geneid | 9392 |
---|---|
ensemblid | ENSG00000135966.14 |
hgncid | 16836 |
symbol | TGFBRAP1 |
name | transforming growth factor beta receptor associated protein 1 |
refseq_nuc | NM_004257.6 |
refseq_prot | NP_004248.2 |
ensembl_nuc | ENST00000393359.7 |
ensembl_prot | ENSP00000377027.2 |
mane_status | MANE Select |
chr | chr2 |
start | 105264414 |
end | 105329735 |
strand | - |
ver | v1.2 |
region | chr2:105264414-105329735 |
region5000 | chr2:105259414-105334735 |
regionname0 | TGFBRAP1_chr2_105264414_105329735 |
regionname5000 | TGFBRAP1_chr2_105259414_105334735 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 860 | 208 | 51 | 20 | 110 | 6 | 20 | 89 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002 | 0/1 | 860 | 168 | 32 | 44 | 57 | 10 | 24 | 40 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0003 | 0/0 | 860 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0004 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0005 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2583 | 110 | 25 | 12 | 62 | 2 | 9 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0002 | 0/0 | 2583 | 69 | 1 | 13 | 38 | 4 | 13 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0003 | 1/0 | 2583 | 69 | 10 | 6 | 38 | 4 | 10 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0004 | 0/1 | 2583 | 48 | 17 | 13 | 7 | 4 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0005 | 0/0 | 2583 | 24 | 0 | 10 | 8 | 2 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0006 | 0/0 | 2583 | 12 | 8 | 1 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0007 | 0/0 | 2583 | 9 | 6 | 2 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0008 | 0/0 | 2583 | 7 | 0 | 0 | 7 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0009 | 0/0 | 2583 | 7 | 7 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0010 | 0/0 | 2583 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0011 | 0/0 | 2583 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0012 | 0/0 | 2583 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0013 | 0/0 | 2583 | 2 | 0 | 1 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0014 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0015 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0016 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0017 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0018 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0019 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0020 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0021 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0022 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
c0023 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3070 | 114 | 29 | 10 | 65 | 2 | 8 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0002 | 0/0 | 3070 | 63 | 1 | 13 | 33 | 4 | 12 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0003 | 0/0 | 3070 | 31 | 8 | 10 | 9 | 3 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0004 | 1/0 | 3098 | 20 | 0 | 4 | 7 | 2 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0005 | 0/0 | 3070 | 19 | 12 | 2 | 1 | 0 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0006 | 0/1 | 3070 | 18 | 1 | 6 | 7 | 2 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0007 | 0/0 | 3098 | 18 | 8 | 1 | 8 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0008 | 0/0 | 3098 | 11 | 0 | 0 | 11 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0009 | 0/0 | 3098 | 8 | 3 | 1 | 0 | 2 | 2 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0010 | 0/0 | 3070 | 8 | 0 | 6 | 0 | 1 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0011 | 0/0 | 3070 | 7 | 1 | 0 | 6 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0012 | 0/0 | 3071 | 5 | 2 | 0 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0013 | 0/0 | 3070 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0014 | 0/0 | 3070 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0015 | 0/0 | 3070 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0016 | 0/0 | 3070 | 4 | 0 | 2 | 0 | 0 | 2 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0017 | 0/0 | 3070 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0018 | 0/0 | 3071 | 3 | 2 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0019 | 0/0 | 3070 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0020 | 0/0 | 3070 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0021 | 0/0 | 3070 | 2 | 0 | 0 | 1 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0022 | 0/0 | 3070 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0023 | 0/0 | 3070 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0024 | 0/0 | 3098 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0025 | 0/0 | 3071 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0026 | 0/0 | 3098 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0027 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0028 | 0/0 | 3070 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0029 | 0/0 | 3070 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0030 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0031 | 0/0 | 3070 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0032 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0033 | 0/0 | 3070 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0034 | 0/0 | 3098 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0035 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0036 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0037 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0038 | 0/0 | 3070 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0039 | 0/0 | 3098 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0040 | 0/0 | 3098 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0041 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0042 | 0/0 | 3071 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
t0043 | 0/0 | 3099 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2583 | 110 | 25 | 12 | 62 | 2 | 9 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003 | 1/0 | 2583 | 69 | 10 | 6 | 38 | 4 | 10 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006 | 0/0 | 2583 | 12 | 8 | 1 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0008 | 0/0 | 2583 | 7 | 0 | 0 | 7 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0010 | 0/0 | 2583 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0011 | 0/0 | 2583 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0016 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0021 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002 | 0/0 | 2583 | 69 | 1 | 13 | 38 | 4 | 13 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004 | 0/1 | 2583 | 48 | 17 | 13 | 7 | 4 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0005 | 0/0 | 2583 | 24 | 0 | 10 | 8 | 2 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007 | 0/0 | 2583 | 9 | 6 | 2 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0009 | 0/0 | 2583 | 7 | 7 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0012 | 0/0 | 2583 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0013 | 0/0 | 2583 | 2 | 0 | 1 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0017 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0018 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0020 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0022 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0023 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0003c0014 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0004c0019 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0005c0015 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5652 | 95 | 21 | 9 | 56 | 2 | 7 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0005 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0012 | 0/0 | 5653 | 4 | 1 | 0 | 2 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0015 | 0/0 | 5652 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0023 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0024 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0027 | 0/0 | 5638 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0029 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0001t0030 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0004 | 1/0 | 5680 | 19 | 0 | 3 | 7 | 2 | 6 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0007 | 0/0 | 5680 | 18 | 8 | 1 | 8 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0008 | 0/0 | 5680 | 10 | 0 | 0 | 10 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0009 | 0/0 | 5680 | 5 | 0 | 1 | 0 | 2 | 2 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0011 | 0/0 | 5652 | 6 | 0 | 0 | 6 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0020 | 0/0 | 5652 | 3 | 0 | 0 | 3 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0024 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0026 | 0/0 | 5680 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0034 | 0/0 | 5680 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0039 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0040 | 0/0 | 5680 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0041 | 0/0 | 5680 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0003t0043 | 0/0 | 5681 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006t0001 | 0/0 | 5652 | 6 | 4 | 0 | 1 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006t0004 | 0/0 | 5680 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006t0009 | 0/0 | 5680 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006t0012 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0006t0035 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0008t0001 | 0/0 | 5652 | 7 | 0 | 0 | 7 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0010t0001 | 0/0 | 5652 | 4 | 3 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0011t0014 | 0/0 | 5652 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0016t0001 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0001c0021t0008 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002t0002 | 0/0 | 5652 | 63 | 1 | 13 | 33 | 4 | 12 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002t0021 | 0/0 | 5652 | 2 | 0 | 0 | 1 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002t0022 | 0/0 | 5652 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002t0025 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0002t0033 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0003 | 0/0 | 5652 | 11 | 4 | 5 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0005 | 0/0 | 5652 | 10 | 6 | 0 | 0 | 0 | 4 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0006 | 0/1 | 5652 | 18 | 1 | 6 | 7 | 2 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0013 | 0/0 | 5652 | 4 | 4 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0016 | 0/0 | 5652 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0018 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0028 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0031 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0004t0032 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0005t0003 | 0/0 | 5652 | 15 | 0 | 5 | 8 | 1 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0005t0010 | 0/0 | 5652 | 7 | 0 | 5 | 0 | 1 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0005t0036 | 0/0 | 5662 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0005t0042 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007t0003 | 0/0 | 5652 | 3 | 3 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007t0016 | 0/0 | 5652 | 3 | 0 | 2 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007t0019 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007t0037 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0007t0038 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0009t0005 | 0/0 | 5652 | 6 | 6 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0009t0018 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0012t0017 | 0/0 | 5652 | 4 | 0 | 3 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0013t0005 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0013t0018 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0017t0005 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0018t0025 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0020t0003 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0022t0010 | 0/0 | 5652 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0002c0023t0003 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0003c0014t0019 | 0/0 | 5652 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0004c0019t0011 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
a0005c0015t0001 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | copy fasta | chr2 | 105259414 | 105334735 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0012g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0015g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0015g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0023g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0024g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0027g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0029g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0001t0030g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0304 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0008g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0009g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0009g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0011g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0020g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0020g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0024g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0026g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0026g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0034g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0039g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0040g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0041g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0003t0043g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0004g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0009g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0006t0035g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0008t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0010t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0010t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0010t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0011t0014g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0011t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0011t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0016t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0001c0021t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0021g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0021g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0022g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0022g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0025g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0002t0033g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0006g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0016g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0018g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0028g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0031g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0004t0032g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0010g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0036g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0005t0042g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0016g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0016g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0016g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0037g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0007t0038g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0009t0018g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0012t0017g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0012t0017g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0012t0017g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0013t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0013t0018g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0017t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0018t0025g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0020t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0022t0010g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0002c0023t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0003c0014t0019g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0003c0014t0019g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0004c0019t0011g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
a0005c0015t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0002 | g0130 | EUR | GBR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00140 | hp2 | a0001 | c0003 | t0009 | g0126 | EUR | GBR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0174 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00280 | hp2 | a0002 | c0005 | t0003 | g0273 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00323 | hp1 | a0001 | c0003 | t0004 | g0296 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00423 | hp1 | a0002 | c0013 | t0018 | g0253 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00544 | hp2 | a0001 | c0003 | t0007 | g0318 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00558 | hp2 | a0001 | c0008 | t0001 | g0017 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00639 | hp1 | a0002 | c0004 | t0006 | g0206 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00639 | hp2 | a0002 | c0012 | t0017 | g0010 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00642 | hp1 | a0002 | c0022 | t0010 | g0280 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0177 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00673 | hp1 | a0001 | c0006 | t0001 | g0169 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00673 | hp2 | a0002 | c0005 | t0003 | g0277 | EAS | CHS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00735 | hp1 | a0002 | c0005 | t0003 | g0265 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00735 | hp2 | a0002 | c0004 | t0028 | g0220 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00741 | hp1 | a0002 | c0004 | t0006 | g0212 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01070 | hp1 | a0001 | c0001 | t0015 | g0086 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01070 | hp2 | a0002 | c0004 | t0003 | g0354 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01071 | hp1 | a0002 | c0005 | t0003 | g0279 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01071 | hp2 | a0001 | c0001 | t0015 | g0084 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01074 | hp2 | a0002 | c0007 | t0016 | g0345 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01099 | hp2 | a0001 | c0006 | t0004 | g0357 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01106 | hp1 | a0002 | c0005 | t0010 | g0270 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01109 | hp1 | a0002 | c0005 | t0003 | g0264 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01109 | hp2 | a0002 | c0004 | t0003 | g0358 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0162 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01167 | hp2 | a0001 | c0003 | t0007 | g0013 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01175 | hp1 | a0001 | c0003 | t0004 | g0284 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01192 | hp1 | a0002 | c0004 | t0003 | g0356 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01243 | hp1 | a0001 | c0010 | t0001 | g0040 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | PUR | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0149 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01257 | hp2 | a0002 | c0005 | t0010 | g0282 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01258 | hp1 | a0002 | c0005 | t0010 | g0281 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01261 | hp1 | a0002 | c0005 | t0010 | g0261 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01261 | hp2 | a0002 | c0004 | t0006 | g0215 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01346 | hp2 | a0002 | c0004 | t0003 | g0351 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01358 | hp2 | a0001 | c0003 | t0009 | g0023 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01361 | hp1 | a0002 | c0007 | t0016 | g0314 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01361 | hp2 | a0001 | c0003 | t0040 | g0339 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01433 | hp1 | a0002 | c0004 | t0003 | g0355 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0156 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0107 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01515 | hp1 | a0002 | c0005 | t0010 | g0272 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01515 | hp2 | a0002 | c0004 | t0003 | g0015 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01516 | hp2 | a0001 | c0003 | t0009 | g0127 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01517 | hp1 | a0002 | c0004 | t0003 | g0015 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0006 | EUR | IBS | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0153 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01928 | hp2 | a0001 | c0003 | t0004 | g0323 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01934 | hp1 | a0002 | c0004 | t0031 | g0208 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0146 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01952 | hp1 | a0002 | c0004 | t0006 | g0008 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01952 | hp2 | a0002 | c0005 | t0003 | g0276 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01975 | hp1 | a0002 | c0012 | t0017 | g0263 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01975 | hp2 | a0002 | c0004 | t0006 | g0008 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02004 | hp2 | a0002 | c0004 | t0006 | g0218 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02015 | hp1 | a0002 | c0020 | t0003 | g0267 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02015 | hp2 | a0001 | c0003 | t0008 | g0326 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02040 | hp2 | a0001 | c0001 | t0015 | g0052 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02055 | hp1 | a0001 | c0011 | t0014 | g0003 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02055 | hp2 | a0001 | c0006 | t0012 | g0256 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02056 | hp1 | a0001 | c0003 | t0007 | g0334 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02056 | hp2 | a0002 | c0005 | t0003 | g0260 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02080 | hp2 | a0002 | c0005 | t0003 | g0262 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02083 | hp1 | a0002 | c0004 | t0006 | g0211 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02132 | hp1 | a0002 | c0004 | t0006 | g0209 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02148 | hp1 | a0002 | c0005 | t0003 | g0258 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CDX | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02257 | hp1 | a0002 | c0004 | t0003 | g0014 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02257 | hp2 | a0002 | c0007 | t0003 | g0287 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02258 | hp1 | a0002 | c0007 | t0003 | g0344 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02273 | hp1 | a0002 | c0012 | t0017 | g0010 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02273 | hp2 | a0002 | c0017 | t0005 | g0161 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02280 | hp1 | a0002 | c0007 | t0019 | g0292 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02280 | hp2 | a0001 | c0003 | t0007 | g0336 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02300 | hp2 | a0002 | c0013 | t0005 | g0053 | AMR | PEL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02451 | hp1 | a0002 | c0004 | t0005 | g0193 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02451 | hp2 | a0002 | c0009 | t0005 | g0050 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02602 | hp2 | a0001 | c0003 | t0004 | g0289 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02615 | hp1 | a0001 | c0001 | t0030 | g0063 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02622 | hp1 | a0002 | c0004 | t0032 | g0129 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02622 | hp2 | a0002 | c0023 | t0003 | g0359 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02647 | hp1 | a0001 | c0010 | t0001 | g0041 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02683 | hp2 | a0001 | c0003 | t0009 | g0221 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0172 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02698 | hp2 | a0001 | c0003 | t0009 | g0125 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02717 | hp1 | a0004 | c0019 | t0011 | g0353 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02717 | hp2 | a0002 | c0004 | t0013 | g0200 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02723 | hp1 | a0002 | c0004 | t0013 | g0199 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02735 | hp2 | a0001 | c0003 | t0004 | g0290 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02738 | hp1 | a0002 | c0007 | t0016 | g0341 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02738 | hp2 | a0002 | c0005 | t0036 | g0247 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02809 | hp1 | a0001 | c0003 | t0007 | g0346 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02809 | hp2 | a0002 | c0009 | t0018 | g0249 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02818 | hp2 | a0002 | c0004 | t0003 | g0014 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02895 | hp1 | a0001 | c0006 | t0001 | g0202 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02895 | hp2 | a0002 | c0009 | t0005 | g0049 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02897 | hp1 | a0002 | c0009 | t0005 | g0057 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02897 | hp2 | a0002 | c0009 | t0005 | g0051 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02922 | hp1 | a0002 | c0007 | t0003 | g0285 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02922 | hp2 | a0003 | c0014 | t0019 | g0347 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02965 | hp2 | a0002 | c0009 | t0005 | g0048 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02970 | hp2 | a0002 | c0007 | t0038 | g0293 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03017 | hp1 | a0001 | c0003 | t0004 | g0338 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03017 | hp2 | a0001 | c0001 | t0029 | g0241 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03041 | hp1 | a0001 | c0003 | t0041 | g0286 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03041 | hp2 | a0002 | c0004 | t0013 | g0190 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03098 | hp1 | a0002 | c0004 | t0018 | g0257 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0248 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03130 | hp1 | a0001 | c0011 | t0014 | g0035 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03130 | hp2 | a0001 | c0016 | t0001 | g0195 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03139 | hp2 | a0001 | c0011 | t0014 | g0003 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03195 | hp1 | a0001 | c0011 | t0014 | g0036 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03195 | hp2 | a0002 | c0004 | t0013 | g0198 | AFR | ESN | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03209 | hp1 | a0002 | c0004 | t0005 | g0031 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0204 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03239 | hp2 | a0002 | c0004 | t0006 | g0207 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03453 | hp1 | a0001 | c0010 | t0001 | g0060 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03453 | hp2 | a0002 | c0004 | t0005 | g0034 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03486 | hp1 | a0002 | c0004 | t0005 | g0197 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03486 | hp2 | a0001 | c0006 | t0009 | g0033 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03490 | hp2 | a0002 | c0004 | t0005 | g0155 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0160 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03540 | hp1 | a0003 | c0014 | t0019 | g0348 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0203 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0059 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03654 | hp1 | a0001 | c0003 | t0004 | g0288 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03669 | hp2 | a0002 | c0004 | t0005 | g0192 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0142 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03688 | hp2 | a0002 | c0005 | t0042 | g0362 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03704 | hp2 | a0001 | c0003 | t0034 | g0124 | SAS | PJL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0131 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03831 | hp2 | a0001 | c0006 | t0001 | g0148 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03834 | hp2 | a0002 | c0005 | t0010 | g0278 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03942 | hp1 | a0001 | c0003 | t0004 | g0342 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03942 | hp2 | a0002 | c0002 | t0021 | g0188 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04115 | hp1 | a0002 | c0005 | t0003 | g0268 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04115 | hp2 | a0002 | c0004 | t0016 | g0352 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0179 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04184 | hp2 | a0001 | c0003 | t0007 | g0340 | SAS | BEB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04199 | hp1 | a0001 | c0001 | t0012 | g0254 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04199 | hp2 | a0002 | c0004 | t0005 | g0191 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0185 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04228 | hp1 | a0001 | c0003 | t0004 | g0310 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18522 | hp1 | a0001 | c0006 | t0009 | g0002 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18522 | hp2 | a0002 | c0009 | t0005 | g0058 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18612 | hp1 | a0001 | c0003 | t0039 | g0305 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18906 | hp1 | a0002 | c0004 | t0005 | g0196 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18941 | hp2 | a0002 | c0005 | t0003 | g0269 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18943 | hp1 | a0002 | c0004 | t0006 | g0213 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18943 | hp2 | a0002 | c0002 | t0022 | g0184 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18944 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18945 | hp1 | a0001 | c0003 | t0011 | g0315 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18948 | hp1 | a0001 | c0003 | t0008 | g0324 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18948 | hp2 | a0001 | c0006 | t0035 | g0139 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18949 | hp2 | a0001 | c0003 | t0004 | g0295 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18951 | hp1 | a0001 | c0003 | t0020 | g0313 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18952 | hp1 | a0001 | c0003 | t0020 | g0012 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18953 | hp2 | a0001 | c0003 | t0008 | g0299 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18954 | hp2 | a0001 | c0003 | t0007 | g0332 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18961 | hp1 | a0001 | c0003 | t0008 | g0307 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18961 | hp2 | a0001 | c0008 | t0001 | g0019 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18965 | hp2 | a0001 | c0003 | t0008 | g0328 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18968 | hp1 | a0001 | c0003 | t0011 | g0320 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18969 | hp1 | a0002 | c0002 | t0021 | g0175 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18970 | hp2 | a0001 | c0003 | t0004 | g0011 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18973 | hp1 | a0001 | c0003 | t0007 | g0331 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18974 | hp2 | a0001 | c0003 | t0008 | g0308 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18975 | hp2 | a0001 | c0003 | t0011 | g0343 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18977 | hp1 | a0001 | c0008 | t0001 | g0021 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18977 | hp2 | a0001 | c0003 | t0026 | g0361 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18978 | hp1 | a0001 | c0003 | t0007 | g0302 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18978 | hp2 | a0005 | c0015 | t0001 | g0075 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18981 | hp2 | a0001 | c0001 | t0024 | g0114 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18983 | hp1 | a0001 | c0003 | t0008 | g0327 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0251 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18989 | hp2 | a0002 | c0005 | t0003 | g0266 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18990 | hp2 | a0001 | c0003 | t0007 | g0333 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18991 | hp1 | a0001 | c0003 | t0004 | g0319 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18992 | hp1 | a0001 | c0003 | t0011 | g0291 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18993 | hp1 | a0002 | c0002 | t0025 | g0255 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18993 | hp2 | a0001 | c0021 | t0008 | g0297 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18994 | hp1 | a0002 | c0012 | t0017 | g0317 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18995 | hp1 | a0001 | c0003 | t0008 | g0300 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18998 | hp1 | a0002 | c0002 | t0022 | g0183 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19000 | hp2 | a0001 | c0008 | t0001 | g0022 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19002 | hp1 | a0001 | c0003 | t0011 | g0311 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19003 | hp2 | a0001 | c0003 | t0026 | g0360 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19006 | hp2 | a0001 | c0003 | t0007 | g0294 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19011 | hp1 | a0001 | c0003 | t0024 | g0119 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19011 | hp2 | a0001 | c0008 | t0001 | g0018 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19030 | hp1 | a0002 | c0004 | t0006 | g0210 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19030 | hp2 | a0001 | c0003 | t0007 | g0312 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19043 | hp1 | a0001 | c0003 | t0007 | g0337 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19043 | hp2 | a0001 | c0003 | t0007 | g0303 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19056 | hp1 | a0001 | c0003 | t0011 | g0322 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19057 | hp2 | a0002 | c0004 | t0006 | g0205 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19060 | hp2 | a0001 | c0003 | t0004 | g0301 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19062 | hp1 | a0002 | c0005 | t0003 | g0274 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19062 | hp2 | a0001 | c0001 | t0012 | g0252 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19064 | hp2 | a0002 | c0002 | t0033 | g0182 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19065 | hp1 | a0001 | c0003 | t0007 | g0325 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19074 | hp1 | a0002 | c0004 | t0006 | g0216 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19077 | hp1 | a0001 | c0003 | t0008 | g0330 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19078 | hp1 | a0001 | c0001 | t0027 | g0064 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19078 | hp2 | a0002 | c0018 | t0025 | g0250 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19079 | hp1 | a0001 | c0003 | t0020 | g0012 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19080 | hp1 | a0002 | c0004 | t0006 | g0217 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19080 | hp2 | a0001 | c0008 | t0001 | g0020 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19081 | hp2 | a0002 | c0004 | t0006 | g0214 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19082 | hp1 | a0002 | c0005 | t0003 | g0259 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19082 | hp2 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19084 | hp2 | a0001 | c0003 | t0004 | g0306 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19087 | hp2 | a0001 | c0008 | t0001 | g0016 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19091 | hp1 | a0002 | c0005 | t0003 | g0275 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19091 | hp2 | a0001 | c0003 | t0008 | g0329 | EAS | JPT | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19240 | hp1 | a0001 | c0003 | t0007 | g0013 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20129 | hp1 | a0001 | c0001 | t0023 | g0056 | AFR | ASW | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20129 | hp2 | a0001 | c0010 | t0001 | g0061 | AFR | ASW | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20752 | hp2 | a0002 | c0004 | t0006 | g0007 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20805 | hp1 | a0002 | c0004 | t0006 | g0007 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20805 | hp2 | a0001 | c0003 | t0004 | g0298 | EUR | TSI | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20905 | hp1 | a0002 | c0004 | t0005 | g0245 | SAS | GIH | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0171 | SAS | GIH | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01123 | hp1 | a0002 | c0005 | t0010 | g0271 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG01123 | hp2 | a0001 | c0003 | t0004 | g0283 | AMR | CLM | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02109 | hp1 | a0001 | c0006 | t0009 | g0002 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02109 | hp2 | a0002 | c0004 | t0005 | g0194 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02486 | hp1 | a0001 | c0003 | t0043 | g0363 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0222 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG02559 | hp2 | a0001 | c0006 | t0001 | g0201 | AFR | ACB | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG03471 | hp2 | a0002 | c0007 | t0037 | g0321 | AFR | MSL | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
HG06807 | hp2 | a0002 | c0004 | t0003 | g0349 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20300 | hp1 | a0002 | c0004 | t0003 | g0350 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA20300 | hp2 | a0001 | c0003 | t0007 | g0309 | AFR | USA | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
NA21309 | hp2 | a0001 | c0003 | t0007 | g0335 | AFR | LWK | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
homoSapiens_chm13v2 | hp1 | a0002 | c0004 | t0006 | g0219 | REF | REF | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0004 | g0304 | REF | REF | TGFBRAP1_chr2_105259414_105334735 | TGFBRAP1 | chr2 | 105259414 | 105334735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:105269504
|
T | C | 2 | a0002a0003 | 170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
missense_variant | MODERATE | c.2174A>G | p.His725Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2302/5680 | 2174/2583 | 725/860 | chr2 | 105269504 | ||
chr2:105296492
|
G | C | 1 | a0003 | 2 | HG02922.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.902C>G | p.Thr301Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/12 | 1030/5680 | 902/2583 | 301/860 | chr2 | 105296492 | ||
chr2:105307673
|
G | A | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.629C>T | p.Pro210Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 757/5680 | 629/2583 | 210/860 | chr2 | 105307673 | ||
chr2:105308079
|
A | T | 1 | a0005 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.223T>A | p.Phe75Ile | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 351/5680 | 223/2583 | 75/860 | chr2 | 105308079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:105269292
|
A | G | 1 | a0001c0021 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.2386T>C | p.Leu796Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2514/5680 | 2386/2583 | 796/860 | chr2 | 105269292 | ||
chr2:105269416
|
C | T | 1 | a0001c0008 | 7 | HG00558.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2390/5680 | 2262/2583 | 754/860 | chr2 | 105269416 | ||
chr2:105269485
|
G | A | 1 | a0002c0022 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.2193C>T | p.His731His | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/12 | 2321/5680 | 2193/2583 | 731/860 | chr2 | 105269485 | ||
chr2:105272892
|
G | A | 5 | a0002c0005a0002c0013a0002c0017others(2): Show | 29 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(26): Show |
synonymous_variant | LOW | c.1935C>T | p.Leu645Leu | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/12 | 2063/5680 | 1935/2583 | 645/860 | chr2 | 105272892 | ||
chr2:105272937
|
C | T | 1 | a0001c0010 | 4 | HG01243.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.1890G>A | p.Lys630Lys | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/12 | 2018/5680 | 1890/2583 | 630/860 | chr2 | 105272937 | ||
chr2:105280546
|
G | A | 3 | a0002c0002a0002c0012a0002c0018 | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
synonymous_variant | LOW | c.1299C>T | p.Asn433Asn | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/12 | 1427/5680 | 1299/2583 | 433/860 | chr2 | 105280546 | ||
chr2:105298671
|
G | A | 7 | a0001c0001a0001c0008a0001c0010others(4): Show | 132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
synonymous_variant | LOW | c.723C>T | p.Arg241Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/12 | 851/5680 | 723/2583 | 241/860 | chr2 | 105298671 | ||
chr2:105307807
|
C | T | 1 | a0001c0011 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.495G>A | p.Ser165Ser | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 623/5680 | 495/2583 | 165/860 | chr2 | 105307807 | ||
chr2:105307840
|
G | A | 1 | a0001c0011 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 590/5680 | 462/2583 | 154/860 | chr2 | 105307840 | ||
chr2:105307909
|
C | T | 1 | a0002c0020 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.393G>A | p.Gly131Gly | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 521/5680 | 393/2583 | 131/860 | chr2 | 105307909 | ||
chr2:105307966
|
C | T | 1 | a0001c0016 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.336G>A | p.Ser112Ser | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 464/5680 | 336/2583 | 112/860 | chr2 | 105307966 | ||
chr2:105308053
|
A | G | 15 | a0001c0001a0001c0006a0001c0008others(12): Show | 269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
synonymous_variant | LOW | c.249T>C | p.Arg83Arg | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 377/5680 | 249/2583 | 83/860 | chr2 | 105308053 | ||
chr2:105308242
|
G | A | 1 | a0002c0023 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.60C>T | p.Gly20Gly | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/12 | 188/5680 | 60/2583 | 20/860 | chr2 | 105308242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:105264614
|
C | A | 1 | a0001c0001t0023 | 2 | HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2769 | chr2 | 105264614 | |||||
chr2:105264696
|
G | A | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2687C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2687 | chr2 | 105264696 | |||||
chr2:105264914
|
C | A | 1 | a0001c0003t0040 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2469 | chr2 | 105264914 | |||||
chr2:105264915
|
A | G | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2468T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2468 | chr2 | 105264915 | |||||
chr2:105265029
|
A | G | 5 | a0001c0003t0008a0001c0003t0026a0001c0006t0035others(2): Show | 16 | HG02015.hp2 NA18943.hp2 NA18948.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2354T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2354 | chr2 | 105265029 | |||||
chr2:105265090
|
T | C | 5 | a0002c0004t0006a0002c0004t0016a0002c0004t0028others(2): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2293A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2293 | chr2 | 105265090 | |||||
chr2:105265197
|
G | A | 1 | a0001c0001t0029 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2186 | chr2 | 105265197 | |||||
chr2:105265237
|
G | A | 1 | a0001c0003t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2146C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2146 | chr2 | 105265237 | |||||
chr2:105265274
|
T | C | 1 | a0002c0004t0028 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2109 | chr2 | 105265274 | |||||
chr2:105265318
|
AATTAGCT others(7): Show |
A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051_*2064delCACG others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2051 | chr2 | 105265318 | |||||
chr2:105265364
|
G | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2019C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2019 | chr2 | 105265364 | |||||
chr2:105265383
|
C | T | 5 | a0002c0004t0006a0002c0004t0016a0002c0004t0028others(2): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2000G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 2000 | chr2 | 105265383 | |||||
chr2:105265390
|
A | G | 1 | a0001c0011t0014 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1993T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1993 | chr2 | 105265390 | |||||
chr2:105265419
|
A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1964T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1964 | chr2 | 105265419 | |||||
chr2:105265426
|
G | T | 1 | a0002c0002t0021 | 2 | HG03942.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1957 | chr2 | 105265426 | |||||
chr2:105265547
|
G | A | 2 | a0001c0001t0015a0001c0003t0020 | 7 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1836C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1836 | chr2 | 105265547 | |||||
chr2:105265604
|
G | A | 5 | a0002c0002t0002a0002c0002t0025a0002c0002t0033others(2): Show | 70 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1779C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1779 | chr2 | 105265604 | |||||
chr2:105265889
|
A | C | 1 | a0001c0003t0034 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1494 | chr2 | 105265889 | |||||
chr2:105266144
|
C | T | 15 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(12): Show | 137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1239G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1239 | chr2 | 105266144 | |||||
chr2:105266183
|
G | A | 1 | a0001c0006t0035 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1200 | chr2 | 105266183 | |||||
chr2:105266226
|
C | T | 14 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(11): Show | 135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1157 | chr2 | 105266226 | |||||
chr2:105266256
|
A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1127T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1127 | chr2 | 105266256 | |||||
chr2:105266304
|
G | A | 27 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(24): Show | 182 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1079C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1079 | chr2 | 105266304 | |||||
chr2:105266323
|
C | T | 2 | a0002c0005t0010a0002c0022t0010 | 8 | HG00642.hp1 HG01106.hp1 HG01123.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 1060 | chr2 | 105266323 | |||||
chr2:105266411
|
T | C | 1 | a0002c0004t0031 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 972 | chr2 | 105266411 | |||||
chr2:105266479
|
C | T | 4 | a0002c0004t0013a0002c0007t0019a0002c0007t0037others(1): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 904 | chr2 | 105266479 | |||||
chr2:105266484
|
A | G | 1 | a0002c0007t0037 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 899 | chr2 | 105266484 | |||||
chr2:105266536
|
T | C | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 847 | chr2 | 105266536 | |||||
chr2:105266537
|
C | A | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 846 | chr2 | 105266537 | |||||
chr2:105266540
|
A | T | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*843T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 843 | chr2 | 105266540 | |||||
chr2:105266578
|
G | A | 1 | a0002c0004t0032 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 805 | chr2 | 105266578 | |||||
chr2:105266882
|
G | A | 1 | a0002c0007t0038 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 501 | chr2 | 105266882 | |||||
chr2:105266973
|
T | C | 1 | a0001c0003t0041 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 410 | chr2 | 105266973 | |||||
chr2:105267029
|
G | A | 1 | a0002c0002t0033 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 354 | chr2 | 105267029 | |||||
chr2:105267167
|
TTTCCATG others(21): Show |
T | 52 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(49): Show | 313 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*188_*215delTGACCA others(22): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 188 | chr2 | 105267167 | |||||
chr2:105267344
|
A | G | 1 | a0001c0001t0027 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 12/12 | 39 | chr2 | 105267344 | |||||
chr2:105329627
|
G | GCGCCGGC others(3): Show |
1 | a0002c0005t0036 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30_-21dupGGCGCCGG others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21327 | chr2 | 105329627 | |||||
chr2:105329647
|
G | A | 1 | a0001c0003t0026 | 2 | NA18977.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21346 | chr2 | 105329647 | |||||
chr2:105329667
|
G | GC | 9 | a0001c0001t0012a0001c0003t0043a0001c0006t0012others(6): Show | 12 | HG00423.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-61dupG | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21367 | chr2 | 105329667 | |||||
chr2:105329706
|
C | T | 40 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(37): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
5_prime_UTR_variant | MODIFIER | c.-99G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/12 | 21405 | chr2 | 105329706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:105267692
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-133T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267692 | ||||||
chr2:105267802
|
T | C | 29 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0223others(26): Show | 30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.2407-243A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267802 | ||||||
chr2:105267880
|
A | G | 4 | a0001c0003t0011g0315a0001c0003t0011g0320a0001c0003t0011g0322others(1): Show | 4 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2407-321T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267880 | ||||||
chr2:105267934
|
C | G | 2 | a0002c0002t0002g0178a0002c0002t0002g0179 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2407-375G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105267934 | ||||||
chr2:105268043
|
G | A | 30 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2407-484C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268043 | ||||||
chr2:105268109
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2407-550A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268109 | ||||||
chr2:105268262
|
G | A | 3 | a0002c0007t0016g0314a0002c0007t0016g0341a0002c0007t0016g0345 | 3 | HG01074.hp2 HG01361.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2407-703C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268262 | ||||||
chr2:105268331
|
A | C | 1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2407-772T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268331 | ||||||
chr2:105268364
|
G | A | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2407-805C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268364 | ||||||
chr2:105268678
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2406+594C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268678 | ||||||
chr2:105268737
|
A | G | 2 | a0001c0003t0007g0303a0001c0003t0007g0312 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2406+535T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268737 | ||||||
chr2:105268777
|
A | G | 2 | a0001c0008t0001g0017a0001c0008t0001g0018 | 2 | HG00558.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2406+495T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268777 | ||||||
chr2:105268834
|
G | A | 2 | a0001c0003t0011g0320a0001c0003t0011g0322 | 2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2406+438C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268834 | ||||||
chr2:105268852
|
C | A | 135 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2406+420G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268852 | ||||||
chr2:105268875
|
C | A | 13 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350others(10): Show | 14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.2406+397G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268875 | ||||||
chr2:105268896
|
C | T | 1 | a0001c0003t0007g0333 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2406+376G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268896 | ||||||
chr2:105268975
|
C | T | 30 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2406+297G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105268975 | ||||||
chr2:105269007
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2406+265A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269007 | ||||||
chr2:105269048
|
G | A | 6 | a0001c0003t0011g0291a0001c0003t0011g0311a0001c0003t0011g0315others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2406+224C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269048 | ||||||
chr2:105269052
|
A | C | 1 | a0001c0001t0027g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2406+220T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269052 | ||||||
chr2:105269056
|
G | A | 1 | a0001c0001t0027g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2406+216C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269056 | ||||||
chr2:105269114
|
C | A | 2 | a0002c0005t0003g0274a0002c0005t0003g0275 | 2 | NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2406+158G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 11/11 | chr2 | 105269114 | ||||||
chr2:105269739
|
G | A | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1973-34C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269739 | ||||||
chr2:105269756
|
G | A | 1 | a0002c0002t0002g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1973-51C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269756 | ||||||
chr2:105269762
|
C | A | 131 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(128): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1973-57G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269762 | ||||||
chr2:105269926
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-221T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105269926 | ||||||
chr2:105270422
|
C | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-717G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270422 | ||||||
chr2:105270604
|
T | C | 1 | a0001c0006t0004g0357 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1973-899A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270604 | ||||||
chr2:105270699
|
C | G | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1973-994G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105270699 | ||||||
chr2:105271019
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0012g0254 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1973-1314C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271019 | ||||||
chr2:105271092
|
T | C | 92 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(89): Show | 93 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1973-1387A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271092 | ||||||
chr2:105271262
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1973-1557A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271262 | ||||||
chr2:105271549
|
C | G | 1 | a0001c0003t0004g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1972+1306G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271549 | ||||||
chr2:105271768
|
C | T | 1 | a0001c0003t0004g0323 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1972+1087G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271768 | ||||||
chr2:105271835
|
C | T | 18 | a0002c0004t0003g0015a0002c0004t0003g0351a0002c0004t0003g0354others(15): Show | 19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1972+1020G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271835 | ||||||
chr2:105271896
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+959C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271896 | ||||||
chr2:105271922
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0118 | 2 | HG00408.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1972+933C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105271922 | ||||||
chr2:105272037
|
G | A | 1 | a0001c0003t0009g0127 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1972+818C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272037 | ||||||
chr2:105272382
|
C | T | 299 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(296): Show | 313 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.1972+473G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272382 | ||||||
chr2:105272452
|
C | T | 1 | a0001c0010t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1972+403G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272452 | ||||||
chr2:105272626
|
C | T | 1 | a0002c0005t0003g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1972+229G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272626 | ||||||
chr2:105272628
|
T | C | 10 | a0002c0004t0005g0196a0002c0004t0005g0197a0002c0007t0038g0293others(7): Show | 10 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1972+227A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 10/11 | chr2 | 105272628 | ||||||
chr2:105273105
|
C | T | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1813-91G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273105 | ||||||
chr2:105273204
|
A | G | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1813-190T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273204 | ||||||
chr2:105273226
|
C | T | 160 | a0001c0006t0001g0201a0002c0002t0002g0001a0002c0002t0002g0004others(157): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1813-212G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273226 | ||||||
chr2:105273227
|
A | G | 301 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(298): Show | 316 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1813-213T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273227 | ||||||
chr2:105273236
|
G | A | 5 | a0002c0004t0005g0196a0002c0004t0005g0197a0002c0009t0005g0049others(2): Show | 5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-222C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273236 | ||||||
chr2:105273347
|
C | A | 136 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(133): Show | 138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1812+197G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273347 | ||||||
chr2:105273424
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1812+120T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273424 | ||||||
chr2:105273513
|
C | T | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1812+31G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 9/11 | chr2 | 105273513 | ||||||
chr2:105273735
|
C | A | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1666-45G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105273735 | ||||||
chr2:105273949
|
T | G | 1 | a0002c0002t0002g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1666-259A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105273949 | ||||||
chr2:105274011
|
C | T | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1666-321G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274011 | ||||||
chr2:105274121
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1666-431C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274121 | ||||||
chr2:105274163
|
G | A | 2 | a0001c0006t0009g0002a0001c0006t0009g0033 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1666-473C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274163 | ||||||
chr2:105274175
|
T | C | 136 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(133): Show | 138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1666-485A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274175 | ||||||
chr2:105274238
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1666-548C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274238 | ||||||
chr2:105274321
|
C | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1666-631G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274321 | ||||||
chr2:105274476
|
C | T | 1 | a0002c0004t0006g0216 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1666-786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274476 | ||||||
chr2:105274514
|
C | T | 301 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(298): Show | 316 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1666-824G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274514 | ||||||
chr2:105274579
|
C | T | 1 | a0001c0010t0001g0061 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1666-889G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274579 | ||||||
chr2:105274841
|
C | A | 6 | a0001c0003t0009g0023a0001c0003t0009g0125a0001c0003t0009g0126others(3): Show | 6 | HG00140.hp2 HG01358.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+719G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274841 | ||||||
chr2:105274847
|
T | G | 6 | a0001c0003t0011g0291a0001c0003t0011g0311a0001c0003t0011g0315others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+713A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274847 | ||||||
chr2:105274894
|
C | T | 1 | a0001c0001t0023g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1665+666G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274894 | ||||||
chr2:105274945
|
G | A | 1 | a0001c0006t0001g0169 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1665+615C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105274945 | ||||||
chr2:105275004
|
C | A | 2 | a0001c0001t0023g0056a0001c0001t0023g0059 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1665+556G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275004 | ||||||
chr2:105275053
|
C | T | 160 | a0001c0006t0001g0201a0002c0002t0002g0001a0002c0002t0002g0004others(157): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1665+507G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275053 | ||||||
chr2:105275187
|
C | A | 155 | a0001c0006t0001g0201a0002c0002t0002g0001a0002c0002t0002g0004others(152): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1665+373G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275187 | ||||||
chr2:105275221
|
T | A | 3 | a0002c0002t0002g0166a0002c0002t0022g0183a0002c0002t0022g0184 | 3 | HG00544.hp1 NA18943.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1665+339A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275221 | ||||||
chr2:105275257
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1665+303T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275257 | ||||||
chr2:105275274
|
G | T | 1 | a0002c0002t0021g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1665+286C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275274 | ||||||
chr2:105275318
|
G | T | 13 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350others(10): Show | 14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1665+242C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275318 | ||||||
chr2:105275516
|
C | A | 2 | a0002c0007t0019g0292a0002c0007t0037g0321 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1665+44G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 8/11 | chr2 | 105275516 | ||||||
chr2:105275908
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1522-205T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105275908 | ||||||
chr2:105276000
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1522-297A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276000 | ||||||
chr2:105276163
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1522-460A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276163 | ||||||
chr2:105276253
|
T | G | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1522-550A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276253 | ||||||
chr2:105276337
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522-634T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276337 | ||||||
chr2:105276392
|
C | T | 1 | a0002c0022t0010g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1522-689G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276392 | ||||||
chr2:105276399
|
A | G | 360 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(357): Show | 377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.1522-696T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276399 | ||||||
chr2:105276695
|
G | T | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+919C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276695 | ||||||
chr2:105276753
|
C | T | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+861G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276753 | ||||||
chr2:105276810
|
G | A | 128 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(125): Show | 130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1521+804C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276810 | ||||||
chr2:105276990
|
G | A | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1521+624C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105276990 | ||||||
chr2:105277131
|
G | A | 1 | a0001c0008t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1521+483C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277131 | ||||||
chr2:105277162
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0079 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1521+452T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277162 | ||||||
chr2:105277205
|
T | C | 7 | a0001c0003t0004g0011a0001c0003t0004g0295a0001c0003t0004g0306others(4): Show | 8 | NA18612.hp1 NA18944.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1521+409A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277205 | ||||||
chr2:105277350
|
G | GAA | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0001c0011t0014g0003others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+263_1521+264i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277350 | ||||||
chr2:105277400
|
C | G | 5 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(2): Show | 5 | HG02055.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1521+214G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277400 | ||||||
chr2:105277421
|
A | T | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+193T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277421 | ||||||
chr2:105277478
|
C | A | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+136G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 7/11 | chr2 | 105277478 | ||||||
chr2:105277749
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0092 | 2 | NA19002.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1464-78C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277749 | ||||||
chr2:105277770
|
T | C | 13 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350others(10): Show | 14 | HG02257.hp1 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1464-99A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277770 | ||||||
chr2:105277885
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0012g0254 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1464-214A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105277885 | ||||||
chr2:105278068
|
A | ATG | 23 | a0001c0001t0001g0043a0001c0001t0001g0065a0001c0001t0001g0071others(20): Show | 23 | HG00558.hp2 HG01123.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1464-399_1464-398d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATG | A | 46 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(43): Show | 47 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.1464-399_1464-398d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTG | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0225others(15): Show | 19 | HG00408.hp1 HG01099.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1464-401_1464-398d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTG | A | 28 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0072others(25): Show | 29 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1464-403_1464-398d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(1): Show |
A | 41 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036others(38): Show | 43 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1464-405_1464-398d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(3): Show |
A | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1464-407_1464-398d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(5): Show |
A | 11 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(8): Show | 12 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464-409_1464-398d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(7): Show |
A | 24 | a0002c0002t0021g0175a0002c0002t0021g0188a0002c0004t0006g0007others(21): Show | 26 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1464-411_1464-398d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(9): Show |
A | 11 | a0002c0002t0002g0134a0002c0002t0002g0135a0002c0002t0002g0136others(8): Show | 11 | HG02004.hp1 HG02040.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.1464-413_1464-398d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(11): Show |
A | 54 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(51): Show | 61 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1464-415_1464-398d others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278068
|
ATGTGTGT others(15): Show |
A | 1 | a0002c0005t0003g0279 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1464-419_1464-398d others(24): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278068 | ||||||
chr2:105278100
|
G | T | 7 | a0001c0001t0001g0229a0001c0003t0011g0291a0001c0003t0011g0311others(4): Show | 7 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464-429C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278100 | ||||||
chr2:105278103
|
T | C | 8 | a0002c0004t0005g0031a0002c0004t0005g0155a0002c0004t0005g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1464-432A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278103 | ||||||
chr2:105278143
|
G | A | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1464-472C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278143 | ||||||
chr2:105278229
|
G | A | 1 | a0001c0003t0026g0360 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1464-558C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278229 | ||||||
chr2:105278281
|
T | C | 17 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464-610A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278281 | ||||||
chr2:105278305
|
A | G | 1 | a0002c0002t0002g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1464-634T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278305 | ||||||
chr2:105278375
|
A | C | 1 | a0002c0004t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1464-704T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278375 | ||||||
chr2:105278517
|
C | G | 2 | a0002c0004t0005g0196a0002c0004t0005g0197 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1464-846G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278517 | ||||||
chr2:105278537
|
G | T | 65 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(62): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1464-866C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278537 | ||||||
chr2:105278569
|
C | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-898G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278569 | ||||||
chr2:105278656
|
T | C | 2 | a0001c0006t0001g0201a0002c0023t0003g0359 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1464-985A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278656 | ||||||
chr2:105278786
|
T | G | 1 | a0002c0007t0016g0345 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1464-1115A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278786 | ||||||
chr2:105278823
|
G | A | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1464-1152C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278823 | ||||||
chr2:105278850
|
T | C | 2 | a0002c0002t0002g0130a0002c0002t0002g0157 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1464-1179A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105278850 | ||||||
chr2:105279132
|
A | T | 6 | a0002c0004t0005g0196a0002c0004t0005g0197a0002c0007t0038g0293others(3): Show | 6 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463+1250T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279132 | ||||||
chr2:105279227
|
G | A | 1 | a0001c0006t0035g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1463+1155C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279227 | ||||||
chr2:105279228
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1463+1154G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279228 | ||||||
chr2:105279600
|
A | G | 25 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036others(22): Show | 28 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1463+782T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279600 | ||||||
chr2:105279603
|
C | CAAGAAGC others(101): Show |
1 | a0002c0004t0006g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(110): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | ||||||
chr2:105279603
|
C | CAAGAAGC others(118): Show |
14 | a0002c0004t0006g0007a0002c0004t0006g0205a0002c0004t0006g0206others(11): Show | 15 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1463+778_1463+779i others(127): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | ||||||
chr2:105279603
|
C | CAAGAAGC others(119): Show |
5 | a0002c0004t0006g0008a0002c0004t0006g0215a0002c0004t0006g0217others(2): Show | 6 | HG00735.hp2 HG01261.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463+778_1463+779i others(128): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | ||||||
chr2:105279603
|
C | CAAGAAGC others(120): Show |
1 | a0002c0007t0016g0341 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(129): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | ||||||
chr2:105279603
|
C | CAAGAAGC others(121): Show |
1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1463+778_1463+779i others(130): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279603 | ||||||
chr2:105279662
|
C | T | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+720G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279662 | ||||||
chr2:105279679
|
T | A | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+703A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279679 | ||||||
chr2:105279764
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1463+618C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279764 | ||||||
chr2:105279815
|
A | G | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1463+567T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279815 | ||||||
chr2:105279821
|
T | G | 18 | a0001c0006t0001g0201a0002c0004t0003g0015a0002c0004t0003g0351others(15): Show | 19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1463+561A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279821 | ||||||
chr2:105279840
|
C | T | 1 | a0001c0016t0001g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1463+542G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279840 | ||||||
chr2:105279865
|
C | T | 10 | a0002c0005t0003g0279a0002c0005t0010g0261a0002c0005t0010g0270others(7): Show | 10 | HG00642.hp1 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463+517G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279865 | ||||||
chr2:105279907
|
G | A | 163 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(160): Show | 174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1463+475C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279907 | ||||||
chr2:105279924
|
G | GTTAC | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+454_1463+457d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105279924 | ||||||
chr2:105280053
|
TA | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0121a0001c0001t0001g0227others(4): Show | 7 | HG01516.hp2 HG03041.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463+328delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280053 | ||||||
chr2:105280129
|
T | G | 1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1463+253A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280129 | ||||||
chr2:105280236
|
C | A | 17 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(14): Show | 18 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463+146G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280236 | ||||||
chr2:105280264
|
T | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1463+118A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 6/11 | chr2 | 105280264 | ||||||
chr2:105280804
|
C | T | 356 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(353): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1122-81G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105280804 | ||||||
chr2:105280808
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1122-85G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105280808 | ||||||
chr2:105281062
|
C | T | 132 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(129): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1122-339G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281062 | ||||||
chr2:105281101
|
C | T | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1122-378G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281101 | ||||||
chr2:105281185
|
T | C | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1122-462A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281185 | ||||||
chr2:105281283
|
T | G | 300 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(297): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1122-560A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281283 | ||||||
chr2:105281319
|
G | A | 14 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(11): Show | 15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1122-596C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281319 | ||||||
chr2:105281384
|
G | C | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1122-661C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281384 | ||||||
chr2:105281451
|
G | A | 1 | a0002c0004t0006g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1122-728C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281451 | ||||||
chr2:105281453
|
C | T | 2 | a0002c0004t0005g0194a0002c0004t0018g0257 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1122-730G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281453 | ||||||
chr2:105281507
|
T | C | 300 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(297): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1122-784A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281507 | ||||||
chr2:105281664
|
T | G | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-941A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281664 | ||||||
chr2:105281746
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0123 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1122-1023A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281746 | ||||||
chr2:105281780
|
T | G | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1122-1057A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281780 | ||||||
chr2:105281970
|
A | C | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1247T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105281970 | ||||||
chr2:105282176
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1122-1453G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282176 | ||||||
chr2:105282210
|
T | C | 1 | a0002c0020t0003g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1122-1487A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282210 | ||||||
chr2:105282287
|
G | A | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1122-1564C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282287 | ||||||
chr2:105282365
|
T | A | 300 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(297): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1122-1642A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282365 | ||||||
chr2:105282398
|
G | A | 1 | a0002c0002t0002g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1122-1675C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282398 | ||||||
chr2:105282402
|
C | T | 1 | a0002c0002t0002g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1122-1679G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282402 | ||||||
chr2:105282437
|
C | T | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1714G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282437 | ||||||
chr2:105282658
|
C | T | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+1658G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282658 | ||||||
chr2:105282722
|
G | C | 1 | a0001c0003t0007g0340 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+1594C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282722 | ||||||
chr2:105282758
|
C | T | 1 | a0002c0002t0002g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1121+1558G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282758 | ||||||
chr2:105282762
|
G | C | 1 | a0002c0002t0002g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1121+1554C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282762 | ||||||
chr2:105282817
|
T | C | 14 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(11): Show | 15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1121+1499A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282817 | ||||||
chr2:105282831
|
G | A | 1 | a0001c0003t0004g0296 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1121+1485C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | ||||||
chr2:105282831
|
G | GA | 31 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(28): Show | 31 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1121+1484dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | ||||||
chr2:105282831
|
GA | G | 189 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(186): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1121+1484delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282831 | ||||||
chr2:105282854
|
C | T | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+1462G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282854 | ||||||
chr2:105282922
|
G | A | 1 | a0001c0003t0007g0340 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+1394C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282922 | ||||||
chr2:105282944
|
A | G | 1 | a0002c0004t0013g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1121+1372T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105282944 | ||||||
chr2:105283245
|
A | C | 30 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+1071T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283245 | ||||||
chr2:105283267
|
T | C | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1121+1049A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283267 | ||||||
chr2:105283369
|
T | G | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+947A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283369 | ||||||
chr2:105283435
|
T | G | 1 | a0002c0023t0003g0359 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1121+881A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283435 | ||||||
chr2:105283487
|
T | C | 9 | a0002c0004t0003g0015a0002c0004t0003g0351a0002c0004t0003g0354others(6): Show | 10 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1121+829A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283487 | ||||||
chr2:105283504
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1121+812C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283504 | ||||||
chr2:105283564
|
C | T | 1 | a0002c0005t0003g0265 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1121+752G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283564 | ||||||
chr2:105283573
|
A | G | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+743T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283573 | ||||||
chr2:105283677
|
C | T | 1 | a0002c0005t0042g0362 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1121+639G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283677 | ||||||
chr2:105283704
|
G | A | 5 | a0002c0005t0003g0273a0002c0005t0003g0274a0002c0005t0003g0275others(2): Show | 5 | HG00280.hp2 HG00423.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+612C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283704 | ||||||
chr2:105283726
|
G | A | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+590C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283726 | ||||||
chr2:105283809
|
C | T | 1 | a0002c0002t0002g0149 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1121+507G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283809 | ||||||
chr2:105283913
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1121+403A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105283913 | ||||||
chr2:105284094
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1121+222G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105284094 | ||||||
chr2:105284237
|
C | T | 1 | a0002c0004t0005g0196 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1121+79G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 5/11 | chr2 | 105284237 | ||||||
chr2:105284413
|
G | A | 1 | a0001c0003t0007g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1039-15C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284413 | ||||||
chr2:105284430
|
G | GA | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0238others(2): Show | 5 | HG01192.hp2 HG02683.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-33dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284430 | ||||||
chr2:105284433
|
T | A | 4 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-35A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284433 | ||||||
chr2:105284603
|
C | T | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-205G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284603 | ||||||
chr2:105284622
|
C | G | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-224G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284622 | ||||||
chr2:105284650
|
G | A | 60 | a0001c0001t0024g0114a0001c0001t0030g0063a0001c0003t0004g0011others(57): Show | 62 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1039-252C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284650 | ||||||
chr2:105284722
|
G | A | 130 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(127): Show | 132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1039-324C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284722 | ||||||
chr2:105284798
|
A | G | 18 | a0002c0004t0003g0015a0002c0004t0003g0351a0002c0004t0003g0354others(15): Show | 19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-400T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284798 | ||||||
chr2:105284880
|
C | T | 168 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(165): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1039-482G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284880 | ||||||
chr2:105284890
|
A | C | 1 | a0002c0002t0002g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1039-492T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105284890 | ||||||
chr2:105285042
|
A | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1039-644T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285042 | ||||||
chr2:105285096
|
T | C | 191 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(188): Show | 195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1039-698A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285096 | ||||||
chr2:105285183
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1039-785C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285183 | ||||||
chr2:105285216
|
C | T | 79 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0043others(76): Show | 80 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1039-818G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285216 | ||||||
chr2:105285302
|
G | A | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039-904C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285302 | ||||||
chr2:105285315
|
A | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-917T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285315 | ||||||
chr2:105285451
|
A | C | 200 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(197): Show | 206 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1039-1053T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285451 | ||||||
chr2:105285528
|
C | T | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1130G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285528 | ||||||
chr2:105285798
|
T | C | 191 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(188): Show | 195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1039-1400A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285798 | ||||||
chr2:105285957
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-1559T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105285957 | ||||||
chr2:105286016
|
A | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG00741.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-1618T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286016 | ||||||
chr2:105286021
|
A | T | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1623T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286021 | ||||||
chr2:105286074
|
A | G | 9 | a0001c0003t0007g0294a0001c0003t0007g0302a0001c0003t0007g0318others(6): Show | 9 | HG00544.hp2 HG02056.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-1676T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286074 | ||||||
chr2:105286086
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1039-1688C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286086 | ||||||
chr2:105286664
|
T | C | 1 | a0002c0004t0006g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1039-2266A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286664 | ||||||
chr2:105286946
|
T | C | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1039-2548A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105286946 | ||||||
chr2:105287156
|
G | A | 1 | a0001c0003t0004g0323 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-2758C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287156 | ||||||
chr2:105287250
|
G | A | 1 | a0002c0002t0002g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1039-2852C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287250 | ||||||
chr2:105287284
|
A | G | 1 | a0002c0005t0003g0266 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1039-2886T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287284 | ||||||
chr2:105287392
|
AT | A | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-2995delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287392 | ||||||
chr2:105287490
|
C | T | 1 | a0002c0004t0003g0015 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1039-3092G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287490 | ||||||
chr2:105287603
|
A | C | 1 | a0001c0016t0001g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1039-3205T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287603 | ||||||
chr2:105287846
|
T | C | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-3448A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105287846 | ||||||
chr2:105288194
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1039-3796C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288194 | ||||||
chr2:105288205
|
T | C | 300 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(297): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1039-3807A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288205 | ||||||
chr2:105288320
|
G | C | 1 | a0002c0005t0003g0273 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1039-3922C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288320 | ||||||
chr2:105288352
|
G | A | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-3954C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288352 | ||||||
chr2:105288737
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-4339C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288737 | ||||||
chr2:105288742
|
A | G | 6 | a0001c0003t0011g0291a0001c0003t0011g0311a0001c0003t0011g0315others(3): Show | 6 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-4344T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288742 | ||||||
chr2:105288743
|
T | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1039-4345A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288743 | ||||||
chr2:105288797
|
C | T | 132 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(129): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1039-4399G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288797 | ||||||
chr2:105288812
|
T | C | 1 | a0002c0018t0025g0250 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1039-4414A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288812 | ||||||
chr2:105288917
|
C | A | 1 | a0002c0009t0005g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1039-4519G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288917 | ||||||
chr2:105288963
|
A | G | 1 | a0002c0004t0005g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1039-4565T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105288963 | ||||||
chr2:105289208
|
T | TG | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-4811dupC | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289208 | ||||||
chr2:105289292
|
G | A | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-4894C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289292 | ||||||
chr2:105289402
|
G | C | 1 | a0001c0003t0004g0323 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-5004C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289402 | ||||||
chr2:105289411
|
A | C | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5013T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289411 | ||||||
chr2:105289416
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039-5018C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289416 | ||||||
chr2:105289507
|
ATATGT | A | 67 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(64): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1039-5114_1039-511 others(9): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289507 | ||||||
chr2:105289661
|
C | A | 70 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(67): Show | 72 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1039-5263G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289661 | ||||||
chr2:105289810
|
C | A | 22 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(19): Show | 24 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039-5412G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289810 | ||||||
chr2:105289820
|
T | C | 8 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(5): Show | 8 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1039-5422A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289820 | ||||||
chr2:105289904
|
T | A | 1 | a0001c0003t0004g0301 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5506A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289904 | ||||||
chr2:105289905
|
G | A | 1 | a0001c0003t0004g0301 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5507C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289905 | ||||||
chr2:105289953
|
C | G | 30 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(27): Show | 30 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1039-5555G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289953 | ||||||
chr2:105289990
|
G | C | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5592C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105289990 | ||||||
chr2:105290023
|
C | G | 300 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(297): Show | 315 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.1039-5625G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290023 | ||||||
chr2:105290033
|
C | A | 1 | a0001c0003t0004g0301 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1039-5635G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290033 | ||||||
chr2:105290129
|
C | T | 65 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(62): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1039-5731G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290129 | ||||||
chr2:105290258
|
G | A | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-5860C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290258 | ||||||
chr2:105290285
|
T | C | 124 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(121): Show | 126 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1039-5887A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290285 | ||||||
chr2:105290369
|
C | A | 18 | a0002c0004t0003g0015a0002c0004t0003g0351a0002c0004t0003g0354others(15): Show | 19 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5971G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290369 | ||||||
chr2:105290435
|
A | ATGAATTC others(18): Show |
1 | a0002c0002t0002g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1038+5920_1038+592 others(29): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290435 | ||||||
chr2:105290501
|
T | C | 65 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(62): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1038+5855A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290501 | ||||||
chr2:105290551
|
C | T | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+5805G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290551 | ||||||
chr2:105290577
|
GAGAGAGA others(3): Show |
G | 9 | a0001c0003t0008g0324a0001c0003t0008g0326a0001c0003t0008g0327others(6): Show | 9 | HG00544.hp1 HG02015.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+5769_1038+577 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290577 | ||||||
chr2:105290587
|
AAG | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5767_1038+576 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290587 | ||||||
chr2:105290591
|
G | C | 1 | a0002c0007t0038g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1038+5765C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290591 | ||||||
chr2:105290599
|
G | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5757C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290599 | ||||||
chr2:105290605
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5751T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290605 | ||||||
chr2:105290608
|
A | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5748T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290608 | ||||||
chr2:105290610
|
A | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5746T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290610 | ||||||
chr2:105290612
|
A | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5744T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290612 | ||||||
chr2:105290613
|
GAC | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+5741_1038+574 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290613 | ||||||
chr2:105290615
|
C | CTG | 21 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042others(18): Show | 21 | HG00621.hp1 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290615
|
C | CTGTG | 18 | a0001c0001t0001g0039a0001c0001t0001g0077a0001c0001t0001g0079others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290615
|
C | CTGTGTG | 51 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(48): Show | 52 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290615
|
C | CTGTGTGT others(1): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG01243.hp1 HG01496.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290615
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0005g0104a0001c0001t0027g0064 | 2 | HG02523.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1038+5740_1038+574 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290615
|
CAGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1038+5729_1038+574 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290615 | ||||||
chr2:105290616
|
A | AGT | 82 | a0001c0003t0004g0289a0001c0003t0004g0342a0001c0003t0007g0312others(79): Show | 91 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1038+5738_1038+573 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
A | AGTGT | 32 | a0001c0003t0004g0323a0001c0003t0009g0125a0001c0003t0009g0127others(29): Show | 32 | HG00423.hp1 HG01070.hp2 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1038+5736_1038+573 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
A | AGTGTGT | 24 | a0001c0003t0009g0023a0001c0003t0009g0126a0001c0006t0001g0201others(21): Show | 25 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+5734_1038+573 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
A | AGTGTGTG others(1): Show |
13 | a0002c0002t0002g0146a0002c0002t0002g0153a0002c0002t0002g0156others(10): Show | 14 | HG01109.hp2 HG01123.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+5732_1038+573 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
A | AGTGTGTG others(3): Show |
1 | a0002c0004t0003g0355 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1038+5730_1038+573 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
A | T | 128 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(125): Show | 130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1038+5740T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
AGT | A | 10 | a0001c0003t0007g0013a0001c0003t0008g0326a0001c0003t0041g0286others(7): Show | 11 | HG01167.hp2 HG02015.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+5738_1038+573 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
AGTGTGT | A | 5 | a0001c0006t0001g0204a0002c0004t0003g0014a0002c0004t0003g0349others(2): Show | 6 | HG02257.hp1 HG02818.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+5734_1038+573 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0021t0008g0297a0002c0005t0003g0275 | 2 | NA18993.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1038+5728_1038+573 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290616
|
AGTGTGTG others(13): Show |
A | 1 | a0002c0002t0002g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1038+5720_1038+573 others(24): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290616 | ||||||
chr2:105290653
|
G | A | 4 | a0001c0006t0009g0033a0002c0009t0005g0057a0002c0009t0005g0058others(1): Show | 4 | HG02809.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+5703C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290653 | ||||||
chr2:105290653
|
G | GTA | 2 | a0001c0006t0009g0002a0002c0004t0005g0034 | 3 | HG02109.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1038+5702_1038+570 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290653 | ||||||
chr2:105290724
|
G | C | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034others(3): Show | 7 | HG02109.hp1 HG02809.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+5632C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290724 | ||||||
chr2:105290777
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1038+5579C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290777 | ||||||
chr2:105290786
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1038+5570G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290786 | ||||||
chr2:105290796
|
G | C | 132 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(129): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1038+5560C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290796 | ||||||
chr2:105290831
|
C | T | 2 | a0002c0004t0005g0194a0002c0004t0018g0257 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1038+5525G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105290831 | ||||||
chr2:105291071
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0223others(26): Show | 30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.1038+5285G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291071 | ||||||
chr2:105291192
|
T | A | 14 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(11): Show | 14 | HG00673.hp2 HG00735.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038+5164A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291192 | ||||||
chr2:105291257
|
C | T | 1 | a0002c0007t0019g0292 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1038+5099G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291257 | ||||||
chr2:105291333
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1038+5023A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291333 | ||||||
chr2:105291340
|
C | T | 1 | a0002c0004t0006g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1038+5016G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291340 | ||||||
chr2:105291479
|
G | A | 1 | a0001c0010t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1038+4877C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291479 | ||||||
chr2:105291570
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG00741.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291570 | ||||||
chr2:105291604
|
G | A | 29 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0223others(26): Show | 30 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.1038+4752C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291604 | ||||||
chr2:105291651
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1038+4705T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105291651 | ||||||
chr2:105292208
|
A | C | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+4148T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292208 | ||||||
chr2:105292225
|
C | T | 14 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(11): Show | 15 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+4131G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292225 | ||||||
chr2:105292450
|
C | T | 4 | a0002c0004t0005g0031a0002c0004t0005g0193a0002c0004t0005g0194others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+3906G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292450 | ||||||
chr2:105292627
|
C | A | 8 | a0002c0004t0005g0031a0002c0004t0005g0155a0002c0004t0005g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+3729G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292627 | ||||||
chr2:105292716
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1038+3640C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292716 | ||||||
chr2:105292969
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1038+3387C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292969 | ||||||
chr2:105292979
|
G | A | 2 | a0002c0009t0005g0049a0002c0009t0005g0051 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1038+3377C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292979 | ||||||
chr2:105292980
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | NA18984.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1038+3376G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105292980 | ||||||
chr2:105293088
|
T | C | 1 | a0003c0014t0019g0347 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1038+3268A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293088 | ||||||
chr2:105293097
|
A | G | 301 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(298): Show | 316 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1038+3259T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293097 | ||||||
chr2:105293102
|
G | A | 159 | a0001c0003t0041g0286a0001c0006t0001g0202a0001c0006t0001g0203others(156): Show | 170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1038+3254C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293102 | ||||||
chr2:105293550
|
C | T | 1 | a0002c0005t0003g0279 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1038+2806G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293550 | ||||||
chr2:105293737
|
C | T | 25 | a0001c0003t0041g0286a0002c0004t0003g0015a0002c0004t0003g0351others(22): Show | 26 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1038+2619G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293737 | ||||||
chr2:105293746
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1038+2610G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293746 | ||||||
chr2:105293764
|
T | C | 1 | a0001c0006t0004g0357 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1038+2592A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293764 | ||||||
chr2:105293776
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0237 | 2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1038+2580C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293776 | ||||||
chr2:105293915
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1038+2441C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293915 | ||||||
chr2:105293971
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0012g0248a0001c0001t0030g0063 | 3 | HG02559.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1038+2385A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105293971 | ||||||
chr2:105294038
|
T | C | 1 | a0002c0007t0038g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1038+2318A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294038 | ||||||
chr2:105294056
|
G | A | 169 | a0001c0003t0041g0286a0001c0006t0001g0202a0001c0006t0001g0203others(166): Show | 182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1038+2300C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294056 | ||||||
chr2:105294141
|
T | G | 301 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(298): Show | 316 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1038+2215A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294141 | ||||||
chr2:105294205
|
C | T | 2 | a0002c0007t0019g0292a0002c0007t0037g0321 | 2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1038+2151G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294205 | ||||||
chr2:105294270
|
A | C | 1 | a0002c0002t0021g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1038+2086T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294270 | ||||||
chr2:105294307
|
G | GGT | 32 | a0001c0001t0001g0103a0001c0003t0007g0336a0001c0003t0007g0337others(29): Show | 33 | HG00423.hp1 HG01070.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1038+2047_1038+204 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGT | 113 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 116 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1038+2045_1038+204 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGTGT | 36 | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0080others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1038+2043_1038+204 others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGTGTG others(1): Show |
22 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0004t0006g0007others(19): Show | 24 | HG00639.hp1 HG01074.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1038+2041_1038+204 others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGTGTG others(3): Show |
4 | a0001c0003t0020g0012a0001c0003t0020g0313a0002c0004t0006g0207others(1): Show | 5 | HG01109.hp1 HG03239.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+2039_1038+204 others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0012g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1038+2037_1038+204 others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
G | GGTGTGTG others(7): Show |
2 | a0001c0001t0001g0039a0001c0001t0030g0063 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1038+2035_1038+204 others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294307
|
GGTGT | G | 65 | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(62): Show | 72 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1038+2045_1038+204 others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294307 | ||||||
chr2:105294444
|
G | A | 6 | a0002c0004t0013g0190a0002c0004t0013g0198a0002c0004t0013g0199others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+1912C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294444 | ||||||
chr2:105294481
|
A | G | 2 | a0001c0001t0023g0056a0001c0001t0023g0059 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1038+1875T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294481 | ||||||
chr2:105294606
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0102 | 2 | HG00621.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1038+1750C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294606 | ||||||
chr2:105294801
|
C | A | 293 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(290): Show | 308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.1038+1555G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294801 | ||||||
chr2:105294917
|
CT | C | 34 | a0001c0001t0012g0254a0001c0006t0001g0202a0001c0006t0001g0203others(31): Show | 35 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1038+1438delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294917 | ||||||
chr2:105294933
|
C | A | 2 | a0001c0008t0001g0016a0001c0008t0001g0019 | 2 | NA18961.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1038+1423G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294933 | ||||||
chr2:105294939
|
A | G | 155 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(152): Show | 158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1038+1417T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294939 | ||||||
chr2:105294941
|
A | G | 120 | a0001c0001t0012g0254a0001c0006t0001g0148a0001c0006t0001g0202others(117): Show | 129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1038+1415T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294941 | ||||||
chr2:105294976
|
C | T | 1 | a0001c0003t0026g0361 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1038+1380G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294976 | ||||||
chr2:105294978
|
T | C | 3 | a0002c0009t0005g0057a0002c0009t0005g0058a0002c0009t0018g0249 | 3 | HG02809.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1038+1378A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105294978 | ||||||
chr2:105295028
|
C | G | 13 | a0001c0001t0023g0056a0001c0001t0023g0059a0001c0006t0001g0202others(10): Show | 14 | HG02055.hp1 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038+1328G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295028 | ||||||
chr2:105295145
|
A | G | 1 | a0002c0004t0005g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1038+1211T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295145 | ||||||
chr2:105295448
|
G | A | 74 | a0001c0003t0004g0011a0001c0003t0004g0283a0001c0003t0004g0284others(71): Show | 77 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+908C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295448 | ||||||
chr2:105295681
|
G | T | 2 | a0002c0002t0002g0132a0002c0002t0002g0165 | 2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1038+675C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295681 | ||||||
chr2:105295683
|
C | T | 2 | a0002c0002t0002g0132a0002c0002t0002g0165 | 2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1038+673G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295683 | ||||||
chr2:105295714
|
G | A | 26 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(23): Show | 27 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+642C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295714 | ||||||
chr2:105295803
|
C | G | 1 | a0002c0009t0005g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1038+553G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295803 | ||||||
chr2:105295809
|
C | CA | 10 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0082others(7): Show | 10 | HG00621.hp1 HG01109.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1038+546dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | ||||||
chr2:105295809
|
CA | C | 132 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0047others(129): Show | 139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1038+546delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | ||||||
chr2:105295809
|
CAA | C | 20 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(17): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1038+545_1038+546d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295809 | ||||||
chr2:105295868
|
C | G | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1038+488G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295868 | ||||||
chr2:105295905
|
T | C | 68 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0035g0139others(65): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1038+451A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105295905 | ||||||
chr2:105296178
|
G | A | 9 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0048others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1038+178C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105296178 | ||||||
chr2:105296280
|
A | G | 1 | a0002c0004t0005g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1038+76T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 4/11 | chr2 | 105296280 | ||||||
chr2:105296756
|
C | CT | 81 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(78): Show | 84 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.884-247dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | ||||||
chr2:105296756
|
C | CTT | 95 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0223others(92): Show | 102 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.884-248_884-247dup others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | ||||||
chr2:105296756
|
C | CTTT | 32 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0242others(29): Show | 34 | HG00280.hp1 HG00639.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.884-249_884-247dup others(3): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | ||||||
chr2:105296756
|
CT | C | 9 | a0001c0001t0001g0087a0001c0001t0015g0086a0001c0003t0041g0286others(6): Show | 10 | HG01070.hp1 HG01257.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.884-247delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105296756 | ||||||
chr2:105297096
|
G | A | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-586C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297096 | ||||||
chr2:105297308
|
T | A | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.884-798A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297308 | ||||||
chr2:105297442
|
T | G | 2 | a0002c0004t0005g0194a0002c0004t0018g0257 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.884-932A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297442 | ||||||
chr2:105297453
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0079 | 3 | HG01074.hp1 HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.884-943G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297453 | ||||||
chr2:105297573
|
A | G | 119 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(116): Show | 129 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.883+938T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297573 | ||||||
chr2:105297584
|
A | C | 1 | a0001c0003t0007g0013 | 2 | HG01167.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883+927T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297584 | ||||||
chr2:105297913
|
G | A | 1 | a0001c0003t0004g0301 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.883+598C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297913 | ||||||
chr2:105297976
|
A | T | 137 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(134): Show | 140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.883+535T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297976 | ||||||
chr2:105297986
|
C | T | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.883+525G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105297986 | ||||||
chr2:105298016
|
C | G | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+495G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298016 | ||||||
chr2:105298048
|
A | G | 3 | a0002c0009t0005g0049a0002c0009t0005g0050a0002c0009t0005g0051 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.883+463T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298048 | ||||||
chr2:105298050
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+461C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298050 | ||||||
chr2:105298054
|
C | T | 1 | a0002c0004t0005g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.883+457G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298054 | ||||||
chr2:105298058
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.883+453A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298058 | ||||||
chr2:105298217
|
T | C | 1 | a0002c0004t0005g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.883+294A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298217 | ||||||
chr2:105298329
|
C | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+182G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298329 | ||||||
chr2:105298422
|
G | A | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.883+89C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 3/11 | chr2 | 105298422 | ||||||
chr2:105298837
|
G | A | 1 | a0002c0004t0006g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-132C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105298837 | ||||||
chr2:105299040
|
A | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-335T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299040 | ||||||
chr2:105299174
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.689-469C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299174 | ||||||
chr2:105299174
|
G | C | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-469C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299174 | ||||||
chr2:105299254
|
C | T | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-549G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299254 | ||||||
chr2:105299284
|
A | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | NA18949.hp1 NA18968.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.689-579T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299284 | ||||||
chr2:105299368
|
A | G | 1 | a0001c0003t0009g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.689-663T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299368 | ||||||
chr2:105299370
|
G | T | 1 | a0002c0007t0003g0344 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.689-665C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299370 | ||||||
chr2:105299549
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0123others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-844C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299549 | ||||||
chr2:105299631
|
G | A | 1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-926C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299631 | ||||||
chr2:105299636
|
T | C | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-931A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299636 | ||||||
chr2:105299781
|
C | T | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1076G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105299781 | ||||||
chr2:105300178
|
A | T | 284 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(281): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.689-1473T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300178 | ||||||
chr2:105300252
|
G | A | 8 | a0001c0003t0007g0294a0001c0003t0007g0302a0001c0003t0007g0318others(5): Show | 8 | HG00544.hp2 HG02056.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-1547C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300252 | ||||||
chr2:105300406
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0123 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.689-1701G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300406 | ||||||
chr2:105300434
|
C | CT | 71 | a0001c0003t0004g0301a0001c0003t0004g0319a0001c0003t0007g0294others(68): Show | 77 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.689-1730dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300434 | ||||||
chr2:105300452
|
TTTC | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-1750_689-1748d others(5): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300452 | ||||||
chr2:105300454
|
TC | T | 128 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(125): Show | 129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.689-1750delG | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300454 | ||||||
chr2:105300454
|
TCC | T | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0073others(9): Show | 12 | HG02083.hp2 HG02148.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.689-1751_689-1750d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300454 | ||||||
chr2:105300455
|
C | T | 100 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0202others(97): Show | 110 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.689-1750G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300455 | ||||||
chr2:105300456
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.689-1751G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300456 | ||||||
chr2:105300597
|
T | G | 1 | a0002c0005t0036g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.689-1892A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300597 | ||||||
chr2:105300640
|
T | C | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.689-1935A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105300640 | ||||||
chr2:105301052
|
G | A | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-2347C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301052 | ||||||
chr2:105301084
|
C | G | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2379G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301084 | ||||||
chr2:105301145
|
C | T | 5 | a0001c0006t0001g0201a0002c0004t0013g0190a0002c0004t0013g0198others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-2440G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301145 | ||||||
chr2:105301154
|
G | A | 1 | a0002c0009t0005g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.689-2449C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301154 | ||||||
chr2:105301226
|
A | G | 16 | a0001c0006t0001g0201a0001c0016t0001g0195a0002c0004t0005g0031others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-2521T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301226 | ||||||
chr2:105301444
|
A | C | 1 | a0002c0004t0018g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.689-2739T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301444 | ||||||
chr2:105301512
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.689-2807C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301512 | ||||||
chr2:105301584
|
CA | C | 4 | a0001c0003t0007g0336a0002c0007t0019g0292a0002c0007t0037g0321others(1): Show | 4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2880delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301584 | ||||||
chr2:105301586
|
A | T | 4 | a0001c0003t0007g0336a0002c0007t0019g0292a0002c0007t0037g0321others(1): Show | 4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2881T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301586 | ||||||
chr2:105301587
|
A | C | 4 | a0001c0003t0007g0336a0002c0007t0019g0292a0002c0007t0037g0321others(1): Show | 4 | HG02280.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2882T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301587 | ||||||
chr2:105301609
|
G | A | 256 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(253): Show | 269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.689-2904C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301609 | ||||||
chr2:105301653
|
A | T | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-2948T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301653 | ||||||
chr2:105301672
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-2967A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301672 | ||||||
chr2:105301881
|
C | T | 1 | a0002c0002t0021g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.689-3176G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301881 | ||||||
chr2:105301890
|
C | G | 1 | a0001c0003t0009g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.689-3185G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301890 | ||||||
chr2:105301897
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.689-3192A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301897 | ||||||
chr2:105301999
|
T | C | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-3294A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105301999 | ||||||
chr2:105302009
|
T | TA | 27 | a0001c0003t0004g0284a0001c0003t0004g0319a0001c0003t0007g0302others(24): Show | 29 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.689-3305dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | ||||||
chr2:105302009
|
T | TAA | 18 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(15): Show | 18 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.689-3306_689-3305d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | ||||||
chr2:105302009
|
TA | T | 154 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(151): Show | 158 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.689-3305delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | ||||||
chr2:105302009
|
TAA | T | 8 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0103others(5): Show | 8 | HG02451.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.689-3306_689-3305d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302009 | ||||||
chr2:105302140
|
A | G | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-3435T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302140 | ||||||
chr2:105302158
|
A | G | 2 | a0001c0003t0007g0303a0001c0003t0007g0312 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.689-3453T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302158 | ||||||
chr2:105302237
|
A | G | 1 | a0004c0019t0011g0353 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.689-3532T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302237 | ||||||
chr2:105302394
|
A | C | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-3689T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302394 | ||||||
chr2:105302437
|
T | C | 1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-3732A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302437 | ||||||
chr2:105302473
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.689-3768A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302473 | ||||||
chr2:105302482
|
A | G | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.689-3777T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302482 | ||||||
chr2:105302487
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.689-3782T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302487 | ||||||
chr2:105302538
|
TA | T | 253 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(250): Show | 266 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.689-3834delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302538 | ||||||
chr2:105302650
|
A | T | 131 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(128): Show | 132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.689-3945T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302650 | ||||||
chr2:105302675
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.689-3970A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302675 | ||||||
chr2:105302686
|
C | T | 1 | a0002c0002t0002g0172 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.689-3981G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302686 | ||||||
chr2:105302886
|
A | T | 20 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.689-4181T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105302886 | ||||||
chr2:105303081
|
G | A | 1 | a0003c0014t0019g0348 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.689-4376C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303081 | ||||||
chr2:105303149
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.689-4444G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303149 | ||||||
chr2:105303259
|
G | A | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.688+4355C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303259 | ||||||
chr2:105303295
|
C | A | 1 | a0002c0005t0003g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.688+4319G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303295 | ||||||
chr2:105303357
|
C | T | 1 | a0002c0002t0002g0176 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.688+4257G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303357 | ||||||
chr2:105303431
|
G | A | 3 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350 | 4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+4183C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303431 | ||||||
chr2:105303433
|
G | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.688+4181C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303433 | ||||||
chr2:105303615
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3999T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303615 | ||||||
chr2:105303628
|
T | G | 9 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0048others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+3986A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303628 | ||||||
chr2:105303710
|
C | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+3904G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303710 | ||||||
chr2:105303754
|
C | G | 1 | a0001c0006t0001g0202 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.688+3860G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303754 | ||||||
chr2:105303754
|
C | T | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.688+3860G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303754 | ||||||
chr2:105303828
|
C | T | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3786G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303828 | ||||||
chr2:105303837
|
C | T | 1 | a0001c0006t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.688+3777G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303837 | ||||||
chr2:105303894
|
C | T | 3 | a0001c0016t0001g0195a0002c0004t0005g0196a0002c0004t0005g0197 | 3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.688+3720G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105303894 | ||||||
chr2:105304026
|
CTAAAAA | C | 4 | a0002c0009t0005g0048a0002c0009t0005g0049a0002c0009t0005g0050others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3582_688+3587d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304026 | ||||||
chr2:105304197
|
T | C | 1 | a0001c0003t0008g0300 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.688+3417A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304197 | ||||||
chr2:105304363
|
A | G | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+3251T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304363 | ||||||
chr2:105304399
|
C | T | 2 | a0002c0002t0002g0164a0002c0002t0002g0246 | 2 | HG02040.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.688+3215G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304399 | ||||||
chr2:105304500
|
C | T | 331 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(328): Show | 347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.688+3114G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304500 | ||||||
chr2:105304507
|
G | A | 2 | a0001c0001t0023g0056a0001c0001t0023g0059 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.688+3107C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304507 | ||||||
chr2:105304554
|
G | A | 1 | a0002c0007t0016g0345 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.688+3060C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304554 | ||||||
chr2:105304762
|
G | A | 1 | a0001c0008t0001g0018 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.688+2852C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304762 | ||||||
chr2:105304764
|
C | T | 1 | a0002c0004t0005g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.688+2850G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304764 | ||||||
chr2:105304783
|
G | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+2831C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105304783 | ||||||
chr2:105305018
|
T | C | 1 | a0002c0020t0003g0267 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.688+2596A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305018 | ||||||
chr2:105305118
|
C | T | 5 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0057others(2): Show | 5 | HG02809.hp2 HG02897.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+2496G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305118 | ||||||
chr2:105305322
|
C | T | 6 | a0001c0003t0007g0294a0001c0003t0007g0302a0001c0003t0007g0331others(3): Show | 6 | HG02056.hp1 NA18954.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+2292G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305322 | ||||||
chr2:105305440
|
G | C | 1 | a0002c0002t0002g0163 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.688+2174C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305440 | ||||||
chr2:105305514
|
A | G | 2 | a0002c0009t0005g0057a0002c0009t0018g0249 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.688+2100T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305514 | ||||||
chr2:105305728
|
G | A | 131 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(128): Show | 132 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.688+1886C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305728 | ||||||
chr2:105305750
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.688+1864G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105305750 | ||||||
chr2:105306057
|
TTTTG | T | 15 | a0001c0006t0001g0201a0001c0016t0001g0195a0002c0004t0005g0031others(12): Show | 15 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1553_688+1556d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306057 | ||||||
chr2:105306061
|
G | GT | 4 | a0001c0001t0012g0251a0001c0006t0009g0002a0002c0004t0003g0354others(1): Show | 5 | HG01070.hp2 HG02109.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+1552dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306061 | ||||||
chr2:105306066
|
T | G | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+1548A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306066 | ||||||
chr2:105306067
|
TG | T | 98 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(95): Show | 98 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.688+1546delC | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306067 | ||||||
chr2:105306068
|
G | T | 158 | a0001c0001t0001g0043a0001c0001t0001g0068a0001c0001t0001g0069others(155): Show | 169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.688+1546C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306068 | ||||||
chr2:105306068
|
GT | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0226others(17): Show | 21 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+1545delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306068 | ||||||
chr2:105306069
|
T | TTG | 90 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0202others(87): Show | 98 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.688+1544_688+1545i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306069 | ||||||
chr2:105306071
|
T | G | 1 | a0002c0012t0017g0263 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.688+1543A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306071 | ||||||
chr2:105306075
|
T | G | 4 | a0001c0003t0011g0315a0001c0003t0011g0320a0001c0003t0011g0322others(1): Show | 4 | NA18945.hp1 NA18968.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+1539A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306075 | ||||||
chr2:105306329
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1285A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306329 | ||||||
chr2:105306335
|
T | G | 1 | a0005c0015t0001g0075 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.688+1279A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306335 | ||||||
chr2:105306336
|
A | T | 1 | a0005c0015t0001g0075 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.688+1278T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306336 | ||||||
chr2:105306341
|
C | T | 137 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(134): Show | 140 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.688+1273G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306341 | ||||||
chr2:105306368
|
T | C | 1 | a0001c0003t0009g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.688+1246A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306368 | ||||||
chr2:105306417
|
G | A | 1 | a0001c0003t0008g0327 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.688+1197C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306417 | ||||||
chr2:105306422
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+1192A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306422 | ||||||
chr2:105306545
|
C | T | 1 | a0002c0002t0002g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.688+1069G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306545 | ||||||
chr2:105306623
|
C | T | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.688+991G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306623 | ||||||
chr2:105306682
|
C | T | 1 | a0002c0005t0003g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.688+932G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306682 | ||||||
chr2:105306702
|
G | T | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+912C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306702 | ||||||
chr2:105306714
|
G | A | 1 | a0001c0003t0026g0360 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.688+900C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306714 | ||||||
chr2:105306791
|
T | C | 3 | a0001c0016t0001g0195a0002c0004t0005g0196a0002c0004t0005g0197 | 3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.688+823A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306791 | ||||||
chr2:105306799
|
A | G | 1 | a0002c0005t0003g0276 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.688+815T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306799 | ||||||
chr2:105306875
|
A | G | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+739T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306875 | ||||||
chr2:105306877
|
A | G | 1 | a0002c0002t0002g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.688+737T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306877 | ||||||
chr2:105306914
|
T | C | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.688+700A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105306914 | ||||||
chr2:105307188
|
ACT | A | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+424_688+425del others(2): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307188 | ||||||
chr2:105307514
|
G | A | 1 | a0002c0004t0006g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.688+100C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307514 | ||||||
chr2:105307534
|
G | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.688+80C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307534 | ||||||
chr2:105307560
|
C | T | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.688+54G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307560 | ||||||
chr2:105307570
|
G | A | 16 | a0001c0006t0001g0201a0001c0016t0001g0195a0002c0004t0005g0031others(13): Show | 16 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.688+44C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 2/11 | chr2 | 105307570 | ||||||
chr2:105308490
|
C | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-172G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308490 | ||||||
chr2:105308624
|
T | C | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-17-306A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308624 | ||||||
chr2:105308701
|
C | T | 3 | a0002c0009t0005g0057a0002c0009t0005g0058a0002c0009t0018g0249 | 3 | HG02809.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-17-383G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308701 | ||||||
chr2:105308708
|
A | G | 38 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(35): Show | 40 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-17-390T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308708 | ||||||
chr2:105308758
|
C | T | 1 | a0002c0002t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17-440G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308758 | ||||||
chr2:105308763
|
TA | T | 136 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(133): Show | 139 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-17-446delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308763 | ||||||
chr2:105308854
|
T | C | 68 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0035g0139others(65): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-536A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105308854 | ||||||
chr2:105309015
|
G | A | 1 | a0002c0002t0021g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-697C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309015 | ||||||
chr2:105309070
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-752G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309070 | ||||||
chr2:105309113
|
G | A | 1 | a0001c0001t0012g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-795C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309113 | ||||||
chr2:105309785
|
C | G | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-1467G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105309785 | ||||||
chr2:105310118
|
T | G | 1 | a0002c0004t0005g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-17-1800A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310118 | ||||||
chr2:105310183
|
G | A | 9 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0048others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-1865C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310183 | ||||||
chr2:105310417
|
T | C | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-17-2099A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310417 | ||||||
chr2:105310484
|
C | T | 1 | a0002c0004t0006g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-17-2166G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310484 | ||||||
chr2:105310569
|
T | C | 1 | a0001c0003t0004g0296 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-2251A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310569 | ||||||
chr2:105310706
|
A | G | 4 | a0002c0005t0003g0258a0002c0005t0042g0362a0002c0012t0017g0010others(1): Show | 5 | HG00639.hp2 HG01975.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-2388T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310706 | ||||||
chr2:105310734
|
T | C | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2416A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310734 | ||||||
chr2:105310842
|
T | C | 1 | a0002c0002t0002g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-17-2524A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310842 | ||||||
chr2:105310854
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-2536A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310854 | ||||||
chr2:105310942
|
A | G | 1 | a0001c0006t0035g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-17-2624T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310942 | ||||||
chr2:105310943
|
C | T | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-2625G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310943 | ||||||
chr2:105310960
|
C | T | 78 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0043others(75): Show | 78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-2642G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105310960 | ||||||
chr2:105311145
|
T | TA | 11 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0003t0007g0312others(8): Show | 13 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-2828dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311145 | ||||||
chr2:105311154
|
A | C | 68 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0035g0139others(65): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-2836T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311154 | ||||||
chr2:105311155
|
A | C | 108 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(105): Show | 116 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-17-2837T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311155 | ||||||
chr2:105311161
|
A | AAC | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-2844_-17-2843i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311161 | ||||||
chr2:105311162
|
C | A | 31 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350others(28): Show | 33 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-2844G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311162 | ||||||
chr2:105311169
|
C | A | 3 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350 | 4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2851G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311169 | ||||||
chr2:105311253
|
GT | G | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-17-2936delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311253 | ||||||
chr2:105311348
|
G | A | 20 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-3030C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311348 | ||||||
chr2:105311539
|
T | C | 284 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(281): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.-17-3221A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311539 | ||||||
chr2:105311588
|
G | GA | 5 | a0001c0006t0001g0201a0002c0004t0013g0190a0002c0004t0013g0198others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-3271dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311588 | ||||||
chr2:105311648
|
C | T | 1 | a0002c0002t0002g0153 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-3330G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311648 | ||||||
chr2:105311674
|
G | A | 1 | a0001c0006t0001g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-3356C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311674 | ||||||
chr2:105311750
|
C | A | 9 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0048others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-3432G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105311750 | ||||||
chr2:105312089
|
G | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-3771C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312089 | ||||||
chr2:105312098
|
C | A | 1 | a0002c0013t0005g0053 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-17-3780G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312098 | ||||||
chr2:105312204
|
A | G | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-3886T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312204 | ||||||
chr2:105312303
|
A | T | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-3985T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312303 | ||||||
chr2:105312447
|
A | T | 2 | a0001c0003t0009g0023a0001c0003t0009g0127 | 2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-17-4129T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312447 | ||||||
chr2:105312467
|
C | G | 9 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(6): Show | 10 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-4149G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312467 | ||||||
chr2:105312554
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0223a0001c0001t0001g0224others(20): Show | 24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17-4236C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312554 | ||||||
chr2:105312590
|
G | A | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-4272C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312590 | ||||||
chr2:105312591
|
T | G | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-4273A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312591 | ||||||
chr2:105312867
|
T | C | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-4549A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312867 | ||||||
chr2:105312940
|
T | C | 284 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(281): Show | 298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.-17-4622A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312940 | ||||||
chr2:105312942
|
C | T | 256 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(253): Show | 269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-17-4624G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105312942 | ||||||
chr2:105313069
|
G | A | 1 | a0001c0003t0009g0127 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-17-4751C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313069 | ||||||
chr2:105313125
|
G | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-4807C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313125 | ||||||
chr2:105313257
|
A | C | 1 | a0001c0001t0001g0009 | 2 | NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-17-4939T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313257 | ||||||
chr2:105313444
|
T | C | 287 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(284): Show | 301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.-17-5126A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313444 | ||||||
chr2:105313556
|
T | C | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-5238A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313556 | ||||||
chr2:105313613
|
A | G | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-5295T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313613 | ||||||
chr2:105313687
|
A | G | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-5369T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313687 | ||||||
chr2:105313908
|
C | G | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-17-5590G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313908 | ||||||
chr2:105313949
|
C | A | 1 | a0002c0009t0005g0058 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17-5631G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105313949 | ||||||
chr2:105314082
|
G | C | 9 | a0001c0001t0023g0056a0001c0001t0023g0059a0002c0009t0005g0048others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-5764C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314082 | ||||||
chr2:105314249
|
C | CT | 19 | a0001c0001t0001g0076a0001c0003t0004g0301a0001c0003t0007g0336others(16): Show | 19 | HG01175.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-5932dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | ||||||
chr2:105314249
|
C | CTT | 14 | a0001c0006t0001g0201a0002c0004t0005g0191a0002c0004t0005g0192others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-5933_-17-5932d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | ||||||
chr2:105314249
|
CT | C | 126 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(123): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-17-5932delA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314249 | ||||||
chr2:105314264
|
T | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-5946A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314264 | ||||||
chr2:105314278
|
T | A | 1 | a0002c0005t0003g0279 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-17-5960A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314278 | ||||||
chr2:105314282
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0223a0001c0001t0001g0224others(20): Show | 24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17-5964C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314282 | ||||||
chr2:105314283
|
C | G | 1 | a0002c0004t0006g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-5965G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314283 | ||||||
chr2:105314310
|
T | G | 256 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(253): Show | 269 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-17-5992A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314310 | ||||||
chr2:105314352
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-17-6034C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314352 | ||||||
chr2:105314529
|
C | T | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-6211G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314529 | ||||||
chr2:105314531
|
T | C | 3 | a0001c0016t0001g0195a0002c0004t0005g0196a0002c0004t0005g0197 | 3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-17-6213A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314531 | ||||||
chr2:105314628
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-17-6310C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314628 | ||||||
chr2:105314708
|
G | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6390C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314708 | ||||||
chr2:105314860
|
G | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6542C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314860 | ||||||
chr2:105314949
|
C | CA | 53 | a0001c0001t0001g0091a0001c0001t0001g0122a0001c0001t0024g0114others(50): Show | 58 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-17-6632dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314949 | ||||||
chr2:105314949
|
CA | C | 22 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0006t0001g0201others(19): Show | 22 | HG01169.hp2 HG02109.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-6632delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105314949 | ||||||
chr2:105315018
|
ACT | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-6702_-17-6701d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315018 | ||||||
chr2:105315057
|
A | C | 1 | a0002c0002t0002g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-17-6739T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315057 | ||||||
chr2:105315236
|
G | A | 9 | a0001c0003t0008g0299a0001c0003t0008g0300a0001c0003t0008g0307others(6): Show | 10 | NA18951.hp1 NA18952.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-6918C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315236 | ||||||
chr2:105315418
|
A | G | 1 | a0001c0003t0011g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-17-7100T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315418 | ||||||
chr2:105315609
|
C | T | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-7291G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315609 | ||||||
chr2:105315881
|
G | T | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-7563C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315881 | ||||||
chr2:105315905
|
C | T | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-17-7587G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315905 | ||||||
chr2:105315923
|
A | G | 1 | a0005c0015t0001g0075 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-17-7605T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105315923 | ||||||
chr2:105316287
|
G | C | 1 | a0002c0005t0003g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-17-7969C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316287 | ||||||
chr2:105316340
|
CA | C | 16 | a0001c0001t0001g0244a0001c0003t0011g0291a0001c0006t0004g0357others(13): Show | 18 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-8023delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316340 | ||||||
chr2:105316341
|
A | C | 1 | a0002c0002t0002g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-17-8023T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316341 | ||||||
chr2:105316420
|
A | AGT | 34 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0054others(31): Show | 36 | HG00408.hp2 HG01074.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-17-8104_-17-8103d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
A | AGTGT | 15 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 15 | HG00558.hp2 HG00621.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8106_-17-8103d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
A | AGTGTGT | 8 | a0001c0001t0001g0043a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 8 | HG02300.hp1 HG03704.hp1 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-8108_-17-8103d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0090others(4): Show | 7 | HG00323.hp1 HG02165.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-8110_-17-8103d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-17-8114_-17-8103d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
AGT | A | 6 | a0001c0001t0001g0115a0001c0001t0023g0059a0001c0003t0004g0338others(3): Show | 7 | HG00741.hp2 HG01167.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-8104_-17-8103d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316420
|
AGTGT | A | 5 | a0001c0001t0001g0055a0001c0003t0004g0323a0001c0003t0004g0342others(2): Show | 5 | HG01928.hp2 HG03942.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-8106_-17-8103d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316420 | ||||||
chr2:105316422
|
T | A | 2 | a0002c0004t0005g0194a0002c0004t0018g0257 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-17-8104A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316422 | ||||||
chr2:105316446
|
TGTGTGTG others(19): Show |
T | 2 | a0002c0009t0005g0049a0002c0009t0005g0051 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-8154_-17-8129d others(28): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316446 | ||||||
chr2:105316452
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17-8148_-17-8135d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316452 | ||||||
chr2:105316454
|
TGTGTGTG others(7): Show |
T | 1 | a0002c0002t0002g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17-8150_-17-8137d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316454 | ||||||
chr2:105316454
|
TGTGTGTG others(11): Show |
T | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-8154_-17-8137d others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316454 | ||||||
chr2:105316456
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0006t0009g0002 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-17-8150_-17-8139d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316456 | ||||||
chr2:105316456
|
TGTGTGTG others(9): Show |
T | 2 | a0001c0011t0014g0036a0002c0009t0005g0048 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-17-8154_-17-8139d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316456 | ||||||
chr2:105316458
|
T | C | 1 | a0002c0009t0005g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-17-8140A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | ||||||
chr2:105316458
|
TGTGTGCG others(3): Show |
T | 3 | a0001c0001t0001g0224a0001c0001t0001g0242a0002c0004t0005g0034 | 3 | HG03239.hp1 HG03453.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-17-8150_-17-8141d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | ||||||
chr2:105316458
|
TGTGTGCG others(5): Show |
T | 1 | a0002c0002t0002g0173 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-17-8152_-17-8141d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | ||||||
chr2:105316458
|
TGTGTGCG others(7): Show |
T | 3 | a0002c0004t0006g0218a0002c0004t0006g0219a0002c0004t0028g0220 | 3 | HG00735.hp2 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-17-8154_-17-8141d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | ||||||
chr2:105316458
|
TGTGTGCG others(9): Show |
T | 2 | a0001c0011t0014g0003a0001c0011t0014g0035 | 3 | HG02055.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-17-8156_-17-8141d others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316458 | ||||||
chr2:105316460
|
T | C | 2 | a0001c0003t0011g0291a0002c0009t0005g0050 | 2 | HG02451.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-17-8142A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316460
|
T | TGC | 3 | a0001c0003t0008g0330a0001c0003t0011g0320a0001c0003t0011g0343 | 3 | NA18968.hp1 NA18975.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-17-8143_-17-8142i others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316460
|
TGTGCGC | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0243 | 3 | HG04204.hp1 NA18951.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-17-8148_-17-8143d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316460
|
TGTGCGCG others(1): Show |
T | 4 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG02683.hp1 HG03017.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8150_-17-8143d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316460
|
TGTGCGCG others(3): Show |
T | 4 | a0002c0002t0002g0172a0002c0002t0021g0188a0002c0005t0003g0260others(1): Show | 4 | HG01261.hp1 HG02056.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8152_-17-8143d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316460
|
TGTGCGCG others(5): Show |
T | 6 | a0001c0006t0001g0169a0002c0002t0002g0132a0002c0002t0002g0168others(3): Show | 6 | HG00673.hp1 HG03669.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-8154_-17-8143d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316460 | ||||||
chr2:105316462
|
T | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 15 | HG00423.hp1 HG00741.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8144A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGC | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG02015.hp2 HG02818.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-8146_-17-8145d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGCGC | 5 | a0001c0003t0004g0319a0001c0003t0007g0318a0001c0003t0007g0334others(2): Show | 5 | HG00544.hp2 HG01074.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-8148_-17-8145d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGCGCGCG others(3): Show |
1 | a0001c0003t0034g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-17-8154_-17-8145d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGC | 8 | a0001c0001t0001g0113a0001c0001t0024g0114a0001c0003t0004g0283others(5): Show | 8 | HG00323.hp2 HG01123.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGCGC | 4 | a0001c0003t0004g0316a0001c0003t0008g0328a0001c0003t0011g0315others(1): Show | 4 | NA18945.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGCGCG others(3): Show |
2 | a0001c0003t0009g0126a0001c0003t0009g0221 | 2 | HG00140.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGCGCG others(5): Show |
1 | a0001c0003t0009g0023 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGCGCG others(7): Show |
2 | a0001c0003t0007g0346a0001c0003t0009g0127 | 2 | HG01516.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGCG others(5): Show |
1 | a0001c0003t0009g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGCG others(9): Show |
1 | a0002c0007t0037g0321 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(3): Show |
2 | a0001c0003t0008g0327a0001c0003t0024g0119 | 2 | NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(3): Show |
3 | a0001c0003t0007g0309a0001c0003t0041g0286a0002c0007t0003g0285 | 3 | HG02922.hp1 HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(5): Show |
2 | a0001c0003t0004g0284a0001c0003t0043g0363 | 2 | HG01175.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(5): Show |
1 | a0001c0003t0026g0360 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(7): Show |
1 | a0002c0007t0003g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316462
|
T | TGTGTGTG others(9): Show |
1 | a0001c0003t0026g0361 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-17-8145_-17-8144i others(18): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316462 | ||||||
chr2:105316464
|
C | T | 172 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0044others(169): Show | 180 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-17-8146G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316464 | ||||||
chr2:105316466
|
C | A | 1 | a0002c0004t0006g0007 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-17-8148G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316466 | ||||||
chr2:105316466
|
C | T | 63 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(60): Show | 63 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-17-8148G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316466 | ||||||
chr2:105316467
|
GCGCGCGC others(7): Show |
G | 2 | a0002c0012t0017g0010a0002c0012t0017g0263 | 3 | HG00639.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-17-8163_-17-8150d others(16): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316467 | ||||||
chr2:105316468
|
C | A | 2 | a0002c0004t0006g0214a0002c0004t0006g0215 | 2 | HG01261.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-17-8150G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316468 | ||||||
chr2:105316468
|
C | T | 18 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(15): Show | 18 | HG01109.hp1 HG02004.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-8150G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316468 | ||||||
chr2:105316469
|
G | A | 1 | a0001c0003t0004g0323 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-8151C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316469 | ||||||
chr2:105316469
|
GCGCGCGC others(5): Show |
G | 16 | a0001c0006t0001g0201a0002c0004t0003g0350a0002c0004t0006g0007others(13): Show | 17 | HG00673.hp2 HG01071.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8152d others(14): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316469 | ||||||
chr2:105316470
|
C | A | 7 | a0002c0004t0006g0008a0002c0004t0006g0205a0002c0004t0006g0206others(4): Show | 8 | HG00639.hp1 HG00741.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-8152G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316470 | ||||||
chr2:105316470
|
C | T | 9 | a0001c0006t0035g0139a0002c0002t0002g0134a0002c0002t0002g0138others(6): Show | 10 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-8152G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316470 | ||||||
chr2:105316471
|
GCGCGCGC others(3): Show |
G | 31 | a0001c0006t0004g0357a0002c0002t0002g0005a0002c0002t0002g0164others(28): Show | 33 | HG00280.hp2 HG00544.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8154d others(12): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316471 | ||||||
chr2:105316472
|
C | A | 3 | a0002c0004t0006g0207a0002c0004t0006g0209a0002c0004t0031g0208 | 3 | HG01934.hp1 HG02132.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-17-8154G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316472 | ||||||
chr2:105316473
|
G | A | 2 | a0002c0009t0005g0057a0002c0009t0018g0249 | 2 | HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8155C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316473 | ||||||
chr2:105316473
|
GCGCGCGC others(1): Show |
G | 43 | a0001c0001t0001g0122a0002c0002t0002g0001a0002c0002t0002g0004others(40): Show | 50 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8156d others(10): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316473 | ||||||
chr2:105316475
|
G | A | 6 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(3): Show | 6 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-8157C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316475 | ||||||
chr2:105316475
|
GCGCGCA | G | 23 | a0001c0001t0001g0225a0001c0006t0001g0148a0001c0006t0009g0033others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8158d others(8): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316475 | ||||||
chr2:105316477
|
GCGCA | G | 11 | a0001c0001t0001g0234a0001c0016t0001g0195a0002c0002t0002g0141others(8): Show | 11 | HG02004.hp1 HG02602.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8160d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316477 | ||||||
chr2:105316478
|
C | A | 5 | a0002c0004t0006g0216a0002c0004t0006g0217a0002c0004t0006g0218others(2): Show | 5 | HG00735.hp2 HG02004.hp2 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-8160G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316478 | ||||||
chr2:105316479
|
GCA | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0067others(20): Show | 23 | HG01070.hp1 HG02040.hp2 HG02165.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-8163_-17-8162d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316479 | ||||||
chr2:105316481
|
A | G | 135 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(132): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-17-8163T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316481 | ||||||
chr2:105316483
|
G | A | 1 | a0002c0022t0010g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-17-8165C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316483 | ||||||
chr2:105316483
|
G | GCGCGCGC others(11): Show |
1 | a0003c0014t0019g0348 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-17-8166_-17-8165i others(20): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316483 | ||||||
chr2:105316485
|
G | A | 27 | a0001c0003t0011g0322a0002c0005t0003g0258a0002c0005t0003g0259others(24): Show | 28 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-8167C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316485 | ||||||
chr2:105316509
|
T | C | 3 | a0002c0009t0005g0049a0002c0009t0005g0050a0002c0009t0005g0051 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-17-8191A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316509 | ||||||
chr2:105316684
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-17-8366G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316684 | ||||||
chr2:105316746
|
G | A | 1 | a0001c0003t0004g0323 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-17-8428C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316746 | ||||||
chr2:105316799
|
G | C | 2 | a0002c0002t0021g0175a0002c0002t0021g0188 | 2 | HG03942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-17-8481C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316799 | ||||||
chr2:105316813
|
C | CA | 17 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0206others(14): Show | 19 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-8496dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316813 | ||||||
chr2:105316813
|
CA | C | 7 | a0001c0003t0011g0291a0001c0003t0026g0360a0002c0004t0013g0190others(4): Show | 7 | HG02622.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-8496delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316813 | ||||||
chr2:105316862
|
C | G | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-8544G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105316862 | ||||||
chr2:105317080
|
C | CTTGTATG others(24): Show |
3 | a0001c0016t0001g0195a0002c0004t0005g0196a0002c0004t0005g0197 | 3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-17-8793_-17-8763d others(33): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317080 | ||||||
chr2:105317176
|
C | A | 2 | a0001c0003t0004g0283a0001c0003t0004g0284 | 2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-17-8858G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317176 | ||||||
chr2:105317176
|
C | T | 1 | a0002c0023t0003g0359 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-8858G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317176 | ||||||
chr2:105317201
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-8883C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317201 | ||||||
chr2:105317204
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-17-8886G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317204 | ||||||
chr2:105317272
|
A | G | 2 | a0001c0001t0001g0065a0001c0001t0027g0064 | 2 | NA18950.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-17-8954T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317272 | ||||||
chr2:105317329
|
C | T | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-9011G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317329 | ||||||
chr2:105317368
|
C | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0123others(5): Show | 9 | HG02055.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-9050G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317368 | ||||||
chr2:105317369
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG00408.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-17-9051C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317369 | ||||||
chr2:105317403
|
C | T | 5 | a0002c0002t0002g0134a0002c0002t0002g0135a0002c0002t0002g0136others(2): Show | 5 | NA18941.hp1 NA18981.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-9085G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317403 | ||||||
chr2:105317434
|
C | CA | 12 | a0001c0003t0007g0325a0001c0003t0007g0334a0001c0003t0008g0324others(9): Show | 12 | HG02015.hp2 HG02055.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17-9117dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317434 | ||||||
chr2:105317478
|
C | T | 1 | a0002c0002t0002g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-17-9160G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317478 | ||||||
chr2:105317554
|
A | C | 1 | a0002c0002t0002g0132 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-17-9236T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317554 | ||||||
chr2:105317611
|
A | G | 122 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(119): Show | 123 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-17-9293T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317611 | ||||||
chr2:105317764
|
G | C | 1 | a0002c0007t0003g0344 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-17-9446C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317764 | ||||||
chr2:105317844
|
T | C | 3 | a0002c0004t0005g0191a0002c0004t0005g0192a0002c0004t0005g0245 | 3 | HG03669.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-17-9526A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317844 | ||||||
chr2:105317998
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0227 | 4 | NA18950.hp1 NA18960.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-9680T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105317998 | ||||||
chr2:105318032
|
G | C | 1 | a0002c0002t0002g0176 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-17-9714C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318032 | ||||||
chr2:105318175
|
T | C | 1 | a0001c0001t0023g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-9857A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318175 | ||||||
chr2:105318354
|
C | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-17-10036G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318354 | ||||||
chr2:105318432
|
A | C | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-10114T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318432 | ||||||
chr2:105318709
|
A | G | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-10391T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318709 | ||||||
chr2:105318804
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-10486C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318804 | ||||||
chr2:105318822
|
G | T | 138 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(135): Show | 141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-17-10504C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105318822 | ||||||
chr2:105319027
|
C | A | 3 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350 | 4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+10598G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319027 | ||||||
chr2:105319031
|
G | A | 4 | a0001c0003t0007g0331a0001c0003t0007g0332a0001c0003t0007g0333others(1): Show | 4 | HG02056.hp1 NA18954.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+10594C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319031 | ||||||
chr2:105319065
|
T | G | 6 | a0001c0001t0001g0121a0002c0002t0002g0177a0002c0004t0003g0350others(3): Show | 6 | HG00642.hp2 HG01074.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+10560A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319065 | ||||||
chr2:105319067
|
G | T | 1 | a0001c0003t0004g0338 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18+10558C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319067 | ||||||
chr2:105319078
|
T | TGA | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+10545_-18+1054 others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319078 | ||||||
chr2:105319115
|
C | T | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+10510G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319115 | ||||||
chr2:105319223
|
G | A | 1 | a0001c0003t0007g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+10402C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319223 | ||||||
chr2:105319337
|
C | T | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+10288G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319337 | ||||||
chr2:105319418
|
G | A | 3 | a0001c0016t0001g0195a0002c0004t0005g0196a0002c0004t0005g0197 | 3 | HG03130.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18+10207C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319418 | ||||||
chr2:105319443
|
G | A | 2 | a0001c0008t0001g0017a0001c0008t0001g0018 | 2 | HG00558.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-18+10182C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319443 | ||||||
chr2:105319452
|
G | A | 2 | a0002c0002t0002g0178a0002c0002t0002g0179 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18+10173C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319452 | ||||||
chr2:105319624
|
G | A | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+10001C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319624 | ||||||
chr2:105319690
|
C | CA | 7 | a0001c0001t0023g0056a0001c0001t0023g0059a0001c0001t0029g0241others(4): Show | 7 | HG02809.hp2 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+9934dupT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319690 | ||||||
chr2:105319690
|
CA | C | 122 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(119): Show | 132 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-18+9934delT | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319690 | ||||||
chr2:105319939
|
A | C | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+9686T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319939 | ||||||
chr2:105319955
|
A | G | 287 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(284): Show | 301 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.-18+9670T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105319955 | ||||||
chr2:105320108
|
T | C | 4 | a0001c0010t0001g0040a0001c0010t0001g0041a0001c0010t0001g0060others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+9517A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320108 | ||||||
chr2:105320149
|
G | A | 3 | a0002c0002t0002g0180a0002c0002t0002g0181a0002c0002t0033g0182 | 3 | HG02071.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-18+9476C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320149 | ||||||
chr2:105320268
|
G | A | 1 | a0001c0008t0001g0019 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+9357C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320268 | ||||||
chr2:105320552
|
T | C | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+9073A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320552 | ||||||
chr2:105320653
|
C | A | 2 | a0002c0002t0022g0183a0002c0002t0022g0184 | 2 | NA18943.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-18+8972G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320653 | ||||||
chr2:105320964
|
A | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+8661T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105320964 | ||||||
chr2:105321027
|
C | T | 1 | a0002c0004t0005g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18+8598G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321027 | ||||||
chr2:105321069
|
T | C | 2 | a0001c0003t0007g0336a0001c0003t0007g0337 | 2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+8556A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321069 | ||||||
chr2:105321092
|
G | A | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+8533C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321092 | ||||||
chr2:105321153
|
C | CTTAT | 5 | a0002c0004t0003g0015a0002c0004t0003g0351a0002c0004t0005g0191others(2): Show | 6 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+8468_-18+8471d others(6): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321153 | ||||||
chr2:105321168
|
A | T | 8 | a0001c0003t0004g0283a0001c0003t0004g0284a0001c0003t0004g0288others(5): Show | 8 | HG01123.hp2 HG01175.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+8457T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321168 | ||||||
chr2:105321172
|
T | A | 269 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0026others(266): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-18+8453A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321172 | ||||||
chr2:105321176
|
T | A | 55 | a0001c0006t0001g0201a0001c0006t0001g0202a0001c0006t0001g0203others(52): Show | 60 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-18+8449A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321176 | ||||||
chr2:105321176
|
T | G | 1 | a0001c0006t0012g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18+8449A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321176 | ||||||
chr2:105321291
|
T | C | 4 | a0001c0006t0001g0202a0001c0006t0001g0203a0001c0006t0001g0204others(1): Show | 4 | HG02055.hp2 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+8334A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321291 | ||||||
chr2:105321387
|
C | T | 1 | a0001c0001t0015g0052 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-18+8238G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321387 | ||||||
chr2:105321457
|
C | T | 1 | a0002c0002t0002g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-18+8168G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321457 | ||||||
chr2:105321622
|
G | A | 1 | a0002c0002t0002g0189 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+8003C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321622 | ||||||
chr2:105321650
|
T | C | 285 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(282): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.-18+7975A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321650 | ||||||
chr2:105321732
|
A | C | 1 | a0002c0009t0005g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18+7893T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321732 | ||||||
chr2:105321797
|
G | T | 4 | a0002c0009t0005g0048a0002c0009t0005g0049a0002c0009t0005g0050others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7828C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321797 | ||||||
chr2:105321799
|
G | A | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7826C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321799 | ||||||
chr2:105321921
|
A | C | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+7704T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105321921 | ||||||
chr2:105322043
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-18+7582T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322043 | ||||||
chr2:105322243
|
TACA | T | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+7379_-18+7381d others(5): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322243 | ||||||
chr2:105322350
|
T | G | 1 | a0001c0001t0012g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18+7275A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322350 | ||||||
chr2:105322452
|
C | T | 3 | a0001c0011t0014g0003a0001c0011t0014g0035a0001c0011t0014g0036 | 4 | HG02055.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+7173G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322452 | ||||||
chr2:105322496
|
A | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+7129T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322496 | ||||||
chr2:105322533
|
T | C | 1 | a0001c0003t0007g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18+7092A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322533 | ||||||
chr2:105322579
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18+7046G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322579 | ||||||
chr2:105322694
|
G | C | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+6931C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322694 | ||||||
chr2:105322728
|
C | G | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0001c0011t0014g0003others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+6897G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322728 | ||||||
chr2:105322780
|
C | T | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+6845G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322780 | ||||||
chr2:105322841
|
A | C | 3 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350 | 4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6784T>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322841 | ||||||
chr2:105322900
|
C | G | 2 | a0001c0003t0004g0283a0001c0003t0004g0284 | 2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-18+6725G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322900 | ||||||
chr2:105322912
|
C | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+6713G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322912 | ||||||
chr2:105322973
|
C | T | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+6652G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105322973 | ||||||
chr2:105323212
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | NA18949.hp1 NA18968.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-18+6413G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323212 | ||||||
chr2:105323246
|
G | C | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0001c0011t0014g0003others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+6379C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323246 | ||||||
chr2:105323473
|
A | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | NA18612.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-18+6152T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323473 | ||||||
chr2:105323520
|
G | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+6105C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323520 | ||||||
chr2:105323578
|
G | A | 2 | a0003c0014t0019g0347a0003c0014t0019g0348 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+6047C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323578 | ||||||
chr2:105323989
|
T | C | 257 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(254): Show | 270 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.-18+5636A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323989 | ||||||
chr2:105323994
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-18+5631A>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105323994 | ||||||
chr2:105324002
|
C | A | 1 | a0002c0004t0018g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+5623G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324002 | ||||||
chr2:105324133
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18+5492C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324133 | ||||||
chr2:105324222
|
G | A | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+5403C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324222 | ||||||
chr2:105324482
|
G | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+5143C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324482 | ||||||
chr2:105324884
|
A | G | 1 | a0002c0004t0013g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18+4741T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324884 | ||||||
chr2:105324887
|
T | A | 1 | a0002c0023t0003g0359 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18+4738A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105324887 | ||||||
chr2:105325173
|
A | T | 138 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(135): Show | 141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-18+4452T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325173 | ||||||
chr2:105325230
|
ATGGATGG others(19): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+4369_-18+4394d others(28): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325230 | ||||||
chr2:105325331
|
C | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+4294G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325331 | ||||||
chr2:105325356
|
C | T | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+4269G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325356 | ||||||
chr2:105325466
|
A | T | 132 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(129): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.-18+4159T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325466 | ||||||
chr2:105325612
|
CTT | C | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+4011_-18+4012d others(4): Show |
TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325612 | ||||||
chr2:105325630
|
A | T | 3 | a0001c0006t0009g0002a0001c0006t0009g0033a0002c0004t0005g0034 | 4 | HG02109.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3995T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325630 | ||||||
chr2:105325632
|
C | T | 2 | a0001c0010t0001g0040a0001c0010t0001g0041 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-18+3993G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325632 | ||||||
chr2:105325793
|
C | G | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+3832G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325793 | ||||||
chr2:105325955
|
C | T | 1 | a0002c0005t0003g0258 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-18+3670G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105325955 | ||||||
chr2:105326055
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-18+3570A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326055 | ||||||
chr2:105326290
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0012g0248 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-18+3335T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326290 | ||||||
chr2:105326620
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-18+3005T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326620 | ||||||
chr2:105326668
|
G | A | 18 | a0002c0004t0006g0007a0002c0004t0006g0008a0002c0004t0006g0205others(15): Show | 20 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+2957C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326668 | ||||||
chr2:105326832
|
C | T | 3 | a0002c0004t0003g0014a0002c0004t0003g0349a0002c0004t0003g0350 | 4 | HG02257.hp1 HG02818.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2793G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326832 | ||||||
chr2:105326900
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18+2725A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326900 | ||||||
chr2:105326981
|
T | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+2644A>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326981 | ||||||
chr2:105326995
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-18+2630G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105326995 | ||||||
chr2:105327112
|
C | G | 68 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0035g0139others(65): Show | 74 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-18+2513G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327112 | ||||||
chr2:105327122
|
T | C | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-18+2503A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327122 | ||||||
chr2:105327128
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+2497G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327128 | ||||||
chr2:105327218
|
A | AT | 13 | a0001c0001t0001g0223a0001c0006t0004g0357a0002c0004t0003g0014others(10): Show | 14 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+2406dupA | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327218 | ||||||
chr2:105327375
|
G | A | 13 | a0001c0006t0004g0357a0002c0004t0003g0014a0002c0004t0003g0015others(10): Show | 15 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+2250C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327375 | ||||||
chr2:105327401
|
C | T | 1 | a0002c0002t0002g0130 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18+2224G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327401 | ||||||
chr2:105327409
|
A | T | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+2216T>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327409 | ||||||
chr2:105327438
|
C | T | 1 | a0002c0004t0032g0129 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+2187G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327438 | ||||||
chr2:105327442
|
C | A | 1 | a0001c0001t0001g0244 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-18+2183G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327442 | ||||||
chr2:105327590
|
C | A | 106 | a0001c0006t0001g0148a0001c0006t0001g0169a0001c0006t0001g0201others(103): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-18+2035G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327590 | ||||||
chr2:105327688
|
G | T | 3 | a0001c0003t0041g0286a0002c0007t0003g0285a0002c0007t0003g0287 | 3 | HG02257.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-18+1937C>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327688 | ||||||
chr2:105327737
|
G | C | 1 | a0001c0003t0009g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18+1888C>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327737 | ||||||
chr2:105327911
|
T | C | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+1714A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105327911 | ||||||
chr2:105328099
|
A | G | 6 | a0001c0006t0009g0002a0001c0006t0009g0033a0001c0011t0014g0003others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+1526T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328099 | ||||||
chr2:105328166
|
C | T | 1 | a0002c0002t0002g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-18+1459G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328166 | ||||||
chr2:105328242
|
T | C | 1 | a0002c0002t0002g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18+1383A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328242 | ||||||
chr2:105328272
|
T | C | 10 | a0001c0006t0004g0357a0002c0004t0003g0015a0002c0004t0003g0351others(7): Show | 11 | HG01070.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+1353A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328272 | ||||||
chr2:105328533
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0223a0001c0001t0001g0224others(20): Show | 24 | HG00408.hp1 HG01192.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18+1092C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328533 | ||||||
chr2:105328609
|
A | G | 1 | a0002c0004t0005g0031 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18+1016T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328609 | ||||||
chr2:105328619
|
C | G | 2 | a0001c0003t0004g0283a0001c0003t0004g0284 | 2 | HG01123.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-18+1006G>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328619 | ||||||
chr2:105328671
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+954G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105328671 | ||||||
chr2:105329011
|
T | C | 2 | a0002c0005t0010g0281a0002c0005t0010g0282 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-18+614A>G | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329011 | ||||||
chr2:105329379
|
G | A | 3 | a0001c0008t0001g0020a0001c0008t0001g0021a0001c0008t0001g0022 | 3 | NA18977.hp1 NA19000.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-18+246C>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329379 | ||||||
chr2:105329394
|
C | T | 28 | a0002c0005t0003g0258a0002c0005t0003g0259a0002c0005t0003g0260others(25): Show | 29 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18+231G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329394 | ||||||
chr2:105329432
|
C | A | 1 | a0002c0004t0005g0245 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-18+193G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329432 | ||||||
chr2:105329455
|
C | A | 1 | a0002c0002t0002g0246 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-18+170G>T | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329455 | ||||||
chr2:105329520
|
A | G | 1 | a0001c0003t0009g0023 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-18+105T>C | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329520 | ||||||
chr2:105329559
|
C | T | 7 | a0001c0008t0001g0016a0001c0008t0001g0017a0001c0008t0001g0018others(4): Show | 7 | HG00558.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+66G>A | TGFBRAP1 | ENSG00000135966.14 | transcript | ENST00000393359.7 | protein_coding | 1/11 | chr2 | 105329559 |