geneid | 5781 |
---|---|
ensemblid | ENSG00000179295.19 |
hgncid | 9644 |
symbol | PTPN11 |
name | protein tyrosine phosphatase non-receptor type 11 |
refseq_nuc | NM_002834.5 |
refseq_prot | NP_002825.3 |
ensembl_nuc | ENST00000351677.7 |
ensembl_prot | ENSP00000340944.3 |
mane_status | MANE Select |
chr | chr12 |
start | 112418947 |
end | 112509918 |
strand | + |
ver | v1.2 |
region | chr12:112418947-112509918 |
region5000 | chr12:112413947-112514918 |
regionname0 | PTPN11_chr12_112418947_112509918 |
regionname5000 | PTPN11_chr12_112413947_112514918 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 593 | 298 | 84 | 46 | 133 | 6 | 27 | 110 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0002 | 0/0 | 593 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0003 | 0/0 | 593 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1782 | 287 | 73 | 46 | 133 | 6 | 27 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
c0002 | 0/0 | 1782 | 11 | 11 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
c0003 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
c0004 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4289 | 125 | 52 | 12 | 52 | 1 | 8 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0002 | 0/0 | 4283 | 78 | 7 | 13 | 54 | 1 | 3 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0003 | 1/1 | 4292 | 61 | 6 | 18 | 18 | 3 | 14 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0004 | 0/0 | 4286 | 7 | 5 | 1 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0005 | 0/0 | 4286 | 6 | 6 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0006 | 0/0 | 4288 | 5 | 2 | 2 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0007 | 0/0 | 4289 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0008 | 0/0 | 4268 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0009 | 0/0 | 4286 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0010 | 0/0 | 4289 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0011 | 0/0 | 4292 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0012 | 0/0 | 4289 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0013 | 0/0 | 4292 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0014 | 0/0 | 4292 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0015 | 0/0 | 4292 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0016 | 0/0 | 4292 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0017 | 0/0 | 4289 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0018 | 0/0 | 4286 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0019 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0020 | 0/0 | 4268 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0021 | 0/0 | 4289 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
t0022 | 0/0 | 4289 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1782 | 287 | 73 | 46 | 133 | 6 | 27 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0002 | 0/0 | 1782 | 11 | 11 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0002c0003 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0003c0004 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6070 | 114 | 41 | 12 | 52 | 1 | 8 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0002 | 0/0 | 6064 | 78 | 7 | 13 | 54 | 1 | 3 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0003 | 1/1 | 6073 | 59 | 6 | 18 | 17 | 3 | 13 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0004 | 0/0 | 6067 | 7 | 5 | 1 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0005 | 0/0 | 6067 | 6 | 6 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0006 | 0/0 | 6069 | 5 | 2 | 2 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0007 | 0/0 | 6070 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0008 | 0/0 | 6049 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0009 | 0/0 | 6067 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0010 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0011 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0012 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0013 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0014 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0015 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0016 | 0/0 | 6073 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0017 | 0/0 | 6070 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0018 | 0/0 | 6067 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0019 | 0/0 | 6064 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0020 | 0/0 | 6049 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0021 | 0/0 | 6070 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0001t0022 | 0/0 | 6070 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0001c0002t0001 | 0/0 | 6070 | 11 | 11 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0002c0003t0003 | 0/0 | 6073 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
a0003c0004t0003 | 0/0 | 6073 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | copy fasta | chr12 | 112413947 | 112514918 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0014g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0017g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0019g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0020g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0021g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0001t0022g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0002c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
a0003c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0095 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0206 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0184 | EUR | GBR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0208 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02056 | hp2 | a0003 | c0004 | t0003 | g0173 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | CDX | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02280 | hp2 | a0001 | c0001 | t0021 | g0143 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02523 | hp2 | a0001 | c0001 | t0010 | g0153 | EAS | KHV | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0207 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03017 | hp1 | a0002 | c0003 | t0003 | g0186 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03195 | hp2 | a0001 | c0001 | t0018 | g0049 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03704 | hp1 | a0001 | c0001 | t0016 | g0142 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03831 | hp2 | a0001 | c0001 | t0022 | g0279 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | STU | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18994 | hp2 | a0001 | c0001 | t0015 | g0182 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19002 | hp2 | a0001 | c0001 | t0019 | g0249 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19004 | hp1 | a0001 | c0001 | t0014 | g0141 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19057 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19070 | hp1 | a0001 | c0001 | t0017 | g0070 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19076 | hp2 | a0001 | c0001 | t0012 | g0222 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19079 | hp1 | a0001 | c0001 | t0013 | g0175 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19083 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19086 | hp1 | a0001 | c0001 | t0020 | g0238 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ASW | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ASW | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0185 | EUR | TSI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | GIH | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | GIH | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | USA | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | USA | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | LWK | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0131 | REF | REF | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0156 | REF | REF | PTPN11_chr12_112413947_112514918 | PTPN11 | chr12 | 112413947 | 112514918 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:112477951
|
G | A | 1 | a0002 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1028G>A | p.Arg343Gln | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/16 | 1193/6073 | 1028/1782 | 343/593 | chr12 | 112477951 | ||
chr12:112504711
|
G | A | 1 | a0003 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1729G>A | p.Ala577Thr | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/16 | 1894/6073 | 1729/1782 | 577/593 | chr12 | 112504711 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:112450435
|
C | T | 1 | a0001c0002 | 11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.255C>T | p.His85His | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/16 | 420/6073 | 255/1782 | 85/593 | chr12 | 112450435 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:112418991
|
G | T | 1 | a0001c0001t0022 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/16 | chr12 | 112418991 | ||||||
chr12:112505898
|
ATTTGGAA others(11): Show |
A | 1 | a0001c0001t0008 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108_*125delTTGGAA others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1136 | INFO_REALIGN_3_PRIME | chr12 | 112505898 | ||||
chr12:112505967
|
G | T | 1 | a0001c0001t0021 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1203 | chr12 | 112505967 | |||||
chr12:112506097
|
G | A | 1 | a0001c0001t0009 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1333 | chr12 | 112506097 | |||||
chr12:112506121
|
T | C | 1 | a0001c0001t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*329T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1357 | chr12 | 112506121 | |||||
chr12:112506462
|
G | A | 1 | a0001c0001t0007 | 3 | HG03516.hp1 HG03540.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1698 | chr12 | 112506462 | |||||
chr12:112506630
|
G | A | 1 | a0001c0001t0011 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 1866 | chr12 | 112506630 | |||||
chr12:112506797
|
CG | C | 1 | a0001c0001t0006 | 5 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1006delG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2034 | chr12 | 112506797 | |||||
chr12:112506927
|
T | G | 1 | a0001c0001t0012 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1135T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2163 | chr12 | 112506927 | |||||
chr12:112506946
|
TTGA | T | 9 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(6): Show | 138 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1199_*1201delATG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2227 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | ||||
chr12:112506946
|
TTGATGA | T | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(2): Show | 16 | HG01109.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1196_*1201delATGA others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2224 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | ||||
chr12:112506946
|
TTGATGAT others(2): Show |
T | 2 | a0001c0001t0002a0001c0001t0019 | 79 | HG00140.hp1 HG00544.hp2 HG00735.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1193_*1201delATGA others(5): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2221 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | ||||
chr12:112506946
|
TTGATGAT others(17): Show |
T | 1 | a0001c0001t0020 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1201delATGA others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2206 | INFO_REALIGN_3_PRIME | chr12 | 112506946 | ||||
chr12:112507166
|
G | C | 1 | a0001c0001t0005 | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1374G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 2402 | chr12 | 112507166 | |||||
chr12:112507921
|
A | G | 1 | a0001c0001t0019 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2129A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3157 | chr12 | 112507921 | |||||
chr12:112508244
|
G | A | 1 | a0001c0001t0013 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2452G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3480 | chr12 | 112508244 | |||||
chr12:112508514
|
T | C | 1 | a0001c0001t0014 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2722T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3750 | chr12 | 112508514 | |||||
chr12:112508719
|
T | A | 1 | a0001c0001t0018 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2927T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 3955 | chr12 | 112508719 | |||||
chr12:112509173
|
A | G | 1 | a0001c0001t0016 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4409 | chr12 | 112509173 | |||||
chr12:112509294
|
A | G | 1 | a0001c0001t0017 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4530 | chr12 | 112509294 | |||||
chr12:112509330
|
T | C | 1 | a0001c0001t0015 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 16/16 | 4566 | chr12 | 112509330 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:112419150
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 21 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.14+25G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419150 | ||||||
chr12:112419179
|
C | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+54C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419179 | ||||||
chr12:112419232
|
C | G | 1 | a0001c0001t0002g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.14+107C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419232 | ||||||
chr12:112419571
|
G | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+446G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419571 | ||||||
chr12:112419858
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.14+733C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112419858 | ||||||
chr12:112420727
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+1602G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112420727 | ||||||
chr12:112420954
|
A | AG | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+1831dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112420954 | |||||
chr12:112421093
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.14+1968T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112421093 | ||||||
chr12:112422061
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+2936G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422061 | ||||||
chr12:112422078
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+2953T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422078 | ||||||
chr12:112422309
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+3184T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422309 | ||||||
chr12:112422625
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | NA18992.hp1 NA19065.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.14+3500G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112422625 | ||||||
chr12:112423112
|
A | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+3987A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423112 | ||||||
chr12:112423726
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.14+4601C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423726 | ||||||
chr12:112423740
|
C | CT | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 23 | HG01109.hp2 HG01934.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.14+4637dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112423740 | |||||
chr12:112423740
|
CT | C | 10 | a0001c0001t0001g0032a0001c0001t0002g0040a0001c0001t0002g0041others(7): Show | 10 | HG01109.hp1 HG01256.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.14+4637delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112423740 | |||||
chr12:112423805
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0004g0033 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.14+4680G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112423805 | ||||||
chr12:112424098
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+4973C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424098 | ||||||
chr12:112424402
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.14+5277T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424402 | ||||||
chr12:112424855
|
A | G | 9 | a0001c0001t0002g0041a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5730A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424855 | ||||||
chr12:112424867
|
T | TTG | 22 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0195others(19): Show | 23 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+5764_14+5765dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424867 | |||||
chr12:112424877
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0280 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.14+5766_14+5779del others(14): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424877 | |||||
chr12:112424881
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.14+5766_14+5775del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424881 | |||||
chr12:112424883
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424883 | |||||
chr12:112424885
|
G | GTGTGTGT others(1): Show |
7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 8 | HG02145.hp2 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424885 | |||||
chr12:112424885
|
GTGTGTA | G | 41 | a0001c0001t0001g0211a0001c0001t0002g0001a0001c0001t0002g0005others(38): Show | 48 | HG00544.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.14+5766_14+5771del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424885 | |||||
chr12:112424887
|
GTGTA | G | 20 | a0001c0001t0001g0250a0001c0001t0002g0040a0001c0001t0002g0041others(17): Show | 20 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.14+5766_14+5769del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424887 | |||||
chr12:112424889
|
G | GTGTA | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+5765_14+5766ins others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424889 | |||||
chr12:112424889
|
GTA | G | 8 | a0001c0001t0001g0256a0001c0001t0002g0257a0001c0001t0002g0258others(5): Show | 8 | HG01928.hp2 HG01952.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+5766_14+5767del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424889 | |||||
chr12:112424891
|
A | ATG | 22 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0187others(19): Show | 22 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.14+5793_14+5794dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424891 | |||||
chr12:112424891
|
A | G | 19 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 20 | HG00621.hp2 HG01258.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+5766A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424891 | ||||||
chr12:112424893
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.14+5768G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424893 | ||||||
chr12:112424916
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.14+5791T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424916 | ||||||
chr12:112424942
|
CCAT | C | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+5818_14+5820del others(3): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112424942 | ||||||
chr12:112424956
|
T | TTG | 13 | a0001c0001t0001g0025a0001c0001t0003g0164a0001c0001t0003g0165others(10): Show | 13 | HG02056.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+5883_14+5884dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
T | TTGTG | 7 | a0001c0001t0001g0043a0001c0001t0001g0174a0001c0001t0001g0289others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+5881_14+5884dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTG | T | 49 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(46): Show | 49 | HG00140.hp1 HG00735.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.14+5883_14+5884del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTG | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0097a0001c0001t0001g0098others(70): Show | 81 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.14+5881_14+5884del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTG | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0074others(39): Show | 43 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.14+5879_14+5884del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(1): Show |
T | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG02257.hp2 HG02922.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+5877_14+5884del others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG02027.hp1 HG02055.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5875_14+5884del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(5): Show |
T | 13 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 13 | HG01993.hp2 HG02074.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+5873_14+5884del others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0052a0001c0001t0003g0051 | 2 | HG01071.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.14+5869_14+5884del others(16): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0050a0001c0001t0018g0049 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.14+5865_14+5884del others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0004g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14+5863_14+5884del others(22): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112424956
|
TTGTGTGT others(21): Show |
T | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+5857_14+5884del others(28): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112424956 | |||||
chr12:112425000
|
G | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0017 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.14+5875G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425000 | ||||||
chr12:112425002
|
G | A | 6 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0005g0018others(3): Show | 6 | HG02622.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+5877G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425002 | ||||||
chr12:112425004
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0003g0002a0001c0001t0004g0024others(1): Show | 5 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5879G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425004 | ||||||
chr12:112425004
|
GTGTGTA | G | 6 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0005g0018others(3): Show | 6 | HG02622.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+5883_14+5888del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425004 | |||||
chr12:112425006
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5881G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425006 | ||||||
chr12:112425006
|
GTGTA | G | 4 | a0001c0001t0001g0007a0001c0001t0003g0002a0001c0001t0004g0024others(1): Show | 5 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5886_14+5889del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425006 | |||||
chr12:112425008
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0014 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.14+5883G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425008 | ||||||
chr12:112425008
|
GTA | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+5885_14+5886del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112425008 | |||||
chr12:112425010
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0014 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.14+5885A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425010 | ||||||
chr12:112425202
|
T | C | 1 | a0001c0001t0003g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.14+6077T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425202 | ||||||
chr12:112425318
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.14+6193G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425318 | ||||||
chr12:112425347
|
A | G | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.14+6222A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425347 | ||||||
chr12:112425755
|
G | A | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+6630G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425755 | ||||||
chr12:112425793
|
A | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+6668A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425793 | ||||||
chr12:112425943
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.14+6818C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112425943 | ||||||
chr12:112426224
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+7099G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426224 | ||||||
chr12:112426298
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+7173G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426298 | ||||||
chr12:112426512
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0003g0137 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.14+7387C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426512 | ||||||
chr12:112426685
|
T | A | 1 | a0001c0001t0002g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.14+7560T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112426685 | ||||||
chr12:112427071
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.14+7946C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427071 | ||||||
chr12:112427201
|
G | A | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+8076G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427201 | ||||||
chr12:112427294
|
C | G | 1 | a0001c0001t0022g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.14+8169C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427294 | ||||||
chr12:112427494
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+8369C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427494 | ||||||
chr12:112427545
|
C | CA | 7 | a0001c0001t0001g0097a0001c0001t0005g0016a0001c0001t0005g0017others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+8432dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112427545 | |||||
chr12:112427759
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.14+8634T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427759 | ||||||
chr12:112427774
|
C | A | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.14+8649C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427774 | ||||||
chr12:112427827
|
T | C | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.14+8702T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427827 | ||||||
chr12:112427888
|
C | T | 16 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(13): Show | 16 | HG01993.hp2 HG02135.hp2 HG03710.hp2 others(13): Show |
intron_variant | MODIFIER | c.14+8763C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427888 | ||||||
chr12:112427898
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+8773G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427898 | ||||||
chr12:112427996
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 182 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(179): Show |
intron_variant | MODIFIER | c.14+8871T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112427996 | ||||||
chr12:112428029
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+8904G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428029 | ||||||
chr12:112428396
|
CT | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 186 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(183): Show |
intron_variant | MODIFIER | c.14+9292delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112428396 | |||||
chr12:112428526
|
T | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14+9401T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428526 | ||||||
chr12:112428651
|
GA | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0096a0001c0001t0001g0158others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+9536delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112428651 | |||||
chr12:112428652
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+9527A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428652 | ||||||
chr12:112428872
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+9747C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112428872 | ||||||
chr12:112429027
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14+9902G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429027 | ||||||
chr12:112429094
|
A | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.14+9969A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429094 | ||||||
chr12:112429125
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14+10000A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429125 | ||||||
chr12:112429481
|
C | CT | 25 | a0001c0001t0001g0032a0001c0001t0001g0072a0001c0001t0001g0089others(22): Show | 25 | HG00735.hp2 HG01071.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.14+10381dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | |||||
chr12:112429481
|
C | CTT | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0019others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+10380_14+10381d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | |||||
chr12:112429481
|
CT | C | 13 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0045others(10): Show | 13 | HG01167.hp1 HG01943.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+10381delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112429481 | |||||
chr12:112429552
|
C | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.14+10427C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429552 | ||||||
chr12:112429575
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.14+10450A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429575 | ||||||
chr12:112429795
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.14+10670T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429795 | ||||||
chr12:112429865
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.14+10740G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429865 | ||||||
chr12:112429951
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14+10826G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429951 | ||||||
chr12:112429972
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.14+10847T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112429972 | ||||||
chr12:112430163
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.14+11038G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430163 | ||||||
chr12:112430320
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.14+11195A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430320 | ||||||
chr12:112430330
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.14+11205C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430330 | ||||||
chr12:112430625
|
A | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+11500A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430625 | ||||||
chr12:112430752
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.14+11627G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112430752 | ||||||
chr12:112431022
|
G | T | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.14+11897G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431022 | ||||||
chr12:112431075
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.14+11950G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431075 | ||||||
chr12:112431265
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.14+12140G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431265 | ||||||
chr12:112431288
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.14+12163C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431288 | ||||||
chr12:112431572
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.14+12447C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431572 | ||||||
chr12:112431761
|
C | G | 1 | a0001c0001t0002g0252 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.14+12636C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431761 | ||||||
chr12:112431892
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.14+12767C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431892 | ||||||
chr12:112431926
|
TAA | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.14+12805_14+12806d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112431926 | |||||
chr12:112431931
|
AG | A | 5 | a0001c0001t0001g0098a0001c0001t0002g0213a0001c0001t0002g0214others(2): Show | 5 | NA18947.hp1 NA18960.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+12812delG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112431931 | |||||
chr12:112431976
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+12851A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112431976 | ||||||
chr12:112432051
|
A | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+12926A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432051 | ||||||
chr12:112432098
|
T | C | 3 | a0001c0001t0003g0073a0001c0001t0003g0120a0001c0001t0003g0121 | 3 | NA18984.hp2 NA18986.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.14+12973T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432098 | ||||||
chr12:112432204
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0109a0001c0001t0001g0139 | 3 | NA18971.hp1 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.14+13079A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432204 | ||||||
chr12:112432537
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.14+13412C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432537 | ||||||
chr12:112432593
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.14+13468C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432593 | ||||||
chr12:112432668
|
C | CA | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0055others(14): Show | 17 | HG01993.hp2 HG02135.hp2 HG02738.hp1 others(14): Show |
intron_variant | MODIFIER | c.14+13561dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112432668 | |||||
chr12:112432668
|
CA | C | 7 | a0001c0001t0003g0073a0001c0001t0003g0183a0001c0001t0004g0024others(4): Show | 7 | HG02897.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+13561delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112432668 | |||||
chr12:112432813
|
C | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-13463C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432813 | ||||||
chr12:112432866
|
T | C | 6 | a0001c0001t0001g0145a0001c0001t0006g0135a0001c0001t0006g0205others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-13410T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432866 | ||||||
chr12:112432941
|
A | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15-13335A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112432941 | ||||||
chr12:112433094
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.15-13182C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433094 | ||||||
chr12:112433108
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.15-13168G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433108 | ||||||
chr12:112433372
|
C | G | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-12904C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433372 | ||||||
chr12:112433538
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0087 | 4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-12738A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433538 | ||||||
chr12:112433568
|
A | G | 17 | a0001c0001t0002g0128a0001c0001t0003g0038a0001c0001t0003g0095others(14): Show | 17 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-12708A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433568 | ||||||
chr12:112433780
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15-12496A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433780 | ||||||
chr12:112433831
|
T | C | 1 | a0001c0001t0005g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-12445T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112433831 | ||||||
chr12:112434236
|
C | T | 1 | a0001c0001t0003g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.15-12040C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434236 | ||||||
chr12:112434606
|
C | CA | 8 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0218others(5): Show | 8 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-11656dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112434606 | |||||
chr12:112434606
|
CA | C | 6 | a0001c0001t0001g0174a0001c0001t0003g0038a0001c0001t0003g0154others(3): Show | 6 | HG01256.hp2 HG02622.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-11656delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112434606 | |||||
chr12:112434717
|
C | T | 1 | a0001c0001t0005g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-11559C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434717 | ||||||
chr12:112434955
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15-11321T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112434955 | ||||||
chr12:112435183
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(2): Show | 5 | NA18946.hp1 NA18950.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-11093C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435183 | ||||||
chr12:112435287
|
T | C | 1 | a0001c0001t0005g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15-10989T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435287 | ||||||
chr12:112435419
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.15-10857C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435419 | ||||||
chr12:112435422
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.15-10854T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112435422 | ||||||
chr12:112435647
|
G | GT | 98 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 99 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.15-10610dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | |||||
chr12:112435647
|
G | GTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 16 | HG01167.hp1 HG01361.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.15-10611_15-10610d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | |||||
chr12:112435647
|
GT | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0052others(10): Show | 13 | HG01978.hp2 HG02257.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-10610delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112435647 | |||||
chr12:112436214
|
T | G | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(25): Show | 28 | HG00140.hp2 HG00738.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.15-10062T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436214 | ||||||
chr12:112436375
|
A | G | 6 | a0001c0001t0001g0145a0001c0001t0006g0135a0001c0001t0006g0205others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-9901A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436375 | ||||||
chr12:112436407
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15-9869C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436407 | ||||||
chr12:112436501
|
T | A | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-9775T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436501 | ||||||
chr12:112436781
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.15-9495C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436781 | ||||||
chr12:112436937
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.15-9339G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112436937 | ||||||
chr12:112437085
|
T | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-9191T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437085 | ||||||
chr12:112437089
|
C | T | 2 | a0001c0001t0003g0168a0001c0001t0013g0175 | 2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.15-9187C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437089 | ||||||
chr12:112437313
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15-8963G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437313 | ||||||
chr12:112437381
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0003g0137 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.15-8895G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437381 | ||||||
chr12:112437779
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15-8497T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437779 | ||||||
chr12:112437888
|
A | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-8388A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437888 | ||||||
chr12:112437959
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0176 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.15-8317C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112437959 | ||||||
chr12:112438287
|
G | A | 1 | a0001c0001t0005g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.15-7989G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438287 | ||||||
chr12:112438615
|
G | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0100others(1): Show | 4 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-7661G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438615 | ||||||
chr12:112438850
|
C | A | 3 | a0001c0001t0001g0277a0001c0001t0007g0116a0001c0001t0007g0199 | 3 | HG03098.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15-7426C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438850 | ||||||
chr12:112438932
|
G | GT | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(64): Show | 69 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.15-7339dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112438932 | |||||
chr12:112438950
|
T | C | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-7326T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112438950 | ||||||
chr12:112439215
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-7061C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439215 | ||||||
chr12:112439243
|
C | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-7033C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439243 | ||||||
chr12:112439280
|
T | A | 1 | a0001c0002t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15-6996T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439280 | ||||||
chr12:112439500
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-6776G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439500 | ||||||
chr12:112439784
|
T | A | 7 | a0001c0001t0001g0027a0001c0001t0002g0257a0001c0001t0002g0259others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-6492T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439784 | ||||||
chr12:112439785
|
A | T | 8 | a0001c0001t0001g0145a0001c0001t0003g0126a0001c0001t0006g0135others(5): Show | 8 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6491A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439785 | ||||||
chr12:112439790
|
A | C | 6 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0265others(3): Show | 6 | HG01258.hp1 HG01496.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-6486A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439790 | ||||||
chr12:112439792
|
A | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-6484A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439792 | ||||||
chr12:112439795
|
AC | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0002g0210others(3): Show | 6 | HG03516.hp1 NA18960.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-6480delC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439795 | ||||||
chr12:112439796
|
C | A | 224 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 234 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.15-6480C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439796 | ||||||
chr12:112439797
|
A | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-6479A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112439797 | ||||||
chr12:112440464
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.15-5812C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440464 | ||||||
chr12:112440563
|
C | CT | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.15-5685dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | |||||
chr12:112440563
|
C | CTT | 7 | a0001c0001t0001g0080a0001c0001t0001g0288a0001c0001t0001g0289others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-5686_15-5685dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | |||||
chr12:112440563
|
CT | C | 10 | a0001c0001t0002g0041a0001c0001t0002g0267a0001c0001t0002g0268others(7): Show | 10 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-5685delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440563 | |||||
chr12:112440622
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-5654G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440622 | ||||||
chr12:112440626
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15-5650C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440626 | ||||||
chr12:112440698
|
C | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-5578C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440698 | ||||||
chr12:112440920
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15-5356T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440920 | ||||||
chr12:112440965
|
C | CT | 8 | a0001c0001t0002g0218a0001c0001t0002g0230a0001c0001t0002g0231others(5): Show | 8 | HG00735.hp1 HG02622.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-5295dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440965 | |||||
chr12:112440965
|
CT | C | 12 | a0001c0001t0001g0050a0001c0001t0001g0289a0001c0001t0002g0221others(9): Show | 12 | HG01168.hp1 HG01256.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-5295delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112440965 | |||||
chr12:112440969
|
T | TC | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-5307_15-5306ins others(1): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112440969 | ||||||
chr12:112441007
|
A | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-5269A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441007 | ||||||
chr12:112441019
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-5257A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441019 | ||||||
chr12:112441042
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.15-5234G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441042 | ||||||
chr12:112441113
|
C | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-5163C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441113 | ||||||
chr12:112441143
|
T | C | 1 | a0001c0001t0004g0024 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.15-5133T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441143 | ||||||
chr12:112441550
|
A | C | 1 | a0001c0001t0002g0285 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.15-4726A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112441550 | ||||||
chr12:112442068
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.15-4208C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442068 | ||||||
chr12:112442151
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 21 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-4125A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442151 | ||||||
chr12:112442315
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.15-3961T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442315 | ||||||
chr12:112442704
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-3572C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442704 | ||||||
chr12:112442742
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.15-3534G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442742 | ||||||
chr12:112442775
|
T | C | 11 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-3501T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442775 | ||||||
chr12:112442830
|
T | TTA | 12 | a0001c0001t0001g0031a0001c0001t0001g0052a0001c0001t0003g0120others(9): Show | 12 | HG00544.hp1 HG01978.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-3399_15-3398dup others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATA | 12 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0043others(9): Show | 12 | HG00140.hp2 HG01167.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-3401_15-3398dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATATA | 5 | a0001c0001t0001g0115a0001c0001t0003g0123a0001c0001t0014g0141others(2): Show | 5 | HG02683.hp2 HG03017.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-3403_15-3398dup others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0003g0134others(1): Show | 4 | HG00738.hp1 HG01361.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-3405_15-3398dup others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0003g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15-3407_15-3398dup others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATATAT others(5): Show |
3 | a0001c0001t0003g0038a0001c0001t0003g0114a0001c0001t0003g0177 | 3 | HG01256.hp2 HG01433.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.15-3409_15-3398dup others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0003g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.15-3417_15-3398dup others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTA | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0179others(14): Show | 17 | HG00140.hp1 HG01928.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.15-3399_15-3398del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATA | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0058others(14): Show | 17 | HG00099.hp2 HG00741.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.15-3401_15-3398del others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATA | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0057others(7): Show | 10 | HG02559.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-3403_15-3398del others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(1): Show |
T | 18 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0030others(15): Show | 18 | HG01099.hp2 HG01109.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.15-3405_15-3398del others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0001g0050a0001c0001t0001g0277a0001c0001t0004g0286others(2): Show | 5 | HG02559.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-3407_15-3398del others(10): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0018g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.15-3409_15-3398del others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(9): Show |
T | 1 | a0001c0001t0003g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.15-3413_15-3398del others(16): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(11): Show |
T | 6 | a0001c0001t0001g0066a0001c0001t0001g0097a0001c0001t0001g0099others(3): Show | 6 | HG02738.hp1 HG02922.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-3415_15-3398del others(18): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(13): Show |
T | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(66): Show | 71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.15-3417_15-3398del others(20): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(19): Show |
T | 2 | a0001c0001t0002g0239a0001c0001t0003g0126 | 2 | HG02165.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.15-3423_15-3398del others(26): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(21): Show |
T | 72 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(69): Show | 79 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.15-3425_15-3398del others(28): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(23): Show |
T | 3 | a0001c0001t0001g0025a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01168.hp1 HG01169.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.15-3427_15-3398del others(30): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(25): Show |
T | 1 | a0001c0001t0003g0264 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.15-3429_15-3398del others(32): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442830
|
TTATATAT others(29): Show |
T | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-3433_15-3398del others(36): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442830 | |||||
chr12:112442859
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15-3408_15-3407ins others(25): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442859 | |||||
chr12:112442859
|
T | TATATATA others(22): Show |
1 | a0001c0001t0001g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15-3402_15-3401ins others(29): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442859 | |||||
chr12:112442877
|
T | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(71): Show | 76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.15-3399T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112442877 | ||||||
chr12:112442877
|
T | TATAA | 2 | a0001c0001t0003g0002a0001c0001t0005g0019 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.15-3398_15-3397ins others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442877 | |||||
chr12:112442902
|
A | ATGTATGT others(2): Show |
167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(164): Show | 177 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(174): Show |
intron_variant | MODIFIER | c.15-3373_15-3365dup others(9): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112442902 | |||||
chr12:112443026
|
A | G | 3 | a0001c0001t0006g0135a0001c0001t0006g0205a0001c0001t0006g0207 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.15-3250A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443026 | ||||||
chr12:112443505
|
T | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(71): Show | 76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.15-2771T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443505 | ||||||
chr12:112443538
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(168): Show | 181 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(178): Show |
intron_variant | MODIFIER | c.15-2738G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443538 | ||||||
chr12:112443653
|
C | CT | 27 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 29 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.15-2606dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112443653 | |||||
chr12:112443715
|
T | C | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-2561T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443715 | ||||||
chr12:112443733
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.15-2543A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443733 | ||||||
chr12:112443845
|
G | C | 1 | a0001c0001t0003g0140 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.15-2431G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112443845 | ||||||
chr12:112444069
|
G | C | 11 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-2207G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444069 | ||||||
chr12:112444071
|
G | A | 1 | a0001c0001t0011g0146 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.15-2205G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444071 | ||||||
chr12:112444107
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.15-2169C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444107 | ||||||
chr12:112444119
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-2157G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444119 | ||||||
chr12:112444128
|
A | G | 1 | a0001c0001t0003g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15-2148A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444128 | ||||||
chr12:112444140
|
T | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0100others(1): Show | 4 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-2136T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444140 | ||||||
chr12:112444192
|
A | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(66): Show | 71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.15-2084A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444192 | ||||||
chr12:112444490
|
C | T | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-1786C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444490 | ||||||
chr12:112444491
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.15-1785G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444491 | ||||||
chr12:112444591
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.15-1685C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444591 | ||||||
chr12:112444679
|
A | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0004g0033 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-1597A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112444679 | ||||||
chr12:112445041
|
ATG | A | 6 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0260others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-1221_15-1220del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112445041 | |||||
chr12:112445055
|
G | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 14 | HG02132.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.15-1221G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445055 | ||||||
chr12:112445262
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0004g0033 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-1014G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445262 | ||||||
chr12:112445336
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.15-940T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445336 | ||||||
chr12:112445339
|
C | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.15-937C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445339 | ||||||
chr12:112445636
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.15-640A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445636 | ||||||
chr12:112445639
|
C | CT | 7 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0091others(4): Show | 7 | HG00621.hp1 HG01993.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.15-620dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 112445639 | |||||
chr12:112445664
|
T | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.15-612T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445664 | ||||||
chr12:112445672
|
G | A | 14 | a0001c0001t0003g0038a0001c0001t0003g0095a0001c0001t0003g0114others(11): Show | 14 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.15-604G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445672 | ||||||
chr12:112445719
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-557G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445719 | ||||||
chr12:112445871
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.15-405C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445871 | ||||||
chr12:112445929
|
C | T | 1 | a0001c0001t0003g0131 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.15-347C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445929 | ||||||
chr12:112445978
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15-298C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112445978 | ||||||
chr12:112446074
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.15-202A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112446074 | ||||||
chr12:112446081
|
C | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG02622.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15-195C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 1/15 | chr12 | 112446081 | ||||||
chr12:112446740
|
AT | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0066a0001c0001t0001g0102others(6): Show | 9 | HG01167.hp1 HG02027.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+357delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112446740 | |||||
chr12:112447192
|
A | G | 6 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0260others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+794A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447192 | ||||||
chr12:112447349
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0002g0178 | 2 | NA18973.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.137+951C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447349 | ||||||
chr12:112447463
|
A | G | 6 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0260others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+1065A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447463 | ||||||
chr12:112447705
|
G | A | 74 | a0001c0001t0001g0064a0001c0001t0001g0211a0001c0001t0001g0250others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.137+1307G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447705 | ||||||
chr12:112447799
|
C | CT | 16 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0027others(13): Show | 16 | HG01952.hp2 HG02027.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.137+1420dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112447799 | |||||
chr12:112447835
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+1437C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112447835 | ||||||
chr12:112448175
|
C | G | 1 | a0003c0004t0003g0173 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.137+1777C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112448175 | ||||||
chr12:112449046
|
C | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1272C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449046 | ||||||
chr12:112449204
|
C | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(285): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.138-1114C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449204 | ||||||
chr12:112449211
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138-1107G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449211 | ||||||
chr12:112449240
|
C | T | 4 | a0001c0001t0001g0277a0001c0001t0007g0107a0001c0001t0007g0116others(1): Show | 4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-1078C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449240 | ||||||
chr12:112449333
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.138-985G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449333 | ||||||
chr12:112449371
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0200a0001c0001t0001g0202 | 4 | HG01099.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-947G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449371 | ||||||
chr12:112449497
|
ACT | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-818_138-817del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112449497 | |||||
chr12:112449756
|
T | A | 1 | a0001c0001t0003g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.138-562T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449756 | ||||||
chr12:112449925
|
C | T | 4 | a0001c0001t0001g0277a0001c0001t0007g0107a0001c0001t0007g0116others(1): Show | 4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-393C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449925 | ||||||
chr12:112449928
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.138-390G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449928 | ||||||
chr12:112449990
|
G | A | 2 | a0001c0001t0003g0132a0001c0001t0003g0155 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.138-328G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112449990 | ||||||
chr12:112450086
|
C | CA | 7 | a0001c0001t0001g0278a0001c0001t0005g0016a0001c0001t0005g0017others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-216dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 112450086 | |||||
chr12:112450137
|
G | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138-181G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450137 | ||||||
chr12:112450238
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138-80G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450238 | ||||||
chr12:112450241
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.138-77G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 2/15 | chr12 | 112450241 | ||||||
chr12:112450888
|
C | A | 10 | a0001c0001t0003g0112a0001c0001t0003g0140a0001c0001t0003g0165others(7): Show | 10 | HG00140.hp2 HG00738.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+376C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112450888 | ||||||
chr12:112451242
|
T | C | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332+730T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451242 | ||||||
chr12:112451320
|
T | A | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.332+808T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451320 | ||||||
chr12:112451511
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0046 | 2 | HG01943.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.332+999C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451511 | ||||||
chr12:112451851
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.332+1339C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451851 | ||||||
chr12:112451880
|
T | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.333-1315T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451880 | ||||||
chr12:112451936
|
C | T | 1 | a0001c0001t0005g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333-1259C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112451936 | ||||||
chr12:112452118
|
C | T | 4 | a0001c0001t0001g0211a0001c0001t0002g0212a0001c0001t0002g0216others(1): Show | 4 | HG02027.hp1 HG02135.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-1077C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452118 | ||||||
chr12:112452178
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-1017A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452178 | ||||||
chr12:112452263
|
G | A | 1 | a0001c0001t0013g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.333-932G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452263 | ||||||
chr12:112452601
|
C | T | 4 | a0001c0002t0001g0039a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.333-594C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452601 | ||||||
chr12:112452972
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 179 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.333-223A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 3/15 | chr12 | 112452972 | ||||||
chr12:112453465
|
A | G | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+78A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453465 | ||||||
chr12:112453488
|
T | TTTTA | 18 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(15): Show | 19 | HG01496.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+129_525+132dup others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112453488 | |||||
chr12:112453532
|
T | A | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.525+145T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453532 | ||||||
chr12:112453646
|
G | GT | 6 | a0001c0001t0001g0198a0001c0001t0001g0277a0001c0001t0002g0118others(3): Show | 6 | HG03098.hp2 HG03516.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+275dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112453646 | |||||
chr12:112453647
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.525+260T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453647 | ||||||
chr12:112453657
|
T | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0052 | 2 | HG01978.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.525+270T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453657 | ||||||
chr12:112453658
|
T | G | 3 | a0001c0001t0006g0135a0001c0001t0006g0205a0001c0001t0006g0207 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.525+271T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453658 | ||||||
chr12:112453659
|
T | G | 7 | a0001c0001t0001g0050a0001c0001t0004g0022a0001c0001t0004g0023others(4): Show | 7 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+272T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453659 | ||||||
chr12:112453723
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.525+336G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453723 | ||||||
chr12:112453764
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.525+377C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453764 | ||||||
chr12:112453778
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0191 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+391T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453778 | ||||||
chr12:112453925
|
G | A | 1 | a0001c0001t0002g0209 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.525+538G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112453925 | ||||||
chr12:112454203
|
T | C | 1 | a0001c0001t0007g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-361T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112454203 | ||||||
chr12:112454424
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526-140A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | chr12 | 112454424 | ||||||
chr12:112454528
|
TAAC | T | 3 | a0001c0001t0005g0018a0001c0001t0005g0020a0001c0001t0005g0021 | 3 | HG03453.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.526-33_526-31delCA others(1): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 112454528 | |||||
chr12:112454818
|
C | CT | 10 | a0001c0001t0001g0097a0001c0001t0001g0278a0001c0001t0002g0232others(7): Show | 10 | HG02148.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+159dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112454818 | |||||
chr12:112454818
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.642+138C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112454818 | ||||||
chr12:112454818
|
CT | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0067others(14): Show | 17 | HG01099.hp1 HG02273.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+159delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112454818 | |||||
chr12:112454922
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.642+242C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112454922 | ||||||
chr12:112455154
|
C | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.642+474C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455154 | ||||||
chr12:112455162
|
A | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.642+482A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455162 | ||||||
chr12:112455232
|
C | CT | 10 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0093others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.642+573dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455232 | |||||
chr12:112455352
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.643-598C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455352 | ||||||
chr12:112455688
|
C | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.643-262C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455688 | ||||||
chr12:112455792
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.643-158C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | chr12 | 112455792 | ||||||
chr12:112455871
|
G | GT | 17 | a0001c0001t0001g0061a0001c0001t0001g0091a0001c0001t0001g0100others(14): Show | 17 | HG00621.hp1 HG00621.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-62dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455871 | |||||
chr12:112455871
|
GT | G | 11 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0050others(8): Show | 11 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-62delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 112455871 | |||||
chr12:112456458
|
CT | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 170 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(167): Show |
intron_variant | MODIFIER | c.756+413delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112456458 | |||||
chr12:112456458
|
CTT | C | 6 | a0001c0001t0001g0026a0001c0001t0002g0227a0001c0001t0004g0022others(3): Show | 6 | HG01167.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.756+412_756+413del others(2): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112456458 | |||||
chr12:112456899
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.756+836G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112456899 | ||||||
chr12:112457163
|
C | G | 1 | a0001c0001t0002g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.756+1100C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457163 | ||||||
chr12:112457337
|
G | A | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.756+1274G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457337 | ||||||
chr12:112457407
|
C | T | 1 | a0001c0001t0011g0146 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756+1344C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457407 | ||||||
chr12:112457493
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.756+1430T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457493 | ||||||
chr12:112457878
|
A | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0282a0001c0001t0002g0285 | 3 | HG02080.hp1 NA18961.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.756+1815A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457878 | ||||||
chr12:112457908
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0087 | 4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+1845G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112457908 | ||||||
chr12:112459036
|
A | AG | 276 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(273): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.756+2973_756+2974i others(3): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459036 | ||||||
chr12:112459144
|
GCAGT | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0288others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+3084_756+3087d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459144 | |||||
chr12:112459326
|
T | C | 3 | a0001c0001t0006g0135a0001c0001t0006g0205a0001c0001t0006g0207 | 3 | HG01361.hp2 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.756+3263T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459326 | ||||||
chr12:112459365
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.756+3302A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459365 | ||||||
chr12:112459433
|
CT | C | 6 | a0001c0001t0001g0108a0001c0001t0002g0210a0001c0001t0002g0213others(3): Show | 6 | HG02976.hp1 NA18951.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+3385delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459433 | |||||
chr12:112459435
|
T | G | 1 | a0001c0001t0003g0122 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.756+3372T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459435 | ||||||
chr12:112459793
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0003g0137 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.756+3730T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459793 | ||||||
chr12:112459868
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.756+3805C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112459868 | ||||||
chr12:112459908
|
T | TAC | 40 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 41 | HG01258.hp1 HG01361.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.756+3878_756+3879d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | |||||
chr12:112459908
|
T | TACAC | 7 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG00099.hp1 HG01099.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.756+3876_756+3879d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | |||||
chr12:112459908
|
TAC | T | 15 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0072others(12): Show | 15 | HG00621.hp2 HG02165.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.756+3878_756+3879d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | |||||
chr12:112459908
|
TACAC | T | 45 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(42): Show | 45 | HG00140.hp1 HG00621.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.756+3876_756+3879d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112459908 | |||||
chr12:112460087
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.756+4024A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460087 | ||||||
chr12:112460175
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+4112C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460175 | ||||||
chr12:112460316
|
C | A | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.756+4253C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460316 | ||||||
chr12:112460482
|
T | G | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.756+4419T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460482 | ||||||
chr12:112460570
|
G | C | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+4507G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460570 | ||||||
chr12:112460660
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG01943.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+4597G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460660 | ||||||
chr12:112460710
|
T | C | 1 | a0001c0001t0011g0146 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.756+4647T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460710 | ||||||
chr12:112460874
|
T | G | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.756+4811T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112460874 | ||||||
chr12:112461292
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.756+5229G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461292 | ||||||
chr12:112461338
|
CT | C | 7 | a0001c0001t0002g0210a0001c0001t0005g0016a0001c0001t0005g0017others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.756+5289delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112461338 | |||||
chr12:112461433
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.756+5370C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461433 | ||||||
chr12:112461655
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.756+5592A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461655 | ||||||
chr12:112461676
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.756+5613C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112461676 | ||||||
chr12:112462528
|
T | C | 2 | a0001c0001t0003g0127a0001c0001t0016g0142 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.756+6465T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462528 | ||||||
chr12:112462906
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0004g0048a0001c0001t0018g0049 | 3 | HG02976.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.756+6843T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462906 | ||||||
chr12:112462978
|
C | G | 4 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0254others(1): Show | 4 | HG00735.hp1 HG01081.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+6915C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112462978 | ||||||
chr12:112463656
|
T | G | 1 | a0001c0001t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.756+7593T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463656 | ||||||
chr12:112463787
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.756+7724A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463787 | ||||||
chr12:112463877
|
G | C | 2 | a0001c0001t0005g0017a0001c0001t0005g0019 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.756+7814G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463877 | ||||||
chr12:112463911
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.756+7848C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112463911 | ||||||
chr12:112464236
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0191 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.756+8173C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464236 | ||||||
chr12:112464281
|
G | A | 2 | a0001c0002t0001g0034a0001c0002t0001g0176 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.756+8218G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464281 | ||||||
chr12:112464520
|
C | T | 24 | a0001c0001t0001g0250a0001c0001t0002g0001a0001c0001t0002g0005others(21): Show | 31 | HG00544.hp2 HG02071.hp1 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.757-8424C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112464520 | ||||||
chr12:112465004
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0111a0001c0001t0001g0276 | 3 | HG01109.hp2 HG02145.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.757-7940C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465004 | ||||||
chr12:112465129
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.757-7815G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465129 | ||||||
chr12:112465169
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-7775C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465169 | ||||||
chr12:112465193
|
A | G | 1 | a0001c0001t0018g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.757-7751A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465193 | ||||||
chr12:112465238
|
C | T | 1 | a0001c0001t0002g0251 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.757-7706C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465238 | ||||||
chr12:112465420
|
C | CA | 12 | a0001c0001t0001g0111a0001c0001t0001g0277a0001c0001t0002g0285others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.757-7508dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112465420 | |||||
chr12:112465473
|
T | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-7471T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465473 | ||||||
chr12:112465546
|
C | T | 1 | a0001c0001t0005g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.757-7398C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465546 | ||||||
chr12:112465595
|
A | G | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757-7349A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465595 | ||||||
chr12:112465989
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-6955G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112465989 | ||||||
chr12:112466010
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.757-6934C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466010 | ||||||
chr12:112466068
|
A | G | 1 | a0001c0001t0002g0225 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.757-6876A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466068 | ||||||
chr12:112466346
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.757-6598T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466346 | ||||||
chr12:112466427
|
A | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(70): Show | 75 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.757-6517A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466427 | ||||||
chr12:112466596
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0152 | 2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.757-6348C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466596 | ||||||
chr12:112466605
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-6339G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466605 | ||||||
chr12:112466666
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.757-6278A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466666 | ||||||
chr12:112466685
|
G | T | 1 | a0001c0001t0002g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.757-6259G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466685 | ||||||
chr12:112466773
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.757-6171A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466773 | ||||||
chr12:112466904
|
C | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02056.hp1 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-6040C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112466904 | ||||||
chr12:112466909
|
T | TGGTCCTT others(6): Show |
6 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02056.hp1 HG02071.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-6034_757-6022d others(15): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112466909 | |||||
chr12:112467118
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.757-5826A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467118 | ||||||
chr12:112467151
|
A | G | 5 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0265others(2): Show | 5 | HG01071.hp1 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-5793A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467151 | ||||||
chr12:112467167
|
C | A | 2 | a0001c0001t0001g0115a0001c0001t0003g0137 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.757-5777C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467167 | ||||||
chr12:112467467
|
A | G | 2 | a0001c0001t0003g0127a0001c0001t0016g0142 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.757-5477A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467467 | ||||||
chr12:112467486
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.757-5458G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467486 | ||||||
chr12:112467737
|
C | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(23): Show | 26 | HG00140.hp2 HG00738.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.757-5207C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467737 | ||||||
chr12:112467962
|
C | T | 3 | a0001c0001t0002g0233a0001c0001t0002g0282a0001c0001t0002g0285 | 3 | HG02080.hp1 NA18961.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.757-4982C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112467962 | ||||||
chr12:112468045
|
C | A | 5 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0108others(2): Show | 5 | NA18942.hp1 NA18960.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-4899C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468045 | ||||||
chr12:112468218
|
G | A | 2 | a0001c0001t0005g0017a0001c0001t0005g0019 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.757-4726G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468218 | ||||||
chr12:112468310
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.757-4634T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468310 | ||||||
chr12:112468611
|
A | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(268): Show | 281 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(278): Show |
intron_variant | MODIFIER | c.757-4333A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468611 | ||||||
chr12:112468648
|
G | T | 1 | a0001c0001t0002g0118 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.757-4296G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468648 | ||||||
chr12:112468728
|
C | A | 1 | a0001c0001t0002g0118 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.757-4216C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468728 | ||||||
chr12:112468835
|
C | G | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.757-4109C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468835 | ||||||
chr12:112468843
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0007g0107a0001c0001t0007g0116others(1): Show | 4 | HG03098.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-4101G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112468843 | ||||||
chr12:112469069
|
C | CA | 18 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0209others(15): Show | 25 | HG00544.hp2 HG02132.hp2 NA18941.hp1 others(22): Show |
intron_variant | MODIFIER | c.757-3866dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112469069 | |||||
chr12:112469178
|
A | C | 1 | a0001c0001t0002g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.757-3766A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469178 | ||||||
chr12:112469258
|
G | C | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.757-3686G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469258 | ||||||
chr12:112469572
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-3372T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469572 | ||||||
chr12:112469579
|
A | G | 1 | a0001c0001t0002g0290 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.757-3365A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112469579 | ||||||
chr12:112470147
|
C | T | 1 | a0002c0003t0003g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-2797C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470147 | ||||||
chr12:112470330
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.757-2614T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470330 | ||||||
chr12:112470899
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.757-2045C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112470899 | ||||||
chr12:112471125
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.757-1819G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471125 | ||||||
chr12:112471451
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.757-1493A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471451 | ||||||
chr12:112471452
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.757-1492G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471452 | ||||||
chr12:112471454
|
A | AAG | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(62): Show | 67 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.757-1454_757-1453d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
A | AAGAG | 37 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0104others(34): Show | 43 | HG00544.hp2 HG01099.hp1 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.757-1456_757-1453d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
A | AAGAGAG | 6 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0063others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-1458_757-1453d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
A | AAGAGAGA others(3): Show |
4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-1462_757-1453d others(12): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
A | AAGAGAGA others(5): Show |
1 | a0001c0001t0003g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.757-1464_757-1453d others(14): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.757-1490_757-1489i others(13): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471454 | ||||||
chr12:112471454
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0013g0175 | 2 | HG02572.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.757-1490A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471454 | ||||||
chr12:112471454
|
AAG | A | 14 | a0001c0001t0001g0106a0001c0001t0001g0201a0001c0001t0002g0226others(11): Show | 14 | HG01081.hp2 HG01934.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.757-1454_757-1453d others(4): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
AAGAG | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.757-1456_757-1453d others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471454
|
AAGAGAG | A | 5 | a0001c0001t0002g0246a0001c0001t0003g0123a0001c0002t0001g0035others(2): Show | 5 | HG02109.hp2 HG02683.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-1458_757-1453d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 112471454 | |||||
chr12:112471526
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-1418A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471526 | ||||||
chr12:112471536
|
T | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(66): Show | 71 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.757-1408T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471536 | ||||||
chr12:112471566
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.757-1378G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471566 | ||||||
chr12:112471592
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-1352T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471592 | ||||||
chr12:112471643
|
G | T | 1 | a0001c0001t0003g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.757-1301G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471643 | ||||||
chr12:112471713
|
G | T | 3 | a0001c0001t0001g0277a0001c0001t0007g0116a0001c0001t0007g0199 | 3 | HG03098.hp2 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.757-1231G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471713 | ||||||
chr12:112471918
|
A | G | 3 | a0001c0002t0001g0035a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | HG02109.hp2 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.757-1026A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112471918 | ||||||
chr12:112472306
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.757-638A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472306 | ||||||
chr12:112472415
|
G | A | 2 | a0001c0001t0006g0206a0001c0001t0006g0208 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.757-529G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472415 | ||||||
chr12:112472463
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.757-481G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472463 | ||||||
chr12:112472565
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG00621.hp1 NA18959.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.757-379G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472565 | ||||||
chr12:112472576
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.757-368C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472576 | ||||||
chr12:112472720
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.757-224C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472720 | ||||||
chr12:112472875
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0087 | 4 | HG01167.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.757-69T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 6/15 | chr12 | 112472875 | ||||||
chr12:112473356
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.853+316T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473356 | ||||||
chr12:112473419
|
C | T | 1 | a0001c0001t0006g0207 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853+379C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473419 | ||||||
chr12:112473509
|
G | C | 2 | a0001c0002t0001g0034a0001c0002t0001g0176 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.853+469G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473509 | ||||||
chr12:112473635
|
T | TC | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.853+596dupC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112473635 | |||||
chr12:112473720
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.853+680G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473720 | ||||||
chr12:112473821
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+781G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473821 | ||||||
chr12:112473845
|
C | CA | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 22 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.853+817dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112473845 | |||||
chr12:112473978
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.853+938G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112473978 | ||||||
chr12:112474287
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.853+1247C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474287 | ||||||
chr12:112474389
|
T | A | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.853+1349T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474389 | ||||||
chr12:112474393
|
A | T | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.853+1353A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474393 | ||||||
chr12:112474728
|
A | G | 2 | a0001c0001t0007g0116a0001c0001t0007g0199 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.853+1688A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112474728 | ||||||
chr12:112475063
|
C | T | 2 | a0001c0001t0003g0127a0001c0001t0016g0142 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.853+2023C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475063 | ||||||
chr12:112475246
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.853+2206C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475246 | ||||||
chr12:112475441
|
T | TG | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 13 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.854-2204dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 112475441 | |||||
chr12:112475528
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0003g0137 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.854-2123T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475528 | ||||||
chr12:112475988
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.854-1663T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112475988 | ||||||
chr12:112476030
|
C | T | 1 | a0001c0001t0005g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.854-1621C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476030 | ||||||
chr12:112476038
|
C | A | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1613C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476038 | ||||||
chr12:112476248
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.854-1403A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476248 | ||||||
chr12:112476397
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.854-1254G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476397 | ||||||
chr12:112476419
|
A | T | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1232A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476419 | ||||||
chr12:112476527
|
G | A | 74 | a0001c0001t0001g0211a0001c0001t0001g0250a0001c0001t0002g0001others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.854-1124G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476527 | ||||||
chr12:112476541
|
G | T | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.854-1110G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476541 | ||||||
chr12:112476864
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.854-787T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112476864 | ||||||
chr12:112477047
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.854-604G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477047 | ||||||
chr12:112477103
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.854-548G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477103 | ||||||
chr12:112477120
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-531G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477120 | ||||||
chr12:112477172
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.854-479A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477172 | ||||||
chr12:112477362
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.854-289T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477362 | ||||||
chr12:112477428
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.854-223C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477428 | ||||||
chr12:112477494
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.854-157C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477494 | ||||||
chr12:112477619
|
A | C | 7 | a0001c0001t0002g0041a0001c0001t0002g0268a0001c0001t0002g0269others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-32A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477619 | ||||||
chr12:112477621
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0265 | 3 | HG01496.hp1 HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.854-30T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477621 | ||||||
chr12:112477630
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0006g0135a0001c0001t0006g0205others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-21C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 7/15 | chr12 | 112477630 | ||||||
chr12:112478400
|
C | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1092+385C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478400 | ||||||
chr12:112478444
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0003g0147 | 2 | NA19058.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1092+429A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478444 | ||||||
chr12:112478532
|
G | A | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1092+517G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478532 | ||||||
chr12:112478716
|
G | A | 1 | a0001c0001t0003g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1092+701G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478716 | ||||||
chr12:112478879
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0006g0135a0001c0001t0006g0205others(3): Show | 6 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092+864C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478879 | ||||||
chr12:112478981
|
T | G | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 23 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1092+966T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112478981 | ||||||
chr12:112479009
|
T | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 23 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1092+994T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479009 | ||||||
chr12:112479345
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1092+1330A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479345 | ||||||
chr12:112479559
|
T | C | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1092+1544T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479559 | ||||||
chr12:112479863
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0174 | 2 | HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1092+1848T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112479863 | ||||||
chr12:112480084
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1093-1990C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480084 | ||||||
chr12:112480107
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-1967G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480107 | ||||||
chr12:112480366
|
C | CT | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(73): Show | 78 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1093-1690dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480366 | |||||
chr12:112480366
|
CT | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0145others(16): Show | 19 | HG00099.hp2 HG01099.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1093-1690delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480366 | |||||
chr12:112480422
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1093-1652A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480422 | ||||||
chr12:112480448
|
G | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 183 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(180): Show |
intron_variant | MODIFIER | c.1093-1626G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480448 | ||||||
chr12:112480460
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1093-1614G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480460 | ||||||
chr12:112480486
|
T | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(170): Show | 183 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(180): Show |
intron_variant | MODIFIER | c.1093-1588T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480486 | ||||||
chr12:112480555
|
A | AG | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 254 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(251): Show |
intron_variant | MODIFIER | c.1093-1517dupG | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 112480555 | |||||
chr12:112480611
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1093-1463C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480611 | ||||||
chr12:112480652
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0010 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1093-1422G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480652 | ||||||
chr12:112480687
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1093-1387C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480687 | ||||||
chr12:112480847
|
G | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1093-1227G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480847 | ||||||
chr12:112480915
|
A | C | 1 | a0001c0001t0002g0235 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1093-1159A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112480915 | ||||||
chr12:112481744
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1093-330G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112481744 | ||||||
chr12:112482065
|
C | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1093-9C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 9/15 | chr12 | 112482065 | ||||||
chr12:112482463
|
C | T | 9 | a0001c0001t0002g0041a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG01071.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224+258C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482463 | ||||||
chr12:112482602
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1224+397C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482602 | ||||||
chr12:112482797
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1224+592A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112482797 | ||||||
chr12:112483042
|
A | G | 1 | a0001c0001t0010g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1224+837A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483042 | ||||||
chr12:112483098
|
T | C | 1 | a0001c0001t0002g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1224+893T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483098 | ||||||
chr12:112483687
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1224+1482C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483687 | ||||||
chr12:112483831
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1224+1626C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483831 | ||||||
chr12:112483857
|
T | C | 1 | a0001c0001t0003g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1224+1652T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483857 | ||||||
chr12:112483893
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1224+1688G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483893 | ||||||
chr12:112483931
|
T | C | 1 | a0001c0001t0003g0122 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1224+1726T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483931 | ||||||
chr12:112483933
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1224+1728C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112483933 | ||||||
chr12:112484096
|
C | T | 1 | a0001c0001t0007g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1224+1891C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484096 | ||||||
chr12:112484235
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1224+2030A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484235 | ||||||
chr12:112484286
|
G | A | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1224+2081G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484286 | ||||||
chr12:112484533
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(71): Show | 76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.1225-1942C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484533 | ||||||
chr12:112484725
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 211 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(208): Show |
intron_variant | MODIFIER | c.1225-1750G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484725 | ||||||
chr12:112484775
|
A | C | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1225-1700A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484775 | ||||||
chr12:112484923
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1225-1552G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112484923 | ||||||
chr12:112485032
|
G | T | 1 | a0001c0001t0014g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1225-1443G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485032 | ||||||
chr12:112485177
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1225-1298C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485177 | ||||||
chr12:112485334
|
C | T | 1 | a0001c0001t0022g0279 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1225-1141C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485334 | ||||||
chr12:112485557
|
G | A | 28 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0043others(25): Show | 28 | HG00099.hp2 HG01099.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1225-918G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485557 | ||||||
chr12:112485588
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1225-887C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485588 | ||||||
chr12:112485589
|
G | A | 42 | a0001c0001t0001g0250a0001c0001t0002g0001a0001c0001t0002g0005others(39): Show | 49 | HG00544.hp2 HG02027.hp1 HG02071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1225-886G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485589 | ||||||
chr12:112485887
|
A | C | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225-588A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112485887 | ||||||
chr12:112485982
|
GA | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(9): Show | 13 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1225-477delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 112485982 | |||||
chr12:112486010
|
T | TAATAAA | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(202): Show | 215 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(212): Show |
intron_variant | MODIFIER | c.1225-464_1225-463i others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 112486010 | |||||
chr12:112486412
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1225-63G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112486412 | ||||||
chr12:112486425
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1225-50A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 10/15 | chr12 | 112486425 | ||||||
chr12:112486649
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0275 | 2 | NA18954.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1379+20C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486649 | ||||||
chr12:112486902
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1379+273G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486902 | ||||||
chr12:112486937
|
C | T | 2 | a0001c0002t0001g0162a0001c0002t0001g0163 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1379+308C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486937 | ||||||
chr12:112486999
|
G | T | 1 | a0001c0001t0005g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1379+370G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112486999 | ||||||
chr12:112487023
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0109a0001c0001t0001g0139 | 3 | NA18971.hp1 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1379+394T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487023 | ||||||
chr12:112487115
|
TTCTCTC | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1379+500_1379+505d others(8): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 112487115 | |||||
chr12:112487116
|
TC | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0117 | 3 | HG02132.hp1 HG02523.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1379+488delC | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487116 | ||||||
chr12:112487135
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 7 | HG01081.hp2 HG01099.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1379+506T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487135 | ||||||
chr12:112487718
|
A | G | 2 | a0001c0001t0004g0048a0001c0001t0018g0049 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1380-725A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 11/15 | chr12 | 112487718 | ||||||
chr12:112488661
|
C | T | 1 | a0001c0001t0003g0073 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1447+151C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 12/15 | chr12 | 112488661 | ||||||
chr12:112488968
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1448-56C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 12/15 | chr12 | 112488968 | ||||||
chr12:112489407
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0010g0153 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1599+232C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489407 | ||||||
chr12:112489468
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+293C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489468 | ||||||
chr12:112489549
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1599+374C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489549 | ||||||
chr12:112489560
|
C | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 9 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1599+385C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489560 | ||||||
chr12:112489605
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1599+430G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489605 | ||||||
chr12:112489668
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+493C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112489668 | ||||||
chr12:112490241
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1066C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490241 | ||||||
chr12:112490297
|
G | C | 4 | a0001c0002t0001g0039a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1122G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490297 | ||||||
chr12:112490304
|
C | CT | 82 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0080others(79): Show | 89 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.1599+1148dupT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112490304 | |||||
chr12:112490393
|
A | G | 4 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0001t0003g0157others(1): Show | 4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+1218A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490393 | ||||||
chr12:112490503
|
C | T | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599+1328C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490503 | ||||||
chr12:112490594
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1599+1419C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490594 | ||||||
chr12:112490601
|
C | T | 2 | a0001c0001t0004g0048a0001c0001t0018g0049 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1599+1426C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490601 | ||||||
chr12:112490603
|
C | T | 2 | a0001c0001t0004g0286a0001c0001t0022g0279 | 2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1599+1428C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490603 | ||||||
chr12:112490647
|
G | A | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(200): Show | 213 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(210): Show |
intron_variant | MODIFIER | c.1599+1472G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490647 | ||||||
chr12:112490792
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1599+1617A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112490792 | ||||||
chr12:112491272
|
G | GA | 74 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0158others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.1599+2112dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112491272 | |||||
chr12:112491903
|
C | T | 3 | a0001c0001t0003g0073a0001c0001t0003g0120a0001c0001t0003g0121 | 3 | NA18984.hp2 NA18986.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1599+2728C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112491903 | ||||||
chr12:112492068
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1599+2893A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492068 | ||||||
chr12:112492476
|
G | T | 18 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0096others(15): Show | 18 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1599+3301G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492476 | ||||||
chr12:112492539
|
A | T | 1 | a0001c0001t0005g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1599+3364A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492539 | ||||||
chr12:112492604
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1599+3429A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492604 | ||||||
chr12:112492610
|
C | T | 1 | a0001c0001t0005g0016 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1599+3435C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492610 | ||||||
chr12:112492611
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1599+3436G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492611 | ||||||
chr12:112492616
|
G | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG01943.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1599+3441G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492616 | ||||||
chr12:112492671
|
T | C | 17 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0118others(14): Show | 24 | HG00544.hp2 HG02132.hp2 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1599+3496T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492671 | ||||||
chr12:112492713
|
C | T | 10 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0001t0002g0260others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1599+3538C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492713 | ||||||
chr12:112492724
|
A | G | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+3549A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492724 | ||||||
chr12:112492737
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 24 | HG01081.hp2 HG01099.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1599+3562T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492737 | ||||||
chr12:112492752
|
T | C | 1 | a0001c0001t0004g0286 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1599+3577T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492752 | ||||||
chr12:112492812
|
C | T | 1 | a0001c0001t0002g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1599+3637C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492812 | ||||||
chr12:112492856
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0275 | 2 | NA18954.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1599+3681T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492856 | ||||||
chr12:112492975
|
A | G | 2 | a0001c0001t0002g0248a0001c0001t0019g0249 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1599+3800A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492975 | ||||||
chr12:112492986
|
T | C | 4 | a0001c0002t0001g0039a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG02965.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+3811T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112492986 | ||||||
chr12:112493074
|
T | C | 1 | a0001c0001t0002g0287 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1599+3899T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493074 | ||||||
chr12:112493220
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1599+4045G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493220 | ||||||
chr12:112493383
|
AT | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 17 | HG01256.hp1 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1599+4227delT | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112493383 | |||||
chr12:112493479
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1599+4304G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493479 | ||||||
chr12:112493559
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0096others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+4384T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493559 | ||||||
chr12:112493871
|
T | A | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1599+4696T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112493871 | ||||||
chr12:112494030
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1599+4855A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494030 | ||||||
chr12:112494444
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1599+5269A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494444 | ||||||
chr12:112494476
|
GTTA | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+5304_1599+530 others(7): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112494476 | |||||
chr12:112494867
|
C | T | 2 | a0001c0001t0008g0234a0001c0001t0020g0238 | 2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1599+5692C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112494867 | ||||||
chr12:112495023
|
T | G | 16 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(13): Show | 16 | HG01993.hp2 HG02135.hp2 HG03710.hp2 others(13): Show |
intron_variant | MODIFIER | c.1599+5848T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495023 | ||||||
chr12:112495029
|
A | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG02055.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1599+5854A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495029 | ||||||
chr12:112495242
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG02055.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1599+6067A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495242 | ||||||
chr12:112495573
|
A | G | 1 | a0001c0001t0003g0264 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1599+6398A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495573 | ||||||
chr12:112495731
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(166): Show | 179 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.1600-6413G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495731 | ||||||
chr12:112495898
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1600-6246A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495898 | ||||||
chr12:112495988
|
C | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-6156C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112495988 | ||||||
chr12:112496116
|
A | G | 3 | a0001c0001t0007g0107a0001c0001t0007g0116a0001c0001t0007g0199 | 3 | HG03516.hp1 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1600-6028A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496116 | ||||||
chr12:112496526
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00621.hp2 NA18945.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1600-5618T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496526 | ||||||
chr12:112496810
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1600-5334C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496810 | ||||||
chr12:112496905
|
G | C | 1 | a0001c0001t0014g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1600-5239G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112496905 | ||||||
chr12:112497159
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0004g0033 | 3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1600-4985G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497159 | ||||||
chr12:112497171
|
C | CA | 13 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0076others(10): Show | 13 | HG01361.hp2 HG02109.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1600-4952dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | |||||
chr12:112497171
|
CA | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(107): Show | 119 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1600-4952delA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | |||||
chr12:112497171
|
CAA | C | 8 | a0001c0001t0002g0246a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1600-4953_1600-495 others(6): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112497171 | |||||
chr12:112497260
|
G | A | 6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-4884G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497260 | ||||||
chr12:112497414
|
T | A | 1 | a0001c0001t0002g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1600-4730T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497414 | ||||||
chr12:112497540
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(71): Show | 76 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(73): Show |
intron_variant | MODIFIER | c.1600-4604C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497540 | ||||||
chr12:112497568
|
A | G | 1 | a0001c0001t0012g0222 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1600-4576A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497568 | ||||||
chr12:112497696
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1600-4448G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497696 | ||||||
chr12:112497749
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 182 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(179): Show |
intron_variant | MODIFIER | c.1600-4395C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497749 | ||||||
chr12:112497793
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-4351G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497793 | ||||||
chr12:112497793
|
G | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-4351G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497793 | ||||||
chr12:112497962
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1600-4182G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112497962 | ||||||
chr12:112498152
|
C | CA | 74 | a0001c0001t0001g0061a0001c0001t0002g0001a0001c0001t0002g0005others(71): Show | 81 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.1600-3982dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112498152 | |||||
chr12:112498161
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1600-3983A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498161 | ||||||
chr12:112498270
|
C | T | 1 | a0001c0001t0014g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1600-3874C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498270 | ||||||
chr12:112498326
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | NA18952.hp2 NA18973.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1600-3818C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498326 | ||||||
chr12:112498463
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1600-3681C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112498463 | ||||||
chr12:112499114
|
ATCT | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-3026_1600-302 others(7): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112499114 | |||||
chr12:112499327
|
T | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1600-2817T>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499327 | ||||||
chr12:112499430
|
C | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-2714C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499430 | ||||||
chr12:112499496
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1600-2648C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499496 | ||||||
chr12:112499552
|
T | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1600-2592T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499552 | ||||||
chr12:112499623
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1600-2521G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112499623 | ||||||
chr12:112499943
|
T | TA | 8 | a0001c0001t0001g0080a0001c0001t0002g0214a0001c0001t0002g0255others(5): Show | 8 | HG01891.hp2 HG02074.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1600-2183dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112499943 | |||||
chr12:112500182
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 12 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-1962A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500182 | ||||||
chr12:112500338
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1600-1806T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500338 | ||||||
chr12:112500402
|
A | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0176 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1600-1742A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500402 | ||||||
chr12:112500484
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1600-1660C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500484 | ||||||
chr12:112500565
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-1579G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500565 | ||||||
chr12:112500657
|
T | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0145a0001c0001t0001g0288others(9): Show | 12 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-1487T>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500657 | ||||||
chr12:112500920
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1600-1224C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500920 | ||||||
chr12:112500951
|
CCAGAGTG | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(67): Show | 72 | HG00621.hp1 HG00621.hp2 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.1600-1189_1600-118 others(11): Show |
PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 112500951 | |||||
chr12:112500999
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0096a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-1145G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112500999 | ||||||
chr12:112501286
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1600-858G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501286 | ||||||
chr12:112501557
|
G | A | 2 | a0001c0001t0004g0048a0001c0001t0018g0049 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-587G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501557 | ||||||
chr12:112501573
|
C | T | 2 | a0001c0001t0004g0048a0001c0001t0018g0049 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-571C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501573 | ||||||
chr12:112501727
|
T | C | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1600-417T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501727 | ||||||
chr12:112501759
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1600-385C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501759 | ||||||
chr12:112501814
|
A | T | 1 | a0001c0001t0003g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1600-330A>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501814 | ||||||
chr12:112501992
|
C | G | 1 | a0001c0001t0009g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1600-152C>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112501992 | ||||||
chr12:112502049
|
C | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(202): Show | 215 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(212): Show |
intron_variant | MODIFIER | c.1600-95C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 13/15 | chr12 | 112502049 | ||||||
chr12:112502303
|
A | G | 1 | a0001c0001t0014g0141 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1712+47A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502303 | ||||||
chr12:112502345
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1712+89G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502345 | ||||||
chr12:112502545
|
G | C | 2 | a0001c0001t0004g0048a0001c0001t0018g0049 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1712+289G>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502545 | ||||||
chr12:112502655
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1712+399G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502655 | ||||||
chr12:112502891
|
G | T | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG02109.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1712+635G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112502891 | ||||||
chr12:112503027
|
C | T | 1 | a0001c0001t0021g0143 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1712+771C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503027 | ||||||
chr12:112503243
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1712+987G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503243 | ||||||
chr12:112503322
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1712+1066A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503322 | ||||||
chr12:112503351
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 9 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1712+1095C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503351 | ||||||
chr12:112503368
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1712+1112T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503368 | ||||||
chr12:112503464
|
G | A | 1 | a0001c0001t0018g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1712+1208G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503464 | ||||||
chr12:112503550
|
C | A | 73 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0040others(70): Show | 80 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.1713-1145C>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503550 | ||||||
chr12:112503572
|
C | T | 1 | a0001c0001t0003g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1713-1123C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503572 | ||||||
chr12:112503627
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1713-1068A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503627 | ||||||
chr12:112503767
|
G | A | 232 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 242 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(239): Show |
intron_variant | MODIFIER | c.1713-928G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503767 | ||||||
chr12:112503946
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1713-749T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112503946 | ||||||
chr12:112504325
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1713-370A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504325 | ||||||
chr12:112504368
|
G | T | 1 | a0001c0001t0002g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1713-327G>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504368 | ||||||
chr12:112504549
|
G | A | 73 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0040others(70): Show | 80 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(77): Show |
intron_variant | MODIFIER | c.1713-146G>A | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 14/15 | chr12 | 112504549 | ||||||
chr12:112504942
|
T | C | 1 | a0001c0001t0003g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.*32+146T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112504942 | ||||||
chr12:112505063
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0174a0001c0001t0003g0078 | 3 | HG03654.hp1 HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.*32+267C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505063 | ||||||
chr12:112505393
|
A | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 242 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(239): Show |
intron_variant | MODIFIER | c.*33-432A>G | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505393 | ||||||
chr12:112505464
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0096a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.*33-361C>T | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505464 | ||||||
chr12:112505536
|
T | C | 5 | a0001c0001t0006g0135a0001c0001t0006g0205a0001c0001t0006g0206others(2): Show | 5 | HG00099.hp2 HG01099.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.*33-289T>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505536 | ||||||
chr12:112505656
|
C | CA | 40 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0043others(37): Show | 40 | HG00735.hp2 HG00738.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.*33-144dupA | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 112505656 | |||||
chr12:112505673
|
A | C | 8 | a0001c0001t0001g0115a0001c0001t0003g0137a0001c0001t0005g0016others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.*33-152A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505673 | ||||||
chr12:112505674
|
A | C | 71 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0040others(68): Show | 78 | HG00544.hp2 HG00735.hp1 HG01071.hp2 others(75): Show |
intron_variant | MODIFIER | c.*33-151A>C | PTPN11 | ENSG00000179295.19 | transcript | ENST00000351677.7 | protein_coding | 15/15 | chr12 | 112505674 |