0013t0001g0024 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.511+2435G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249350 | ||||||
chr9:98249407
|
C | T | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+2378G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249407 | ||||||
chr9:98249534
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.511+2251G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249534 | ||||||
chr9:98249714
|
T | C | 2 | a0003c0009t0001g0040a0014c0025t0001g0039 | 2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.511+2071A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249714 | ||||||
chr9:98249743
|
T | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0053others(18): Show | 22 | HG00558.hp1 HG01099.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.511+2042A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249743 | ||||||
chr9:98249993
|
G | A | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+1792C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98249993 | ||||||
chr9:98250019
|
AATT | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | HG03942.hp2 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.511+1763_511+1765d others(5): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250019 | ||||||
chr9:98250033
|
C | T | 1 | a0002c0003t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.511+1752G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250033 | ||||||
chr9:98250055
|
G | A | 1 | a0002c0003t0001g0273 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511+1730C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250055 | ||||||
chr9:98250133
|
G | T | 1 | a0016c0021t0001g0022 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.511+1652C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250133 | ||||||
chr9:98250233
|
A | C | 1 | a0003c0004t0001g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.511+1552T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250233 | ||||||
chr9:98250312
|
A | G | 144 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(141): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.511+1473T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250312 | ||||||
chr9:98250326
|
AC | A | 144 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(141): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.511+1458delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250326 | ||||||
chr9:98250402
|
T | A | 1 | a0002c0003t0001g0270 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511+1383A>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250402 | ||||||
chr9:98250474
|
GC | G | 6 | a0004c0005t0001g0276a0004c0005t0001g0277a0004c0005t0001g0278others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.511+1310delG | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250474 | ||||||
chr9:98250542
|
G | A | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+1243C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250542 | ||||||
chr9:98250688
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.511+1097A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250688 | ||||||
chr9:98250825
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.511+960G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250825 | ||||||
chr9:98250865
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.511+920C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250865 | ||||||
chr9:98250896
|
T | G | 62 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(59): Show | 69 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.511+889A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98250896 | ||||||
chr9:98251106
|
G | A | 15 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.511+679C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251106 | ||||||
chr9:98251121
|
C | T | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.511+664G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251121 | ||||||
chr9:98251145
|
C | T | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511+640G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251145 | ||||||
chr9:98251149
|
G | A | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+636C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251149 | ||||||
chr9:98251156
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+629C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251156 | ||||||
chr9:98251157
|
T | C | 74 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(71): Show | 84 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.511+628A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251157 | ||||||
chr9:98251216
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.511+569C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251216 | ||||||
chr9:98251235
|
G | A | 15 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.511+550C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251235 | ||||||
chr9:98251276
|
G | A | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511+509C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251276 | ||||||
chr9:98251290
|
C | CA | 8 | a0002c0014t0001g0025a0002c0014t0001g0026a0003c0004t0001g0045others(5): Show | 8 | HG01081.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.511+494dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251290 | ||||||
chr9:98251366
|
T | G | 1 | a0001c0002t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.511+419A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251366 | ||||||
chr9:98251560
|
C | G | 95 | a0002c0003t0001g0004a0002c0003t0001g0016a0002c0003t0001g0017others(92): Show | 105 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.511+225G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251560 | ||||||
chr9:98251561
|
A | G | 1 | a0001c0002t0001g0055 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.511+224T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 2/12 | chr9 | 98251561 | ||||||
chr9:98252033
|
G | GA | 68 | a0001c0001t0001g0271a0002c0003t0001g0004a0002c0003t0001g0016others(65): Show | 75 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.370-108dupT | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252033 | ||||||
chr9:98252036
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.370-110T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252036 | ||||||
chr9:98252089
|
C | G | 21 | a0003c0004t0001g0045a0003c0004t0003g0046a0003c0009t0001g0032others(18): Show | 21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.370-163G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252089 | ||||||
chr9:98252168
|
T | C | 1 | a0003c0026t0001g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.370-242A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252168 | ||||||
chr9:98252169
|
C | T | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-243G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252169 | ||||||
chr9:98252227
|
A | G | 2 | a0017c0027t0001g0275a0018c0029t0001g0274 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.370-301T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252227 | ||||||
chr9:98252542
|
C | T | 11 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(8): Show | 11 | HG01255.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-616G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252542 | ||||||
chr9:98252678
|
CTAGTCCC others(2): Show |
C | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-761_370-753del others(9): Show |
TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252678 | ||||||
chr9:98252688
|
A | C | 3 | a0002c0003t0001g0273a0002c0007t0001g0002a0002c0007t0001g0272 | 6 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-762T>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252688 | ||||||
chr9:98252770
|
C | A | 5 | a0003c0004t0001g0045a0003c0004t0003g0046a0003c0011t0001g0042others(2): Show | 5 | HG01081.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-844G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252770 | ||||||
chr9:98252777
|
T | C | 7 | a0002c0003t0001g0273a0002c0003t0001g0282a0002c0003t0001g0327others(4): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.370-851A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252777 | ||||||
chr9:98252792
|
G | A | 4 | a0003c0004t0001g0045a0003c0011t0001g0042a0003c0011t0001g0044others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-866C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252792 | ||||||
chr9:98252838
|
G | A | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.370-912C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98252838 | ||||||
chr9:98253151
|
T | C | 15 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.370-1225A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253151 | ||||||
chr9:98253237
|
G | A | 6 | a0004c0005t0001g0276a0004c0005t0001g0277a0004c0005t0001g0278others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1311C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253237 | ||||||
chr9:98253322
|
C | T | 16 | a0003c0009t0001g0032a0003c0009t0001g0033a0003c0009t0001g0036others(13): Show | 16 | HG01243.hp2 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.370-1396G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253322 | ||||||
chr9:98253378
|
A | G | 1 | a0003c0011t0001g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.370-1452T>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253378 | ||||||
chr9:98253467
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.370-1541G>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253467 | ||||||
chr9:98253523
|
G | A | 21 | a0003c0004t0001g0045a0003c0004t0003g0046a0003c0009t0001g0032others(18): Show | 21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.370-1597C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253523 | ||||||
chr9:98253642
|
T | C | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369+1531A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253642 | ||||||
chr9:98253656
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.369+1517G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253656 | ||||||
chr9:98253838
|
G | A | 1 | a0003c0004t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.369+1335C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253838 | ||||||
chr9:98253902
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+1271G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253902 | ||||||
chr9:98253981
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.369+1192C>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98253981 | ||||||
chr9:98254089
|
G | A | 1 | a0003c0034t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369+1084C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254089 | ||||||
chr9:98254170
|
G | C | 2 | a0002c0003t0001g0282a0002c0003t0001g0327 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.369+1003C>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254170 | ||||||
chr9:98254305
|
GT | G | 43 | a0003c0004t0001g0005a0003c0004t0001g0283a0003c0004t0001g0285others(40): Show | 45 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.369+867delA | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254305 | ||||||
chr9:98254416
|
T | G | 2 | a0001c0001t0001g0325a0001c0002t0001g0324 | 2 | HG01515.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.369+757A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254416 | ||||||
chr9:98254554
|
T | C | 2 | a0006c0016t0001g0048a0006c0016t0001g0049 | 2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.369+619A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254554 | ||||||
chr9:98254646
|
T | G | 1 | a0002c0003t0001g0326 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.369+527A>C | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254646 | ||||||
chr9:98254692
|
C | A | 1 | a0002c0003t0001g0327 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+481G>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98254692 | ||||||
chr9:98255017
|
T | C | 1 | a0001c0002t0001g0328 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.369+156A>G | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255017 | ||||||
chr9:98255089
|
C | T | 21 | a0003c0004t0001g0045a0003c0004t0003g0046a0003c0009t0001g0032others(18): Show | 21 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.369+84G>A | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255089 | ||||||
chr9:98255149
|
G | A | 6 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(3): Show | 6 | NA18959.hp2 NA18966.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+24C>T | TBC1D2 | ENSG00000095383.20 | transcript | ENST00000465784.7 | protein_coding | 1/12 | chr9 | 98255149 |