geneid | 10254 |
---|---|
ensemblid | ENSG00000115145.10 |
hgncid | 11358 |
symbol | STAM2 |
name | signal transducing adaptor molecule 2 |
refseq_nuc | NM_005843.6 |
refseq_prot | NP_005834.4 |
ensembl_nuc | ENST00000263904.5 |
ensembl_prot | ENSP00000263904.4 |
mane_status | MANE Select |
chr | chr2 |
start | 152116801 |
end | 152175763 |
strand | - |
ver | v1.2 |
region | chr2:152116801-152175763 |
region5000 | chr2:152111801-152180763 |
regionname0 | STAM2_chr2_152116801_152175763 |
regionname5000 | STAM2_chr2_152111801_152180763 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 525 | 358 | 90 | 64 | 144 | 14 | 44 | 112 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0002 | 0/0 | 525 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1578 | 354 | 86 | 64 | 144 | 14 | 44 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
c0002 | 0/0 | 1578 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
c0003 | 0/0 | 1578 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
c0004 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3895 | 62 | 6 | 22 | 21 | 5 | 7 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0002 | 0/0 | 3894 | 41 | 1 | 0 | 29 | 0 | 11 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0003 | 0/1 | 3900 | 34 | 2 | 4 | 16 | 1 | 10 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0004 | 0/0 | 3898 | 27 | 3 | 10 | 12 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0005 | 0/0 | 3893 | 21 | 0 | 1 | 18 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0006 | 0/0 | 3894 | 21 | 5 | 7 | 5 | 3 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0007 | 0/0 | 3895 | 14 | 14 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0008 | 0/0 | 3895 | 13 | 1 | 3 | 7 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0009 | 0/0 | 3895 | 10 | 9 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0010 | 0/0 | 3895 | 7 | 0 | 0 | 7 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0011 | 0/0 | 3894 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0012 | 0/0 | 3897 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0013 | 0/0 | 3895 | 6 | 0 | 4 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0014 | 0/0 | 3898 | 6 | 5 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0015 | 0/0 | 3896 | 6 | 3 | 0 | 1 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0016 | 0/0 | 3895 | 5 | 5 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0017 | 0/0 | 3896 | 5 | 0 | 0 | 5 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0018 | 0/0 | 3898 | 4 | 4 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0019 | 0/0 | 3901 | 4 | 4 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0020 | 0/0 | 3903 | 4 | 3 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0021 | 0/0 | 3901 | 4 | 0 | 0 | 3 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0022 | 0/0 | 3897 | 4 | 0 | 3 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0023 | 0/0 | 3897 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0024 | 0/0 | 3902 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0025 | 0/0 | 3896 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0026 | 0/0 | 3895 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0027 | 0/0 | 3899 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0028 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0029 | 0/0 | 3894 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0030 | 0/0 | 3893 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0031 | 0/0 | 3893 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0032 | 0/0 | 3894 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0033 | 0/0 | 3894 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0034 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0035 | 0/0 | 3894 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0036 | 0/0 | 3894 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0037 | 0/0 | 3898 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0038 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0039 | 0/0 | 3898 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0040 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0041 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0042 | 0/0 | 3895 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0043 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0044 | 0/0 | 3899 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0045 | 0/0 | 3899 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0046 | 0/0 | 3896 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0047 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0048 | 0/0 | 3898 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0049 | 0/0 | 3900 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0050 | 0/0 | 3894 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0051 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0052 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0053 | 0/0 | 3897 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0054 | 0/0 | 3899 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0055 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0056 | 0/0 | 3898 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0057 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0058 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0059 | 0/0 | 3898 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0060 | 0/0 | 3894 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0061 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0062 | 0/0 | 3896 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
t0063 | 0/0 | 3894 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1578 | 354 | 86 | 64 | 144 | 14 | 44 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0002 | 0/0 | 1578 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0004 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0002c0003 | 0/0 | 1578 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5472 | 61 | 6 | 22 | 20 | 5 | 7 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0002 | 0/0 | 5471 | 41 | 1 | 0 | 29 | 0 | 11 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0003 | 0/1 | 5477 | 33 | 2 | 4 | 15 | 1 | 10 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0004 | 0/0 | 5475 | 27 | 3 | 10 | 12 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0005 | 0/0 | 5470 | 21 | 0 | 1 | 18 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0006 | 0/0 | 5471 | 21 | 5 | 7 | 5 | 3 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0007 | 0/0 | 5472 | 14 | 14 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0008 | 0/0 | 5472 | 13 | 1 | 3 | 7 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0009 | 0/0 | 5472 | 10 | 9 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0010 | 0/0 | 5472 | 7 | 0 | 0 | 7 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0011 | 0/0 | 5471 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0012 | 0/0 | 5474 | 7 | 6 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0013 | 0/0 | 5472 | 6 | 0 | 4 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0014 | 0/0 | 5475 | 6 | 5 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0015 | 0/0 | 5473 | 6 | 3 | 0 | 1 | 1 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0016 | 0/0 | 5472 | 5 | 5 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0017 | 0/0 | 5473 | 5 | 0 | 0 | 5 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0019 | 0/0 | 5478 | 4 | 4 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0020 | 0/0 | 5480 | 4 | 3 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0021 | 0/0 | 5478 | 4 | 0 | 0 | 3 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0022 | 0/0 | 5474 | 4 | 0 | 3 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0023 | 0/0 | 5474 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0024 | 0/0 | 5479 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0025 | 0/0 | 5473 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0026 | 0/0 | 5472 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0027 | 0/0 | 5476 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0028 | 0/0 | 5472 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0029 | 0/0 | 5471 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0030 | 0/0 | 5470 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0031 | 0/0 | 5470 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0032 | 0/0 | 5471 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0033 | 0/0 | 5471 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0034 | 0/0 | 5474 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0035 | 0/0 | 5471 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0036 | 0/0 | 5471 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0037 | 0/0 | 5475 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0038 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0039 | 0/0 | 5475 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0040 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0041 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0042 | 0/0 | 5472 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0043 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0044 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0045 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0046 | 0/0 | 5473 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0047 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0048 | 0/0 | 5475 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0049 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0050 | 0/0 | 5471 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0051 | 0/0 | 5472 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0052 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0053 | 0/0 | 5474 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0054 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0055 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0056 | 0/0 | 5475 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0057 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0058 | 0/0 | 5473 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0059 | 0/0 | 5475 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0060 | 0/0 | 5471 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0061 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0062 | 0/0 | 5473 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0001t0063 | 0/0 | 5471 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0002t0018 | 0/0 | 5475 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0001c0004t0018 | 0/0 | 5475 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0002c0003t0001 | 0/0 | 5472 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
a0002c0003t0003 | 0/0 | 5477 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | copy fasta | chr2 | 152111801 | 152180763 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0006g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0013g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0013g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0013g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0013g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0014g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0015g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0016g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0016g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0016g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0017g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0017g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0017g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0019g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0019g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0020g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0020g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0020g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0021g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0021g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0021g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0021g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0022g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0022g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0022g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0022g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0023g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0023g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0024g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0024g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0024g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0025g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0025g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0026g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0027g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0027g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0028g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0029g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0030g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0031g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0033g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0034g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0036g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0037g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0038g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0039g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0040g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0041g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0042g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0043g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0044g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0045g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0046g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0047g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0048g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0049g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0050g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0051g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0052g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0053g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0054g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0055g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0056g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0057g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0058g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0059g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0060g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0061g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0062g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0001t0063g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0002t0018g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0002t0018g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0002t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0001c0004t0018g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0219 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0177 | EUR | GBR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00280 | hp1 | a0001 | c0001 | t0032 | g0105 | EUR | FIN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00280 | hp2 | a0001 | c0001 | t0015 | g0288 | EUR | FIN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00408 | hp2 | a0001 | c0001 | t0017 | g0221 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00609 | hp1 | a0001 | c0001 | t0021 | g0234 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00639 | hp2 | a0001 | c0001 | t0020 | g0171 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0286 | EAS | CHS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0217 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01070 | hp1 | a0001 | c0001 | t0034 | g0200 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01070 | hp2 | a0001 | c0001 | t0027 | g0164 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0298 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0309 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0306 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0310 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01109 | hp2 | a0001 | c0001 | t0059 | g0189 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0137 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0036 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01192 | hp1 | a0001 | c0001 | t0013 | g0255 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0143 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01256 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01256 | hp2 | a0001 | c0001 | t0022 | g0212 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0025 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0311 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01496 | hp2 | a0001 | c0001 | t0027 | g0160 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0150 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01517 | hp1 | a0001 | c0001 | t0046 | g0246 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0149 | EUR | IBS | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01891 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01978 | hp1 | a0001 | c0001 | t0048 | g0201 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01981 | hp2 | a0001 | c0001 | t0022 | g0194 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02015 | hp1 | a0002 | c0003 | t0003 | g0229 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02027 | hp1 | a0001 | c0001 | t0040 | g0094 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02027 | hp2 | a0001 | c0001 | t0060 | g0307 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02040 | hp1 | a0001 | c0001 | t0023 | g0192 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02040 | hp2 | a0001 | c0001 | t0043 | g0289 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0290 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02055 | hp2 | a0001 | c0001 | t0015 | g0113 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0218 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02080 | hp1 | a0001 | c0001 | t0041 | g0284 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02145 | hp2 | a0001 | c0001 | t0050 | g0182 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02148 | hp2 | a0001 | c0001 | t0022 | g0207 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02165 | hp1 | a0001 | c0001 | t0021 | g0232 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02165 | hp2 | a0001 | c0001 | t0036 | g0088 | EAS | CDX | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02257 | hp1 | a0001 | c0001 | t0033 | g0111 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0174 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02258 | hp1 | a0001 | c0001 | t0019 | g0157 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0124 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0147 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02300 | hp1 | a0001 | c0001 | t0029 | g0138 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0167 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02622 | hp1 | a0001 | c0001 | t0044 | g0163 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0029 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02630 | hp1 | a0001 | c0001 | t0020 | g0170 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02647 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02647 | hp2 | a0001 | c0001 | t0053 | g0097 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02683 | hp1 | a0001 | c0001 | t0013 | g0293 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0162 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02738 | hp2 | a0001 | c0001 | t0021 | g0245 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0144 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02886 | hp1 | a0001 | c0001 | t0056 | g0154 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0165 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0303 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0166 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02922 | hp1 | a0001 | c0001 | t0058 | g0049 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0300 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0142 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02976 | hp1 | a0001 | c0004 | t0018 | g0176 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03041 | hp1 | a0001 | c0001 | t0054 | g0098 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0161 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03130 | hp1 | a0001 | c0001 | t0020 | g0173 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03139 | hp2 | a0001 | c0001 | t0045 | g0159 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03195 | hp1 | a0001 | c0001 | t0047 | g0178 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03195 | hp2 | a0001 | c0002 | t0018 | g0153 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03209 | hp1 | a0001 | c0001 | t0019 | g0158 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03225 | hp1 | a0001 | c0001 | t0016 | g0108 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0120 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03239 | hp2 | a0001 | c0001 | t0026 | g0021 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03540 | hp1 | a0001 | c0002 | t0018 | g0155 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03688 | hp1 | a0001 | c0001 | t0062 | g0315 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0294 | SAS | PJL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0314 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03834 | hp1 | a0001 | c0001 | t0037 | g0077 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0193 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03927 | hp2 | a0001 | c0001 | t0035 | g0064 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04115 | hp2 | a0001 | c0001 | t0015 | g0278 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04184 | hp1 | a0001 | c0001 | t0009 | g0030 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04228 | hp1 | a0001 | c0001 | t0026 | g0021 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0168 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0272 | EAS | CHB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0107 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18941 | hp1 | a0001 | c0001 | t0061 | g0317 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18942 | hp2 | a0001 | c0001 | t0008 | g0308 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18950 | hp2 | a0001 | c0001 | t0024 | g0191 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18952 | hp1 | a0001 | c0001 | t0024 | g0227 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18952 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18963 | hp1 | a0001 | c0001 | t0023 | g0196 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18968 | hp1 | a0001 | c0001 | t0008 | g0312 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18968 | hp2 | a0001 | c0001 | t0021 | g0243 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0320 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18970 | hp2 | a0001 | c0001 | t0063 | g0130 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18973 | hp1 | a0001 | c0001 | t0024 | g0235 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18982 | hp1 | a0001 | c0001 | t0010 | g0084 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18983 | hp1 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18986 | hp1 | a0001 | c0001 | t0052 | g0083 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18986 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18994 | hp1 | a0001 | c0001 | t0010 | g0085 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18994 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19006 | hp1 | a0001 | c0001 | t0031 | g0069 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19006 | hp2 | a0001 | c0001 | t0022 | g0210 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19009 | hp1 | a0001 | c0001 | t0049 | g0240 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19043 | hp1 | a0001 | c0001 | t0028 | g0037 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0172 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19055 | hp1 | a0001 | c0001 | t0010 | g0056 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19060 | hp1 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19067 | hp1 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19067 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19075 | hp1 | a0001 | c0001 | t0008 | g0318 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19075 | hp2 | a0001 | c0001 | t0025 | g0101 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19079 | hp2 | a0001 | c0001 | t0023 | g0216 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19084 | hp1 | a0001 | c0001 | t0025 | g0087 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19086 | hp1 | a0001 | c0001 | t0038 | g0211 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19086 | hp2 | a0001 | c0001 | t0030 | g0057 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19088 | hp1 | a0001 | c0001 | t0017 | g0198 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19088 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19089 | hp1 | a0001 | c0001 | t0039 | g0199 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19090 | hp1 | a0001 | c0001 | t0017 | g0222 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | YRI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20129 | hp1 | a0001 | c0001 | t0055 | g0127 | AFR | ASW | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0319 | AFR | ASW | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20752 | hp1 | a0001 | c0001 | t0042 | g0283 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20805 | hp2 | a0001 | c0001 | t0008 | g0313 | EUR | TSI | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0026 | SAS | GIH | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | GIH | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | CLM | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0114 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02486 | hp2 | a0001 | c0001 | t0016 | g0106 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02559 | hp1 | a0001 | c0002 | t0018 | g0156 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG02559 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG06807 | hp1 | a0001 | c0001 | t0014 | g0032 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
HG06807 | hp2 | a0001 | c0001 | t0051 | g0041 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20300 | hp1 | a0001 | c0001 | t0057 | g0118 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | USA | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA21309 | hp1 | a0001 | c0001 | t0014 | g0034 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | LWK | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0179 | REF | REF | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | STAM2_chr2_152111801_152180763 | STAM2 | chr2 | 152111801 | 152180763 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:152116803
|
C | T | 1 | a0001 | 1 | HG01517.hp1 | splice_region_variant | LOW | c.*3771G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | chr2 | 152116803 | ||||||
chr2:152148043
|
C | T | 1 | a0002 | 2 | HG02015.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.281G>A | p.Arg94His | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/14 | 402/5472 | 281/1578 | 94/525 | chr2 | 152148043 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:152123849
|
G | A | 2 | a0001c0002a0001c0004 | 4 | HG02559.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1266C>T | p.Pro422Pro | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/14 | 1387/5472 | 1266/1578 | 422/525 | chr2 | 152123849 | ||
chr2:152123876
|
A | G | 1 | a0001c0004 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1239T>C | p.Thr413Thr | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/14 | 1360/5472 | 1239/1578 | 413/525 | chr2 | 152123876 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:152117109
|
T | C | 4 | a0001c0001t0008a0001c0001t0040a0001c0001t0061others(1): Show | 16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3465A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 3465 | chr2 | 152117109 | |||||
chr2:152117596
|
G | C | 1 | a0001c0001t0014 | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2978C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2978 | chr2 | 152117596 | |||||
chr2:152117656
|
C | T | 1 | a0001c0001t0013 | 6 | HG01074.hp1 HG01192.hp1 HG01256.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2918G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2918 | chr2 | 152117656 | |||||
chr2:152117740
|
A | T | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0017others(14): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2834T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2834 | chr2 | 152117740 | |||||
chr2:152117952
|
T | G | 1 | a0001c0001t0027 | 2 | HG01070.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2622A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2622 | chr2 | 152117952 | |||||
chr2:152118008
|
C | T | 1 | a0001c0001t0042 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2566 | chr2 | 152118008 | |||||
chr2:152118072
|
T | C | 1 | a0001c0001t0049 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2502A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2502 | chr2 | 152118072 | |||||
chr2:152118242
|
C | A | 1 | a0001c0001t0048 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2332 | chr2 | 152118242 | |||||
chr2:152118408
|
T | C | 2 | a0001c0001t0053a0001c0001t0054 | 2 | HG02647.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2166A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2166 | chr2 | 152118408 | |||||
chr2:152118422
|
G | A | 1 | a0001c0001t0043 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2152 | chr2 | 152118422 | |||||
chr2:152118432
|
T | A | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2142 | chr2 | 152118432 | |||||
chr2:152118438
|
C | CTA | 9 | a0001c0001t0010a0001c0001t0017a0001c0001t0022others(6): Show | 23 | HG00408.hp2 HG01256.hp2 HG01517.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2134_*2135dupTA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | |||||
chr2:152118438
|
C | CTATA | 8 | a0001c0001t0004a0001c0001t0014a0001c0001t0023others(5): Show | 41 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2135dupTATA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | |||||
chr2:152118438
|
C | CTATATA | 4 | a0001c0001t0003a0001c0001t0021a0001c0001t0049others(1): Show | 39 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2130_*2135dupTATA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | |||||
chr2:152118438
|
C | CTATATAT others(1): Show |
1 | a0001c0001t0024 | 3 | NA18950.hp2 NA18952.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2135_*2136insTATA others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2135 | chr2 | 152118438 | |||||
chr2:152118443
|
T | C | 1 | a0001c0001t0033 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2131A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2131 | chr2 | 152118443 | |||||
chr2:152118446
|
T | A | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 232 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2128A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2128 | chr2 | 152118446 | |||||
chr2:152118460
|
A | ATATATAT others(1): Show |
1 | a0001c0001t0020 | 4 | HG00639.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | |||||
chr2:152118460
|
A | ATATATG | 1 | a0001c0001t0019 | 4 | HG01891.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | |||||
chr2:152118460
|
A | ATATG | 6 | a0001c0001t0027a0001c0001t0044a0001c0001t0045others(3): Show | 9 | HG01070.hp2 HG01496.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2113_*2114insCATA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | |||||
chr2:152118460
|
A | ATG | 3 | a0001c0001t0012a0001c0001t0053a0001c0001t0056 | 9 | HG00639.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113dupCA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2113 | chr2 | 152118460 | |||||
chr2:152118460
|
A | G | 1 | a0001c0001t0031 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2114T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 2114 | chr2 | 152118460 | |||||
chr2:152118639
|
A | G | 1 | a0001c0001t0044 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1935 | chr2 | 152118639 | |||||
chr2:152118699
|
AT | A | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0014others(15): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1874delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1874 | chr2 | 152118699 | |||||
chr2:152118725
|
T | A | 1 | a0001c0001t0011 | 7 | HG01192.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1849A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1849 | chr2 | 152118725 | |||||
chr2:152118926
|
A | G | 1 | a0001c0001t0035 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1648T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1648 | chr2 | 152118926 | |||||
chr2:152119037
|
G | A | 3 | a0001c0001t0017a0001c0001t0022a0001c0001t0038 | 10 | HG00408.hp2 HG01256.hp2 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1537C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1537 | chr2 | 152119037 | |||||
chr2:152119121
|
T | G | 1 | a0001c0001t0050 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1453 | chr2 | 152119121 | |||||
chr2:152119296
|
T | C | 1 | a0001c0001t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1278 | chr2 | 152119296 | |||||
chr2:152119332
|
A | G | 1 | a0001c0001t0041 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1242 | chr2 | 152119332 | |||||
chr2:152119488
|
G | C | 21 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(18): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1086C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 1086 | chr2 | 152119488 | |||||
chr2:152119597
|
C | A | 1 | a0001c0001t0026 | 2 | HG03239.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*977G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 977 | chr2 | 152119597 | |||||
chr2:152119721
|
A | T | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 853 | chr2 | 152119721 | |||||
chr2:152119722
|
T | A | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 852 | chr2 | 152119722 | |||||
chr2:152119723
|
A | G | 1 | a0001c0001t0030 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 851 | chr2 | 152119723 | |||||
chr2:152120079
|
A | T | 1 | a0001c0001t0055 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 495 | chr2 | 152120079 | |||||
chr2:152120161
|
T | G | 3 | a0001c0001t0017a0001c0001t0022a0001c0001t0038 | 10 | HG00408.hp2 HG01256.hp2 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*413A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 413 | chr2 | 152120161 | |||||
chr2:152120189
|
T | A | 53 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(50): Show | 250 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*385A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 385 | chr2 | 152120189 | |||||
chr2:152120222
|
A | G | 4 | a0001c0001t0008a0001c0001t0040a0001c0001t0061others(1): Show | 16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*352T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 352 | chr2 | 152120222 | |||||
chr2:152120254
|
T | A | 2 | a0001c0001t0053a0001c0001t0054 | 2 | HG02647.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 320 | chr2 | 152120254 | |||||
chr2:152120317
|
C | G | 1 | a0001c0001t0032 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 257 | chr2 | 152120317 | |||||
chr2:152120392
|
A | T | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 182 | chr2 | 152120392 | |||||
chr2:152120395
|
G | GA | 8 | a0001c0001t0015a0001c0001t0021a0001c0001t0022others(5): Show | 19 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*178dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 178 | chr2 | 152120395 | |||||
chr2:152120395
|
GA | G | 17 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(14): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*178delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 178 | chr2 | 152120395 | |||||
chr2:152120395
|
GAA | G | 4 | a0001c0001t0005a0001c0001t0010a0001c0001t0030others(1): Show | 30 | HG00408.hp1 HG00673.hp1 HG01978.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*177_*178delTT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 177 | chr2 | 152120395 | |||||
chr2:152120407
|
A | C | 1 | a0001c0001t0029 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 167 | chr2 | 152120407 | |||||
chr2:152120464
|
C | A | 1 | a0001c0001t0059 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 110 | chr2 | 152120464 | |||||
chr2:152120544
|
A | G | 2 | a0001c0001t0016a0001c0001t0028 | 6 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 30 | chr2 | 152120544 | |||||
chr2:152120562
|
C | T | 1 | a0001c0001t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 14/14 | 12 | chr2 | 152120562 | |||||
chr2:152175694
|
T | C | 4 | a0001c0001t0008a0001c0001t0060a0001c0001t0061others(1): Show | 16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/14 | 52 | chr2 | 152175694 | |||||
chr2:152175763
|
T | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/14 | 121 | chr2 | 152175763 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:152120907
|
T | TA | 7 | a0001c0001t0019g0157a0001c0001t0019g0158a0001c0001t0045g0159others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-106dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120907 | ||||||
chr2:152120948
|
C | A | 2 | a0001c0001t0053g0097a0001c0001t0054g0098 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1350-146G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120948 | ||||||
chr2:152120963
|
A | C | 1 | a0001c0001t0009g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1350-161T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152120963 | ||||||
chr2:152121238
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1350-436G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121238 | ||||||
chr2:152121256
|
G | A | 1 | a0001c0001t0017g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1350-454C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121256 | ||||||
chr2:152121447
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1350-645T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121447 | ||||||
chr2:152121474
|
G | A | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1350-672C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121474 | ||||||
chr2:152121646
|
CTA | C | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350-846_1350-845d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121646 | ||||||
chr2:152121752
|
T | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0078a0001c0001t0002g0096others(2): Show | 7 | NA18747.hp2 NA18941.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350-950A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121752 | ||||||
chr2:152121770
|
A | C | 189 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(186): Show | 210 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1350-968T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121770 | ||||||
chr2:152121820
|
G | A | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1350-1018C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121820 | ||||||
chr2:152121827
|
G | A | 112 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0003g0017others(109): Show | 119 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1350-1025C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121827 | ||||||
chr2:152121919
|
G | A | 12 | a0001c0001t0007g0009a0001c0001t0007g0040a0001c0001t0007g0117others(9): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1350-1117C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121919 | ||||||
chr2:152121921
|
G | A | 2 | a0001c0001t0006g0129a0001c0001t0063g0130 | 2 | NA18970.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1350-1119C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121921 | ||||||
chr2:152121974
|
G | C | 1 | a0001c0001t0011g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1350-1172C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152121974 | ||||||
chr2:152122049
|
A | C | 18 | a0001c0001t0002g0074a0001c0001t0008g0027a0001c0001t0008g0308others(15): Show | 19 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1350-1247T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122049 | ||||||
chr2:152122057
|
A | T | 23 | a0001c0001t0006g0151a0001c0001t0007g0116a0001c0001t0012g0161others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1350-1255T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | ||||||
chr2:152122057
|
AAT | A | 24 | a0001c0001t0001g0259a0001c0001t0002g0080a0001c0001t0002g0089others(21): Show | 25 | HG02145.hp1 HG02155.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1350-1257_1350-125 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | ||||||
chr2:152122057
|
AATAT | A | 73 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(70): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1350-1259_1350-125 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122057 | ||||||
chr2:152122058
|
AT | A | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0034others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-1257delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122058 | ||||||
chr2:152122058
|
ATAT | A | 3 | a0001c0001t0003g0248a0001c0001t0014g0033a0001c0001t0014g0036 | 3 | HG01167.hp2 HG02896.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1350-1259_1350-125 others(7): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122058 | ||||||
chr2:152122059
|
T | A | 80 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(77): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1350-1257A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122059 | ||||||
chr2:152122061
|
T | A | 86 | a0001c0001t0003g0017a0001c0001t0003g0183a0001c0001t0003g0184others(83): Show | 92 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1350-1259A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122061 | ||||||
chr2:152122063
|
T | A | 2 | a0001c0001t0002g0074a0001c0001t0003g0248 | 2 | HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1350-1261A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122063 | ||||||
chr2:152122065
|
T | A | 1 | a0001c0001t0003g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1350-1263A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122065 | ||||||
chr2:152122072
|
A | ATG | 9 | a0001c0001t0006g0303a0001c0001t0007g0009a0001c0001t0007g0117others(6): Show | 11 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1350-1271_1350-127 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | ||||||
chr2:152122072
|
A | ATGTG | 4 | a0001c0001t0006g0141a0001c0001t0007g0300a0001c0001t0011g0144others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1271_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | ||||||
chr2:152122072
|
A | G | 4 | a0001c0001t0012g0161a0001c0001t0027g0160a0001c0001t0027g0164others(1): Show | 4 | HG01070.hp2 HG01496.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1270T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122072 | ||||||
chr2:152122074
|
A | ATGTG | 16 | a0001c0001t0001g0139a0001c0001t0006g0026a0001c0001t0006g0129others(13): Show | 17 | HG01081.hp2 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1350-1273_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | ||||||
chr2:152122074
|
A | G | 36 | a0001c0001t0006g0141a0001c0001t0006g0303a0001c0001t0007g0009others(33): Show | 38 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1350-1272T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | ||||||
chr2:152122074
|
ATATGTG | A | 79 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(76): Show | 85 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1350-1278_1350-127 others(10): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122074 | ||||||
chr2:152122076
|
A | ATG | 3 | a0001c0001t0007g0121a0001c0001t0013g0293a0001c0001t0041g0284 | 3 | HG02080.hp1 HG02683.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1350-1276_1350-127 others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | ||||||
chr2:152122076
|
A | G | 85 | a0001c0001t0001g0022a0001c0001t0001g0134a0001c0001t0001g0139others(82): Show | 91 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1350-1274T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | ||||||
chr2:152122076
|
ATGTG | A | 7 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-1278_1350-127 others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122076 | ||||||
chr2:152122078
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0262a0001c0001t0003g0248 | 4 | HG03688.hp2 NA18960.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350-1276C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122078 | ||||||
chr2:152122145
|
G | T | 1 | a0001c0001t0003g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1350-1343C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122145 | ||||||
chr2:152122166
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1350-1364G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122166 | ||||||
chr2:152122289
|
G | A | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(95): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+1477C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122289 | ||||||
chr2:152122330
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1349+1436A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122330 | ||||||
chr2:152122349
|
C | T | 1 | a0001c0001t0020g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1349+1417G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122349 | ||||||
chr2:152122433
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1349+1333T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122433 | ||||||
chr2:152122488
|
G | A | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1349+1278C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122488 | ||||||
chr2:152122525
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1349+1241G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122525 | ||||||
chr2:152122558
|
T | C | 1 | a0001c0001t0019g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1349+1208A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122558 | ||||||
chr2:152122605
|
T | A | 2 | a0001c0001t0003g0184a0001c0001t0003g0237 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1349+1161A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152122605 | ||||||
chr2:152123062
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1349+704G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123062 | ||||||
chr2:152123094
|
C | T | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1349+672G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123094 | ||||||
chr2:152123134
|
T | C | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1349+632A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123134 | ||||||
chr2:152123181
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1349+585G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123181 | ||||||
chr2:152123199
|
G | A | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(95): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+567C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123199 | ||||||
chr2:152123232
|
C | T | 2 | a0001c0001t0053g0097a0001c0001t0054g0098 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1349+534G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123232 | ||||||
chr2:152123243
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1349+523C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123243 | ||||||
chr2:152123305
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1349+461C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123305 | ||||||
chr2:152123335
|
G | GT | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1349+430_1349+431i others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123335 | ||||||
chr2:152123355
|
G | C | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(95): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1349+411C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123355 | ||||||
chr2:152123358
|
G | A | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1349+408C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123358 | ||||||
chr2:152123411
|
A | C | 1 | a0001c0001t0008g0313 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1349+355T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123411 | ||||||
chr2:152123419
|
C | T | 113 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(110): Show | 119 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1349+347G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123419 | ||||||
chr2:152123464
|
G | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1349+302C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123464 | ||||||
chr2:152123504
|
C | A | 1 | a0001c0001t0004g0238 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1349+262G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123504 | ||||||
chr2:152123646
|
C | T | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1349+120G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123646 | ||||||
chr2:152123732
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1349+34G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123732 | ||||||
chr2:152123751
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0054g0098 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1349+15C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 13/13 | chr2 | 152123751 | ||||||
chr2:152124063
|
T | C | 1 | a0001c0001t0013g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1180-128A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124063 | ||||||
chr2:152124339
|
T | A | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1180-404A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124339 | ||||||
chr2:152124761
|
A | C | 2 | a0001c0001t0027g0160a0001c0001t0027g0164 | 2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1180-826T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124761 | ||||||
chr2:152124766
|
C | T | 145 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(142): Show | 163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1180-831G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124766 | ||||||
chr2:152124821
|
G | T | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(95): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1180-886C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124821 | ||||||
chr2:152124828
|
C | T | 1 | a0001c0001t0058g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1180-893G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124828 | ||||||
chr2:152124869
|
T | C | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1180-934A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124869 | ||||||
chr2:152124889
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1180-954G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124889 | ||||||
chr2:152124954
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1180-1019A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152124954 | ||||||
chr2:152125041
|
A | G | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-1106T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125041 | ||||||
chr2:152125109
|
A | C | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1179+1117T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125109 | ||||||
chr2:152125313
|
G | A | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1179+913C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125313 | ||||||
chr2:152125492
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1179+734A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125492 | ||||||
chr2:152125547
|
G | GT | 3 | a0001c0001t0001g0115a0001c0001t0015g0113a0001c0001t0015g0114 | 3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+678dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125547 | ||||||
chr2:152125691
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1179+535A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125691 | ||||||
chr2:152125910
|
G | T | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1179+316C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152125910 | ||||||
chr2:152126057
|
G | C | 1 | a0001c0001t0005g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1179+169C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 12/13 | chr2 | 152126057 | ||||||
chr2:152126516
|
C | T | 1 | a0001c0001t0014g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1026-137G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126516 | ||||||
chr2:152126536
|
G | T | 1 | a0001c0001t0005g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1026-157C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126536 | ||||||
chr2:152126570
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026-191A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126570 | ||||||
chr2:152126692
|
A | T | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026-313T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126692 | ||||||
chr2:152126712
|
A | AC | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1026-334dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126712 | ||||||
chr2:152126765
|
A | T | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1026-386T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126765 | ||||||
chr2:152126852
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1026-473C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152126852 | ||||||
chr2:152127196
|
A | G | 7 | a0001c0001t0019g0157a0001c0001t0019g0158a0001c0001t0045g0159others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-817T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127196 | ||||||
chr2:152127234
|
TG | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1026-856delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127234 | ||||||
chr2:152127401
|
A | C | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026-1022T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127401 | ||||||
chr2:152127687
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026-1308A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127687 | ||||||
chr2:152127719
|
C | T | 2 | a0001c0001t0023g0196a0001c0001t0039g0199 | 2 | NA18963.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1026-1340G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127719 | ||||||
chr2:152127797
|
A | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026-1418T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127797 | ||||||
chr2:152127849
|
T | C | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1026-1470A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152127849 | ||||||
chr2:152128000
|
C | T | 9 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(6): Show | 9 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1621G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128000 | ||||||
chr2:152128022
|
C | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1026-1643G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128022 | ||||||
chr2:152128051
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1026-1672G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128051 | ||||||
chr2:152128130
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1026-1751C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128130 | ||||||
chr2:152128399
|
C | T | 1 | a0001c0001t0006g0131 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1026-2020G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128399 | ||||||
chr2:152128417
|
T | TA | 4 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0269others(1): Show | 7 | HG02056.hp1 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-2039dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128417 | ||||||
chr2:152128418
|
A | T | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1026-2039T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128418 | ||||||
chr2:152128460
|
GA | G | 15 | a0001c0001t0008g0027a0001c0001t0008g0308a0001c0001t0008g0309others(12): Show | 16 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026-2082delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128460 | ||||||
chr2:152128599
|
T | C | 1 | a0001c0001t0025g0087 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1026-2220A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128599 | ||||||
chr2:152128643
|
C | T | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1026-2264G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128643 | ||||||
chr2:152128885
|
T | TAGGAATA others(5): Show |
1 | a0001c0001t0001g0291 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1026-2518_1026-250 others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128885 | ||||||
chr2:152128965
|
G | C | 1 | a0001c0001t0041g0284 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1026-2586C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152128965 | ||||||
chr2:152129055
|
T | G | 1 | a0001c0001t0007g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1026-2676A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129055 | ||||||
chr2:152129527
|
T | C | 93 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(90): Show | 99 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1025+2587A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129527 | ||||||
chr2:152129667
|
C | T | 2 | a0001c0001t0003g0183a0001c0001t0003g0244 | 2 | HG04184.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1025+2447G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129667 | ||||||
chr2:152129686
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1025+2428G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129686 | ||||||
chr2:152129740
|
A | C | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1025+2374T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129740 | ||||||
chr2:152129749
|
A | C | 1 | a0001c0001t0043g0289 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1025+2365T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129749 | ||||||
chr2:152129784
|
C | T | 4 | a0001c0001t0009g0046a0001c0001t0009g0047a0001c0001t0009g0048others(1): Show | 4 | HG02145.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+2330G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129784 | ||||||
chr2:152129832
|
T | C | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1025+2282A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129832 | ||||||
chr2:152129838
|
A | G | 1 | a0001c0001t0008g0312 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1025+2276T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129838 | ||||||
chr2:152129862
|
T | C | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2252A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129862 | ||||||
chr2:152129985
|
A | G | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1025+2129T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152129985 | ||||||
chr2:152130079
|
C | T | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1025+2035G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130079 | ||||||
chr2:152130095
|
A | G | 2 | a0001c0001t0016g0028a0001c0001t0016g0029 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1025+2019T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130095 | ||||||
chr2:152130288
|
T | G | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025+1826A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130288 | ||||||
chr2:152130290
|
T | C | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1025+1824A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130290 | ||||||
chr2:152130337
|
C | T | 1 | a0001c0001t0004g0242 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1025+1777G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130337 | ||||||
chr2:152130465
|
A | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1025+1649T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130465 | ||||||
chr2:152130541
|
G | A | 4 | a0001c0001t0008g0309a0001c0001t0008g0310a0001c0001t0008g0313others(1): Show | 4 | HG01081.hp1 HG01109.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+1573C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130541 | ||||||
chr2:152130542
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(61): Show | 78 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1025+1572G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130542 | ||||||
chr2:152130694
|
A | T | 3 | a0001c0001t0019g0172a0001c0001t0020g0173a0001c0001t0020g0174 | 3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1025+1420T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130694 | ||||||
chr2:152130995
|
CA | C | 302 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(299): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1025+1118delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152130995 | ||||||
chr2:152131032
|
A | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1025+1082T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131032 | ||||||
chr2:152131589
|
T | C | 12 | a0001c0001t0007g0009a0001c0001t0007g0040a0001c0001t0007g0117others(9): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1025+525A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131589 | ||||||
chr2:152131619
|
G | C | 2 | a0001c0001t0053g0097a0001c0001t0054g0098 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1025+495C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131619 | ||||||
chr2:152131635
|
G | A | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1025+479C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131635 | ||||||
chr2:152131755
|
G | C | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1025+359C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131755 | ||||||
chr2:152131872
|
T | C | 1 | a0001c0001t0040g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1025+242A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152131872 | ||||||
chr2:152132044
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1025+70A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132044 | ||||||
chr2:152132096
|
C | CT | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1025+17dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132096 | ||||||
chr2:152132101
|
C | T | 1 | a0001c0001t0019g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1025+13G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 11/13 | chr2 | 152132101 | ||||||
chr2:152132242
|
A | G | 3 | a0001c0001t0004g0253a0001c0001t0023g0196a0001c0001t0039g0199 | 3 | NA18963.hp1 NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.971-74T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132242 | ||||||
chr2:152132515
|
T | C | 3 | a0001c0001t0007g0120a0001c0001t0007g0121a0001c0001t0007g0125 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.971-347A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132515 | ||||||
chr2:152132628
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.971-460A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132628 | ||||||
chr2:152132663
|
TAAG | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.971-498_971-496del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132663 | ||||||
chr2:152132785
|
CTA | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.970+386_970+387del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152132785 | ||||||
chr2:152133000
|
G | A | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.970+173C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 10/13 | chr2 | 152133000 | ||||||
chr2:152133537
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0015g0113a0001c0001t0015g0114 | 3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.800-53C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133537 | ||||||
chr2:152133790
|
T | C | 1 | a0001c0001t0019g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.800-306A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133790 | ||||||
chr2:152133844
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.800-360C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133844 | ||||||
chr2:152133932
|
C | G | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.800-448G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152133932 | ||||||
chr2:152134007
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.800-523A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134007 | ||||||
chr2:152134104
|
TG | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.800-621delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134104 | ||||||
chr2:152134207
|
T | C | 3 | a0001c0001t0007g0122a0001c0001t0007g0123a0001c0001t0007g0124 | 3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.800-723A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134207 | ||||||
chr2:152134207
|
T | G | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.800-723A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134207 | ||||||
chr2:152134352
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.800-868G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134352 | ||||||
chr2:152134418
|
A | G | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.800-934T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134418 | ||||||
chr2:152134449
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-965G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134449 | ||||||
chr2:152134841
|
G | A | 2 | a0001c0001t0003g0228a0001c0002t0018g0155 | 2 | HG03540.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.799+668C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134841 | ||||||
chr2:152134930
|
G | A | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+579C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134930 | ||||||
chr2:152134946
|
T | C | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799+563A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134946 | ||||||
chr2:152134988
|
G | T | 1 | a0001c0001t0033g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.799+521C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134988 | ||||||
chr2:152134993
|
C | T | 5 | a0001c0001t0013g0025a0001c0001t0013g0255a0001c0001t0013g0293others(2): Show | 6 | HG01074.hp1 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.799+516G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152134993 | ||||||
chr2:152135401
|
AT | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.799+107delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152135401 | ||||||
chr2:152135449
|
A | G | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+60T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 8/13 | chr2 | 152135449 | ||||||
chr2:152135651
|
C | CAATA | 66 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(63): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.705-52_705-49dupTA others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135651 | ||||||
chr2:152135723
|
G | A | 189 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(186): Show | 210 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.705-120C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135723 | ||||||
chr2:152135781
|
C | T | 1 | a0001c0001t0016g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.705-178G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135781 | ||||||
chr2:152135856
|
A | G | 1 | a0001c0001t0026g0021 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.705-253T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135856 | ||||||
chr2:152135868
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.705-265A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135868 | ||||||
chr2:152135919
|
A | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.705-316T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135919 | ||||||
chr2:152135998
|
G | A | 189 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(186): Show | 210 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.705-395C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152135998 | ||||||
chr2:152136005
|
G | A | 2 | a0001c0001t0004g0197a0001c0001t0004g0205 | 2 | NA18974.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.705-402C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136005 | ||||||
chr2:152136088
|
C | CA | 10 | a0001c0001t0001g0139a0001c0001t0001g0277a0001c0001t0003g0220others(7): Show | 10 | HG00621.hp2 HG00741.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-486dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136088 | ||||||
chr2:152136088
|
CA | C | 6 | a0001c0001t0001g0267a0001c0001t0001g0285a0001c0001t0003g0228others(3): Show | 6 | HG01069.hp1 HG01943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-486delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136088 | ||||||
chr2:152136214
|
G | A | 2 | a0001c0001t0027g0160a0001c0001t0027g0164 | 2 | HG01070.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.705-611C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136214 | ||||||
chr2:152136246
|
T | A | 1 | a0001c0001t0001g0020 | 2 | NA18944.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.705-643A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136246 | ||||||
chr2:152136262
|
G | A | 1 | a0001c0001t0062g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.705-659C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136262 | ||||||
chr2:152136515
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.705-912G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136515 | ||||||
chr2:152136620
|
A | AACAG | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.705-1021_705-1018d others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136620 | ||||||
chr2:152136784
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.705-1181G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136784 | ||||||
chr2:152136892
|
C | CT | 8 | a0001c0001t0001g0277a0001c0001t0001g0287a0001c0001t0002g0060others(5): Show | 8 | HG00741.hp1 HG01261.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.705-1290dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136892 | ||||||
chr2:152136892
|
CT | C | 24 | a0001c0001t0005g0039a0001c0001t0012g0161a0001c0001t0012g0162others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.705-1290delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136892 | ||||||
chr2:152136897
|
T | C | 91 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(88): Show | 97 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.705-1294A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136897 | ||||||
chr2:152136900
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.705-1297A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152136900 | ||||||
chr2:152137337
|
G | C | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-1734C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137337 | ||||||
chr2:152137596
|
T | C | 124 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(121): Show | 139 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.705-1993A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137596 | ||||||
chr2:152137602
|
T | C | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.705-1999A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137602 | ||||||
chr2:152137738
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.705-2135A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137738 | ||||||
chr2:152137818
|
T | G | 1 | a0001c0001t0002g0075 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.705-2215A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152137818 | ||||||
chr2:152138100
|
G | T | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-2497C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138100 | ||||||
chr2:152138216
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.705-2613A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138216 | ||||||
chr2:152138330
|
T | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0291a0001c0001t0015g0290 | 5 | HG02055.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.705-2727A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138330 | ||||||
chr2:152138401
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.705-2798A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138401 | ||||||
chr2:152138456
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.705-2853A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138456 | ||||||
chr2:152138663
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.705-3060G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138663 | ||||||
chr2:152138747
|
T | G | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.705-3144A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138747 | ||||||
chr2:152138755
|
T | C | 3 | a0001c0001t0007g0122a0001c0001t0007g0123a0001c0001t0007g0124 | 3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.705-3152A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138755 | ||||||
chr2:152138948
|
C | A | 1 | a0001c0001t0030g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.705-3345G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152138948 | ||||||
chr2:152139031
|
C | T | 1 | a0001c0001t0006g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.705-3428G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139031 | ||||||
chr2:152139197
|
T | G | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.705-3594A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139197 | ||||||
chr2:152139380
|
G | C | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.705-3777C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139380 | ||||||
chr2:152139445
|
T | C | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.705-3842A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139445 | ||||||
chr2:152139841
|
A | G | 2 | a0001c0001t0017g0198a0001c0001t0017g0204 | 2 | NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.704+3986T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139841 | ||||||
chr2:152139858
|
TAATACAA others(15): Show |
T | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.704+3947_704+3968d others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139858 | ||||||
chr2:152139902
|
T | C | 3 | a0001c0001t0002g0102a0001c0001t0036g0088a0001c0001t0060g0307 | 3 | HG02027.hp2 HG02165.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.704+3925A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139902 | ||||||
chr2:152139911
|
C | G | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704+3916G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139911 | ||||||
chr2:152139991
|
C | T | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.704+3836G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152139991 | ||||||
chr2:152140005
|
G | A | 1 | a0001c0001t0021g0232 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.704+3822C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140005 | ||||||
chr2:152140460
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.704+3367G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140460 | ||||||
chr2:152140905
|
C | T | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.704+2922G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140905 | ||||||
chr2:152140990
|
T | A | 1 | a0001c0001t0008g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+2837A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152140990 | ||||||
chr2:152141040
|
G | A | 1 | a0001c0001t0008g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+2787C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141040 | ||||||
chr2:152141138
|
C | CAA | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.704+2687_704+2688d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | ||||||
chr2:152141138
|
CA | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.704+2688delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | ||||||
chr2:152141138
|
CAA | C | 13 | a0001c0001t0001g0139a0001c0001t0001g0280a0001c0001t0002g0060others(10): Show | 13 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.704+2687_704+2688d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141138 | ||||||
chr2:152141212
|
G | A | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.704+2615C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141212 | ||||||
chr2:152141288
|
C | A | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+2539G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141288 | ||||||
chr2:152141459
|
A | G | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+2368T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141459 | ||||||
chr2:152141521
|
A | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.704+2306T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141521 | ||||||
chr2:152141545
|
T | C | 1 | a0001c0001t0017g0198 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.704+2282A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141545 | ||||||
chr2:152141558
|
C | A | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704+2269G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141558 | ||||||
chr2:152141574
|
A | C | 1 | a0001c0001t0016g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.704+2253T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141574 | ||||||
chr2:152141581
|
T | G | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+2246A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141581 | ||||||
chr2:152141592
|
T | C | 14 | a0001c0001t0008g0027a0001c0001t0008g0308a0001c0001t0008g0309others(11): Show | 15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.704+2235A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141592 | ||||||
chr2:152141629
|
C | T | 2 | a0001c0001t0007g0009a0001c0001t0007g0300 | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+2198G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141629 | ||||||
chr2:152141639
|
G | C | 2 | a0001c0001t0007g0009a0001c0001t0007g0300 | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+2188C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141639 | ||||||
chr2:152141674
|
T | G | 1 | a0001c0001t0003g0301 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.704+2153A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141674 | ||||||
chr2:152141717
|
A | G | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+2110T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141717 | ||||||
chr2:152141739
|
C | T | 1 | a0001c0001t0009g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704+2088G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141739 | ||||||
chr2:152141751
|
C | T | 1 | a0001c0001t0040g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.704+2076G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141751 | ||||||
chr2:152141811
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.704+2016C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141811 | ||||||
chr2:152141929
|
TTTCAAGG others(3): Show |
T | 2 | a0001c0001t0002g0003a0001c0001t0025g0087 | 4 | NA18941.hp2 NA18983.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.704+1888_704+1897d others(12): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141929 | ||||||
chr2:152141953
|
T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.704+1874A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141953 | ||||||
chr2:152141972
|
C | T | 1 | a0001c0001t0015g0114 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704+1855G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152141972 | ||||||
chr2:152142038
|
G | A | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.704+1789C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142038 | ||||||
chr2:152142082
|
C | T | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+1745G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142082 | ||||||
chr2:152142087
|
G | A | 7 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1740C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142087 | ||||||
chr2:152142209
|
T | G | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+1618A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142209 | ||||||
chr2:152142316
|
A | G | 1 | a0001c0001t0058g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704+1511T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142316 | ||||||
chr2:152142480
|
G | C | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704+1347C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142480 | ||||||
chr2:152142547
|
T | A | 3 | a0001c0001t0019g0172a0001c0001t0020g0173a0001c0001t0020g0174 | 3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.704+1280A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142547 | ||||||
chr2:152142622
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1205T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142622 | ||||||
chr2:152142623
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1204A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142623 | ||||||
chr2:152142625
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704+1202T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142625 | ||||||
chr2:152142833
|
T | C | 1 | a0001c0001t0020g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704+994A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142833 | ||||||
chr2:152142853
|
T | C | 1 | a0001c0001t0016g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.704+974A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152142853 | ||||||
chr2:152143111
|
A | G | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.704+716T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143111 | ||||||
chr2:152143179
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.704+648G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143179 | ||||||
chr2:152143339
|
A | G | 2 | a0001c0001t0003g0190a0001c0001t0003g0249 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.704+488T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143339 | ||||||
chr2:152143481
|
G | A | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.704+346C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143481 | ||||||
chr2:152143576
|
T | C | 4 | a0001c0001t0001g0260a0001c0001t0001g0296a0001c0001t0015g0278others(1): Show | 5 | HG01168.hp2 HG02735.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.704+251A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143576 | ||||||
chr2:152143619
|
A | T | 2 | a0001c0001t0007g0117a0001c0001t0057g0118 | 2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.704+208T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143619 | ||||||
chr2:152143823
|
T | A | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
splice_region_variant&intron_variant | LOW | c.704+4A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 7/13 | chr2 | 152143823 | ||||||
chr2:152144081
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.518-68A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144081 | ||||||
chr2:152144199
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.518-186A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144199 | ||||||
chr2:152144421
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.518-408A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144421 | ||||||
chr2:152144462
|
T | C | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+426A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144462 | ||||||
chr2:152144532
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.517+356G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144532 | ||||||
chr2:152144564
|
G | C | 81 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(78): Show | 96 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.517+324C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144564 | ||||||
chr2:152144595
|
G | C | 1 | a0001c0001t0003g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517+293C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144595 | ||||||
chr2:152144607
|
T | C | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.517+281A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144607 | ||||||
chr2:152144683
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0103 | 2 | NA18747.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.517+205G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144683 | ||||||
chr2:152144684
|
G | A | 3 | a0001c0001t0007g0120a0001c0001t0007g0121a0001c0001t0007g0125 | 3 | HG02717.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.517+204C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144684 | ||||||
chr2:152144828
|
C | T | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517+60G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144828 | ||||||
chr2:152144845
|
GAT | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.517+41_517+42delAT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 6/13 | chr2 | 152144845 | ||||||
chr2:152145096
|
G | C | 1 | a0001c0001t0008g0316 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.448-139C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145096 | ||||||
chr2:152145128
|
T | C | 1 | a0001c0001t0020g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.448-171A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145128 | ||||||
chr2:152145232
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448-275C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145232 | ||||||
chr2:152145280
|
G | T | 169 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(166): Show | 187 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.448-323C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145280 | ||||||
chr2:152145405
|
G | GT | 14 | a0001c0001t0008g0027a0001c0001t0008g0308a0001c0001t0008g0309others(11): Show | 15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-449dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145405 | ||||||
chr2:152145544
|
A | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.448-587T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145544 | ||||||
chr2:152145986
|
T | C | 1 | a0001c0001t0043g0289 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.448-1029A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152145986 | ||||||
chr2:152146113
|
T | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.447+1049A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146113 | ||||||
chr2:152146271
|
C | CA | 70 | a0001c0001t0001g0115a0001c0001t0001g0134a0001c0001t0002g0054others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.447+890dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | ||||||
chr2:152146271
|
C | CAA | 82 | a0001c0001t0001g0139a0001c0001t0003g0017a0001c0001t0003g0179others(79): Show | 88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.447+889_447+890dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | ||||||
chr2:152146271
|
C | CAAAA | 7 | a0001c0001t0003g0248a0001c0001t0014g0031a0001c0001t0014g0032others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+887_447+890dup others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | ||||||
chr2:152146271
|
CA | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0256a0001c0001t0001g0258others(14): Show | 19 | HG01069.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+890delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146271 | ||||||
chr2:152146291
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+871A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146291 | ||||||
chr2:152146292
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+870G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146292 | ||||||
chr2:152146293
|
T | C | 1 | a0001c0001t0002g0053 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.447+869A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146293 | ||||||
chr2:152146348
|
G | A | 1 | a0001c0001t0011g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.447+814C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146348 | ||||||
chr2:152146413
|
A | G | 1 | a0001c0001t0003g0228 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.447+749T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146413 | ||||||
chr2:152146590
|
G | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.447+572C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146590 | ||||||
chr2:152146760
|
G | A | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.447+402C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146760 | ||||||
chr2:152146877
|
G | T | 1 | a0001c0001t0003g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.447+285C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146877 | ||||||
chr2:152146885
|
G | A | 1 | a0001c0001t0010g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.447+277C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146885 | ||||||
chr2:152146898
|
T | C | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.447+264A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146898 | ||||||
chr2:152146932
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.447+230C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146932 | ||||||
chr2:152146957
|
T | C | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.447+205A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152146957 | ||||||
chr2:152147069
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.447+93A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 5/13 | chr2 | 152147069 | ||||||
chr2:152147421
|
A | C | 1 | a0001c0001t0004g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.301-113T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147421 | ||||||
chr2:152147634
|
T | C | 5 | a0001c0001t0003g0183a0001c0001t0003g0244a0001c0001t0004g0242others(2): Show | 5 | HG00609.hp1 HG04184.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-326A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147634 | ||||||
chr2:152147700
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 12 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.300+324A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147700 | ||||||
chr2:152147739
|
G | A | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.300+285C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147739 | ||||||
chr2:152147758
|
A | G | 2 | a0001c0001t0047g0178a0001c0001t0050g0182 | 2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.300+266T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147758 | ||||||
chr2:152147768
|
A | G | 3 | a0001c0001t0007g0122a0001c0001t0007g0123a0001c0001t0007g0124 | 3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.300+256T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147768 | ||||||
chr2:152147804
|
C | G | 1 | a0001c0001t0005g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.300+220G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147804 | ||||||
chr2:152147832
|
A | G | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.300+192T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147832 | ||||||
chr2:152147871
|
C | A | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.300+153G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147871 | ||||||
chr2:152147982
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.300+42T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 4/13 | chr2 | 152147982 | ||||||
chr2:152148167
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0291a0001c0001t0015g0290 | 5 | HG02055.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-45T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 3/13 | chr2 | 152148167 | ||||||
chr2:152148222
|
C | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.201+3G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 3/13 | chr2 | 152148222 | ||||||
chr2:152148453
|
T | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.126-153A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152148453 | ||||||
chr2:152148970
|
G | A | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.126-670C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152148970 | ||||||
chr2:152149330
|
A | G | 187 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(184): Show | 208 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.125+815T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149330 | ||||||
chr2:152149432
|
C | G | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.125+713G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149432 | ||||||
chr2:152149490
|
T | C | 1 | a0001c0001t0007g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+655A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149490 | ||||||
chr2:152149496
|
CT | C | 178 | a0001c0001t0001g0257a0001c0001t0001g0267a0001c0001t0002g0001others(175): Show | 199 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.125+648delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149496 | ||||||
chr2:152149496
|
CTT | C | 10 | a0001c0001t0004g0188a0001c0001t0014g0031a0001c0001t0014g0032others(7): Show | 10 | HG01167.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+647_125+648del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149496 | ||||||
chr2:152149525
|
T | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.125+620A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149525 | ||||||
chr2:152149549
|
G | A | 1 | a0001c0001t0008g0320 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.125+596C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149549 | ||||||
chr2:152149573
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG01123.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.125+572G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149573 | ||||||
chr2:152149745
|
G | A | 1 | a0001c0001t0005g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+400C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149745 | ||||||
chr2:152149867
|
T | C | 9 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(6): Show | 9 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+278A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149867 | ||||||
chr2:152149938
|
G | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.125+207C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152149938 | ||||||
chr2:152150019
|
T | G | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125+126A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150019 | ||||||
chr2:152150049
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125+96A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150049 | ||||||
chr2:152150090
|
G | A | 1 | a0001c0001t0002g0128 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.125+55C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 2/13 | chr2 | 152150090 | ||||||
chr2:152150286
|
T | C | 1 | a0001c0001t0052g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.41-57A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150286 | ||||||
chr2:152150519
|
C | T | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.41-290G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150519 | ||||||
chr2:152150520
|
A | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-291T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152150520 | ||||||
chr2:152151048
|
G | A | 2 | a0001c0001t0010g0084a0001c0001t0010g0085 | 2 | NA18982.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.41-819C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151048 | ||||||
chr2:152151093
|
G | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-864C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151093 | ||||||
chr2:152151178
|
C | CT | 12 | a0001c0001t0001g0270a0001c0001t0007g0120a0001c0001t0007g0121others(9): Show | 12 | HG01167.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.41-950dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151178 | ||||||
chr2:152151178
|
CT | C | 8 | a0001c0001t0001g0256a0001c0001t0007g0009a0001c0001t0007g0117others(5): Show | 10 | HG01891.hp1 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-950delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151178 | ||||||
chr2:152151196
|
T | C | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(95): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.41-967A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151196 | ||||||
chr2:152151196
|
T | TC | 4 | a0001c0001t0005g0070a0001c0001t0016g0106a0001c0001t0016g0107others(1): Show | 4 | HG02486.hp2 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-968dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151196 | ||||||
chr2:152151349
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-1120A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151349 | ||||||
chr2:152151422
|
C | T | 3 | a0001c0001t0004g0253a0001c0001t0010g0084a0001c0001t0010g0085 | 3 | NA18982.hp1 NA18994.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.41-1193G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151422 | ||||||
chr2:152151511
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0023 | 5 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-1282C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151511 | ||||||
chr2:152151573
|
T | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-1344A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151573 | ||||||
chr2:152151609
|
T | C | 2 | a0001c0001t0016g0028a0001c0001t0016g0029 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41-1380A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151609 | ||||||
chr2:152151692
|
C | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-1463G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151692 | ||||||
chr2:152151737
|
G | A | 1 | a0001c0001t0004g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.41-1508C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152151737 | ||||||
chr2:152152192
|
C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-1963G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152192 | ||||||
chr2:152152279
|
G | A | 1 | a0001c0002t0018g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41-2050C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152279 | ||||||
chr2:152152363
|
C | T | 1 | a0001c0001t0035g0064 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-2134G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152363 | ||||||
chr2:152152403
|
C | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-2174G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152403 | ||||||
chr2:152152406
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.41-2177C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152406 | ||||||
chr2:152152422
|
G | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.41-2193C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152422 | ||||||
chr2:152152427
|
T | C | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-2198A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152427 | ||||||
chr2:152152474
|
G | A | 1 | a0001c0001t0037g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-2245C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152474 | ||||||
chr2:152152555
|
A | C | 1 | a0001c0001t0038g0211 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41-2326T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152555 | ||||||
chr2:152152561
|
C | CA | 92 | a0001c0001t0003g0017a0001c0001t0003g0180a0001c0001t0003g0181others(89): Show | 98 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.41-2333dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152561 | ||||||
chr2:152152603
|
C | T | 3 | a0001c0001t0012g0162a0001c0001t0053g0097a0001c0001t0054g0098 | 3 | HG02647.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.41-2374G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152603 | ||||||
chr2:152152617
|
A | G | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.41-2388T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152617 | ||||||
chr2:152152895
|
C | T | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.41-2666G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152895 | ||||||
chr2:152152955
|
A | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-2726T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152152955 | ||||||
chr2:152153133
|
CT | C | 2 | a0001c0001t0007g0009a0001c0001t0007g0300 | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-2905delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153133 | ||||||
chr2:152153150
|
A | G | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-2921T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153150 | ||||||
chr2:152153171
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-2942A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153171 | ||||||
chr2:152153271
|
C | G | 1 | a0001c0001t0019g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41-3042G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153271 | ||||||
chr2:152153303
|
T | C | 1 | a0001c0001t0061g0317 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.41-3074A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153303 | ||||||
chr2:152153397
|
A | G | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3168T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153397 | ||||||
chr2:152153406
|
A | T | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-3177T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153406 | ||||||
chr2:152153646
|
A | G | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-3417T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153646 | ||||||
chr2:152153793
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.41-3564A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153793 | ||||||
chr2:152153885
|
T | TAC | 38 | a0001c0001t0001g0007a0001c0001t0001g0270a0001c0001t0001g0271others(35): Show | 42 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.41-3658_41-3657dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
T | TACAC | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(49): Show | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.41-3660_41-3657dup others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
T | TACACAC | 24 | a0001c0001t0001g0024a0001c0001t0001g0134a0001c0001t0001g0139others(21): Show | 26 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.41-3662_41-3657dup others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
T | TACACACA others(1): Show |
13 | a0001c0001t0001g0257a0001c0001t0006g0140a0001c0001t0006g0302others(10): Show | 13 | HG01123.hp2 HG01358.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-3664_41-3657dup others(8): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
T | TACACACA others(3): Show |
3 | a0001c0001t0006g0136a0001c0001t0011g0148a0001c0001t0015g0288 | 3 | HG00280.hp2 HG01106.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.41-3666_41-3657dup others(10): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
TAC | T | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.41-3658_41-3657del others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
TACAC | T | 5 | a0001c0001t0005g0066a0001c0001t0007g0009a0001c0001t0007g0117others(2): Show | 7 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-3660_41-3657del others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153885
|
TACACAC | T | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3662_41-3657del others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153885 | ||||||
chr2:152153911
|
C | CACAA | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-3683_41-3682ins others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153911 | ||||||
chr2:152153919
|
C | T | 1 | a0001c0001t0016g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41-3690G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152153919 | ||||||
chr2:152154214
|
T | C | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-3985A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154214 | ||||||
chr2:152154404
|
A | T | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.41-4175T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154404 | ||||||
chr2:152154479
|
G | A | 14 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0241others(11): Show | 17 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-4250C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154479 | ||||||
chr2:152154601
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 6 | HG00558.hp2 HG00673.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-4372C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154601 | ||||||
chr2:152154618
|
T | TACAAA | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-4394_41-4390dup others(5): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154618 | ||||||
chr2:152154700
|
G | T | 1 | a0001c0001t0001g0269 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.41-4471C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154700 | ||||||
chr2:152154800
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0076a0001c0001t0037g0077 | 3 | HG03017.hp1 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.41-4571G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154800 | ||||||
chr2:152154961
|
TG | T | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-4733delC | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152154961 | ||||||
chr2:152155120
|
C | A | 10 | a0001c0001t0003g0017a0001c0001t0003g0183a0001c0001t0003g0225others(7): Show | 11 | HG00609.hp1 HG03688.hp2 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-4891G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155120 | ||||||
chr2:152155193
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-4964A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155193 | ||||||
chr2:152155616
|
A | G | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.41-5387T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155616 | ||||||
chr2:152155679
|
G | A | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-5450C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152155679 | ||||||
chr2:152156016
|
C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-5787G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156016 | ||||||
chr2:152156092
|
T | A | 6 | a0001c0001t0001g0139a0001c0001t0006g0137a0001c0001t0006g0140others(3): Show | 6 | HG01123.hp2 HG01167.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-5863A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156092 | ||||||
chr2:152156438
|
T | C | 1 | a0001c0001t0024g0227 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.41-6209A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156438 | ||||||
chr2:152156446
|
A | G | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-6217T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156446 | ||||||
chr2:152156483
|
G | A | 1 | a0001c0001t0006g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.41-6254C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156483 | ||||||
chr2:152156496
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0042g0283 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.41-6267C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156496 | ||||||
chr2:152156539
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41-6310C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156539 | ||||||
chr2:152156629
|
A | G | 1 | a0001c0001t0004g0209 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.41-6400T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156629 | ||||||
chr2:152156667
|
T | A | 1 | a0001c0001t0005g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.41-6438A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156667 | ||||||
chr2:152156790
|
C | A | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.41-6561G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156790 | ||||||
chr2:152156918
|
G | A | 1 | a0001c0001t0009g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.41-6689C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152156918 | ||||||
chr2:152157085
|
A | C | 1 | a0001c0001t0003g0301 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-6856T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157085 | ||||||
chr2:152157123
|
T | A | 1 | a0001c0001t0002g0103 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.41-6894A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157123 | ||||||
chr2:152157649
|
T | G | 1 | a0001c0001t0003g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41-7420A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157649 | ||||||
chr2:152157822
|
A | C | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-7593T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157822 | ||||||
chr2:152157889
|
C | G | 1 | a0001c0001t0011g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41-7660G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157889 | ||||||
chr2:152157927
|
A | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.41-7698T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152157927 | ||||||
chr2:152158170
|
T | A | 1 | a0001c0001t0004g0215 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.41-7941A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158170 | ||||||
chr2:152158202
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-7973G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158202 | ||||||
chr2:152158203
|
G | A | 1 | a0001c0001t0008g0311 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.41-7974C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158203 | ||||||
chr2:152158475
|
C | CA | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-8247dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158475 | ||||||
chr2:152158486
|
T | A | 1 | a0001c0001t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-8257A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158486 | ||||||
chr2:152158596
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.41-8367A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158596 | ||||||
chr2:152158690
|
C | T | 1 | a0001c0001t0008g0308 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.41-8461G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158690 | ||||||
chr2:152158773
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-8544A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158773 | ||||||
chr2:152158789
|
T | C | 3 | a0001c0001t0017g0198a0001c0001t0017g0204a0001c0001t0017g0221 | 3 | HG00408.hp2 NA18983.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.41-8560A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158789 | ||||||
chr2:152158836
|
C | G | 3 | a0001c0001t0005g0066a0001c0001t0005g0067a0001c0001t0005g0068 | 3 | HG02015.hp2 HG02071.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41-8607G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152158836 | ||||||
chr2:152159092
|
A | C | 1 | a0001c0001t0008g0316 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.41-8863T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159092 | ||||||
chr2:152159094
|
C | CAT | 45 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(42): Show | 48 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.41-8867_41-8866dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATAT | 3 | a0001c0001t0003g0190a0001c0001t0016g0107a0001c0001t0016g0108 | 3 | HG03225.hp1 HG03942.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.41-8871_41-8866dup others(6): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(9): Show |
2 | a0001c0001t0004g0242a0001c0001t0021g0243 | 2 | NA18968.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.41-8881_41-8866dup others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(11): Show |
1 | a0001c0001t0014g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(15): Show |
1 | a0001c0001t0003g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(17): Show |
4 | a0001c0001t0003g0241a0001c0001t0014g0031a0001c0001t0014g0032others(1): Show | 4 | HG01433.hp1 HG02109.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(19): Show |
5 | a0001c0001t0003g0180a0001c0001t0003g0301a0001c0001t0004g0217others(2): Show | 5 | HG00738.hp2 HG02683.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(21): Show |
24 | a0001c0001t0003g0239a0001c0001t0003g0247a0001c0001t0003g0248others(21): Show | 25 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(23): Show |
19 | a0001c0001t0003g0179a0001c0001t0003g0185a0001c0001t0003g0236others(16): Show | 22 | HG01070.hp2 HG01361.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(25): Show |
9 | a0001c0001t0003g0184a0001c0001t0003g0233a0001c0001t0003g0249others(6): Show | 9 | HG00408.hp2 HG00609.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(32): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(27): Show |
16 | a0001c0001t0003g0017a0001c0001t0003g0230a0001c0001t0003g0231others(13): Show | 17 | HG00639.hp2 HG02015.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(34): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(29): Show |
13 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0220others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(36): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(31): Show |
7 | a0001c0001t0003g0181a0001c0001t0003g0226a0001c0001t0004g0197others(4): Show | 7 | HG01243.hp1 HG02630.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(38): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(33): Show |
4 | a0001c0001t0003g0225a0001c0001t0004g0195a0001c0001t0022g0194others(1): Show | 4 | HG01943.hp1 HG01981.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-8866_41-8865ins others(40): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159094
|
C | CATATATA others(47): Show |
1 | a0001c0001t0004g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.41-8866_41-8865ins others(54): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159094 | ||||||
chr2:152159108
|
T | TATATATA others(19): Show |
1 | a0001c0001t0003g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.41-8880_41-8879ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159108 | ||||||
chr2:152159110
|
T | TATATATA others(9): Show |
5 | a0001c0001t0002g0003a0001c0001t0002g0089a0001c0001t0002g0096others(2): Show | 7 | HG02155.hp2 HG02165.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(16): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(11): Show |
1 | a0001c0001t0002g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(11): Show |
42 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(39): Show | 54 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(18): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(13): Show |
1 | a0001c0001t0002g0091 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(20): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(13): Show |
14 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(11): Show | 14 | HG02015.hp2 HG02071.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(20): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(15): Show |
2 | a0001c0001t0008g0319a0001c0001t0062g0315 | 2 | HG03688.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(15): Show |
14 | a0001c0001t0002g0062a0001c0001t0005g0055a0001c0001t0005g0065others(11): Show | 15 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(22): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(17): Show |
6 | a0001c0001t0002g0095a0001c0001t0005g0104a0001c0001t0008g0312others(3): Show | 6 | HG02027.hp2 HG02698.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(24): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(19): Show |
3 | a0001c0001t0003g0183a0001c0001t0003g0244a0001c0001t0024g0191 | 3 | HG04184.hp2 NA18943.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(21): Show |
2 | a0001c0001t0008g0320a0001c0001t0009g0048 | 2 | HG03139.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(23): Show |
2 | a0001c0001t0016g0029a0001c0001t0051g0041 | 2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(25): Show |
1 | a0001c0001t0009g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(32): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(27): Show |
3 | a0001c0001t0009g0042a0001c0001t0009g0050a0001c0001t0016g0028 | 3 | HG02145.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(34): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(35): Show |
1 | a0001c0001t0009g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(42): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(39): Show |
1 | a0001c0001t0009g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(46): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(35): Show |
2 | a0001c0001t0009g0047a0001c0001t0058g0049 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.41-8882_41-8881ins others(42): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159110
|
T | TATATATA others(39): Show |
1 | a0001c0001t0009g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.41-8882_41-8881ins others(46): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159110 | ||||||
chr2:152159207
|
G | C | 1 | a0001c0001t0006g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-8978C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159207 | ||||||
chr2:152159325
|
A | G | 1 | a0001c0001t0004g0224 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.41-9096T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159325 | ||||||
chr2:152159538
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.41-9309G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159538 | ||||||
chr2:152159577
|
T | G | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-9348A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159577 | ||||||
chr2:152159585
|
G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9356C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159585 | ||||||
chr2:152159735
|
A | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41-9506T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159735 | ||||||
chr2:152159874
|
G | A | 1 | a0001c0001t0024g0191 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41-9645C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159874 | ||||||
chr2:152159876
|
G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9647C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159876 | ||||||
chr2:152159896
|
T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9667A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159896 | ||||||
chr2:152159920
|
G | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-9691C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159920 | ||||||
chr2:152159940
|
G | A | 4 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0254others(1): Show | 4 | HG02683.hp2 HG02738.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9711C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159940 | ||||||
chr2:152159973
|
T | C | 1 | a0001c0001t0041g0284 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.41-9744A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159973 | ||||||
chr2:152159978
|
G | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-9749C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159978 | ||||||
chr2:152159999
|
A | G | 213 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(210): Show | 234 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.41-9770T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152159999 | ||||||
chr2:152160062
|
G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-9833C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160062 | ||||||
chr2:152160070
|
G | A | 4 | a0001c0001t0009g0046a0001c0001t0009g0047a0001c0001t0009g0048others(1): Show | 4 | HG02145.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9841C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160070 | ||||||
chr2:152160098
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.41-9869C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160098 | ||||||
chr2:152160149
|
A | AC | 6 | a0001c0001t0002g0062a0001c0001t0003g0223a0001c0001t0008g0311others(3): Show | 6 | HG00621.hp2 HG01261.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-9921dupG | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160149 | ||||||
chr2:152160157
|
G | A | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-9928C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160157 | ||||||
chr2:152160257
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(61): Show | 78 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.41-10028G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160257 | ||||||
chr2:152160297
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-10068G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160297 | ||||||
chr2:152160325
|
A | G | 1 | a0001c0001t0059g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41-10096T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160325 | ||||||
chr2:152160342
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-10113C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160342 | ||||||
chr2:152160386
|
G | A | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.41-10157C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160386 | ||||||
chr2:152160404
|
G | A | 1 | a0001c0001t0017g0221 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.41-10175C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160404 | ||||||
chr2:152160547
|
G | A | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-10318C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160547 | ||||||
chr2:152160614
|
C | T | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41-10385G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160614 | ||||||
chr2:152160648
|
G | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(63): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.41-10419C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160648 | ||||||
chr2:152160652
|
G | A | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.41-10423C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160652 | ||||||
chr2:152160655
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.41-10426C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160655 | ||||||
chr2:152160670
|
G | A | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.41-10441C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160670 | ||||||
chr2:152160682
|
C | T | 1 | a0001c0001t0006g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-10453G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160682 | ||||||
chr2:152160683
|
G | A | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-10454C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160683 | ||||||
chr2:152160686
|
C | T | 89 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-10457G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160686 | ||||||
chr2:152160687
|
G | A | 1 | a0001c0001t0061g0317 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.41-10458C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160687 | ||||||
chr2:152160710
|
C | G | 2 | a0001c0001t0007g0117a0001c0001t0057g0118 | 2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.41-10481G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160710 | ||||||
chr2:152160726
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10497A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160726 | ||||||
chr2:152160736
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.41-10507C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160736 | ||||||
chr2:152160749
|
T | C | 260 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0266others(257): Show | 284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.41-10520A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160749 | ||||||
chr2:152160759
|
C | T | 4 | a0001c0002t0018g0153a0001c0002t0018g0155a0001c0002t0018g0156others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-10530G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160759 | ||||||
chr2:152160760
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10531C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160760 | ||||||
chr2:152160772
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10543G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160772 | ||||||
chr2:152160772
|
CGGGAAGT others(169): Show |
C | 1 | a0001c0001t0004g0253 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.41-10719_41-10544d others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160772 | ||||||
chr2:152160799
|
C | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.41-10570G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160799 | ||||||
chr2:152160841
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.41-10612G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160841 | ||||||
chr2:152160846
|
G | A | 88 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(85): Show | 94 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.41-10617C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160846 | ||||||
chr2:152160904
|
C | A | 1 | a0001c0001t0002g0096 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.41-10675G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160904 | ||||||
chr2:152160908
|
A | ATCCGGGA others(169): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.41-10680_41-10679i others(178): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160908 | ||||||
chr2:152160908
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-10679T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160908 | ||||||
chr2:152160936
|
A | G | 89 | a0001c0001t0002g0061a0001c0001t0003g0017a0001c0001t0003g0179others(86): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.41-10707T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152160936 | ||||||
chr2:152161031
|
C | T | 2 | a0001c0001t0003g0190a0001c0001t0003g0249 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.41-10802G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161031 | ||||||
chr2:152161056
|
G | C | 9 | a0001c0001t0003g0190a0001c0001t0003g0249a0001c0001t0011g0142others(6): Show | 9 | HG01192.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-10827C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161056 | ||||||
chr2:152161059
|
G | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-10830C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161059 | ||||||
chr2:152161087
|
C | T | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | NA18981.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.41-10858G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161087 | ||||||
chr2:152161099
|
G | A | 1 | a0001c0001t0015g0286 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.41-10870C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161099 | ||||||
chr2:152161260
|
G | A | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.41-11031C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161260 | ||||||
chr2:152161278
|
T | C | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.41-11049A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161278 | ||||||
chr2:152161307
|
G | C | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.41-11078C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161307 | ||||||
chr2:152161440
|
T | C | 1 | a0001c0001t0046g0246 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.41-11211A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161440 | ||||||
chr2:152161494
|
TA | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.41-11266delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161494 | ||||||
chr2:152161494
|
TAA | T | 32 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0012g0161others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.41-11267_41-11266d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161494 | ||||||
chr2:152161507
|
A | C | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.41-11278T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161507 | ||||||
chr2:152161512
|
A | C | 2 | a0001c0001t0002g0099a0001c0001t0032g0105 | 2 | HG00280.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.41-11283T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161512 | ||||||
chr2:152161689
|
A | G | 1 | a0001c0001t0023g0192 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.41-11460T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152161689 | ||||||
chr2:152162450
|
C | T | 1 | a0001c0001t0024g0191 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41-12221G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162450 | ||||||
chr2:152162506
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(54): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.41-12277C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162506 | ||||||
chr2:152162786
|
G | A | 2 | a0001c0001t0044g0163a0001c0001t0047g0178 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.41-12557C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162786 | ||||||
chr2:152162789
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.41-12560G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162789 | ||||||
chr2:152162807
|
A | AT | 236 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(233): Show | 259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.41-12579dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162807 | ||||||
chr2:152162807
|
A | ATT | 12 | a0001c0001t0005g0055a0001c0001t0008g0027a0001c0001t0008g0316others(9): Show | 13 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.41-12580_41-12579d others(4): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162807 | ||||||
chr2:152162810
|
T | TC | 6 | a0001c0001t0012g0165a0001c0001t0012g0166a0001c0001t0012g0167others(3): Show | 6 | HG00639.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-12582_41-12581i others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162810 | ||||||
chr2:152162913
|
G | C | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-12684C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162913 | ||||||
chr2:152162921
|
A | T | 11 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(8): Show | 11 | HG00639.hp1 HG01070.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+12682T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162921 | ||||||
chr2:152162953
|
C | T | 12 | a0001c0001t0007g0009a0001c0001t0007g0040a0001c0001t0007g0117others(9): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+12650G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162953 | ||||||
chr2:152162983
|
A | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+12620T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152162983 | ||||||
chr2:152163061
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.40+12542T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163061 | ||||||
chr2:152163200
|
G | A | 1 | a0001c0001t0055g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.40+12403C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163200 | ||||||
chr2:152163251
|
A | C | 2 | a0001c0001t0008g0309a0001c0001t0008g0310 | 2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.40+12352T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163251 | ||||||
chr2:152163350
|
C | G | 11 | a0001c0001t0008g0027a0001c0001t0008g0316a0001c0001t0008g0318others(8): Show | 12 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+12253G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163350 | ||||||
chr2:152163399
|
C | T | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+12204G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163399 | ||||||
chr2:152163487
|
T | TAAG | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.40+12115_40+12116i others(5): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163487 | ||||||
chr2:152163610
|
G | T | 94 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(91): Show | 101 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.40+11993C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163610 | ||||||
chr2:152163732
|
A | C | 24 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(21): Show | 25 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.40+11871T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163732 | ||||||
chr2:152163743
|
C | G | 1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40+11860G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152163743 | ||||||
chr2:152164031
|
T | C | 3 | a0001c0001t0019g0172a0001c0001t0020g0173a0001c0001t0020g0174 | 3 | HG02257.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.40+11572A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164031 | ||||||
chr2:152164098
|
A | G | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.40+11505T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164098 | ||||||
chr2:152164125
|
G | A | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+11478C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164125 | ||||||
chr2:152164139
|
T | C | 1 | a0001c0001t0040g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.40+11464A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164139 | ||||||
chr2:152164219
|
A | G | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG00609.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.40+11384T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164219 | ||||||
chr2:152164570
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.40+11033C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164570 | ||||||
chr2:152164693
|
C | T | 95 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(92): Show | 109 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.40+10910G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164693 | ||||||
chr2:152164753
|
A | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.40+10850T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164753 | ||||||
chr2:152164795
|
T | C | 1 | a0001c0001t0043g0289 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.40+10808A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164795 | ||||||
chr2:152164804
|
C | T | 3 | a0001c0001t0001g0115a0001c0001t0015g0113a0001c0001t0015g0114 | 3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.40+10799G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164804 | ||||||
chr2:152164912
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.40+10691A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164912 | ||||||
chr2:152164917
|
C | G | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.40+10686G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152164917 | ||||||
chr2:152165024
|
C | A | 2 | a0001c0001t0006g0149a0001c0001t0006g0150 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.40+10579G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165024 | ||||||
chr2:152165056
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.40+10547G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165056 | ||||||
chr2:152165075
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.40+10528A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165075 | ||||||
chr2:152165169
|
C | T | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+10434G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165169 | ||||||
chr2:152165261
|
T | TA | 7 | a0001c0001t0001g0292a0001c0001t0014g0031a0001c0001t0014g0032others(4): Show | 7 | HG01167.hp2 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+10341dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165261 | ||||||
chr2:152165355
|
C | A | 3 | a0001c0001t0001g0115a0001c0001t0015g0113a0001c0001t0015g0114 | 3 | HG02055.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.40+10248G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165355 | ||||||
chr2:152165469
|
A | G | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+10134T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165469 | ||||||
chr2:152165557
|
C | T | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+10046G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165557 | ||||||
chr2:152165842
|
T | C | 3 | a0001c0001t0007g0122a0001c0001t0007g0123a0001c0001t0007g0124 | 3 | HG02109.hp1 HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.40+9761A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165842 | ||||||
chr2:152165869
|
C | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+9734G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165869 | ||||||
chr2:152165924
|
C | T | 1 | a0001c0001t0059g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.40+9679G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165924 | ||||||
chr2:152165959
|
G | T | 82 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(79): Show | 88 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.40+9644C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165959 | ||||||
chr2:152165977
|
C | T | 1 | a0001c0001t0008g0308 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.40+9626G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152165977 | ||||||
chr2:152166005
|
C | T | 1 | a0001c0001t0051g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+9598G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166005 | ||||||
chr2:152166065
|
T | C | 2 | a0001c0001t0053g0097a0001c0001t0054g0098 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.40+9538A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166065 | ||||||
chr2:152166085
|
C | A | 1 | a0001c0001t0045g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+9518G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166085 | ||||||
chr2:152166091
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+9512A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166091 | ||||||
chr2:152166166
|
T | A | 3 | a0001c0001t0019g0157a0001c0001t0019g0158a0001c0001t0045g0159 | 3 | HG02258.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.40+9437A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166166 | ||||||
chr2:152166176
|
AAAC | A | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.40+9424_40+9426del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166176 | ||||||
chr2:152166375
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.40+9228C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166375 | ||||||
chr2:152166492
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.40+9111G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166492 | ||||||
chr2:152166646
|
G | C | 257 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(254): Show | 281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.40+8957C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166646 | ||||||
chr2:152166829
|
C | A | 1 | a0001c0001t0008g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.40+8774G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152166829 | ||||||
chr2:152167085
|
TTCA | T | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+8515_40+8517del others(3): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167085 | ||||||
chr2:152167111
|
T | A | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+8492A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167111 | ||||||
chr2:152167236
|
T | G | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+8367A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167236 | ||||||
chr2:152167459
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.40+8144C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167459 | ||||||
chr2:152167508
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+8095A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167508 | ||||||
chr2:152167599
|
G | A | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.40+8004C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167599 | ||||||
chr2:152167670
|
G | C | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+7933C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167670 | ||||||
chr2:152167731
|
G | GA | 173 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(170): Show | 191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.40+7871dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167731 | ||||||
chr2:152167735
|
A | AT | 84 | a0001c0001t0002g0051a0001c0001t0003g0017a0001c0001t0003g0179others(81): Show | 90 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.40+7867_40+7868ins others(1): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167735 | ||||||
chr2:152167739
|
T | A | 8 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(5): Show | 8 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.40+7864A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167739 | ||||||
chr2:152167921
|
A | AAAAAT | 3 | a0001c0001t0004g0186a0001c0001t0004g0187a0001c0001t0004g0188 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+7677_40+7681dup others(5): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152167921 | ||||||
chr2:152168163
|
AT | A | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+7439delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168163 | ||||||
chr2:152168171
|
T | G | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+7432A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168171 | ||||||
chr2:152168286
|
G | A | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+7317C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168286 | ||||||
chr2:152168401
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+7202C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168401 | ||||||
chr2:152168448
|
G | A | 1 | a0001c0001t0013g0025 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.40+7155C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168448 | ||||||
chr2:152168449
|
C | T | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+7154G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168449 | ||||||
chr2:152168516
|
G | C | 81 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(78): Show | 87 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.40+7087C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168516 | ||||||
chr2:152168591
|
C | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(78): Show | 96 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.40+7012G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168591 | ||||||
chr2:152168829
|
C | T | 7 | a0001c0001t0019g0157a0001c0001t0019g0158a0001c0001t0045g0159others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+6774G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168829 | ||||||
chr2:152168905
|
C | A | 1 | a0001c0001t0058g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.40+6698G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168905 | ||||||
chr2:152168973
|
T | A | 2 | a0001c0001t0013g0293a0001c0001t0013g0298 | 2 | HG01074.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.40+6630A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152168973 | ||||||
chr2:152169064
|
T | C | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+6539A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169064 | ||||||
chr2:152169151
|
G | C | 316 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.40+6452C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169151 | ||||||
chr2:152169246
|
T | C | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+6357A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169246 | ||||||
chr2:152169275
|
C | A | 1 | a0001c0001t0013g0294 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.40+6328G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169275 | ||||||
chr2:152169337
|
T | C | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(316): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.40+6266A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169337 | ||||||
chr2:152169423
|
C | A | 1 | a0001c0001t0009g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.40+6180G>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169423 | ||||||
chr2:152169593
|
A | C | 1 | a0001c0002t0018g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+6010T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169593 | ||||||
chr2:152169856
|
C | CT | 63 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(60): Show | 77 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.40+5746dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169856 | ||||||
chr2:152169856
|
CT | C | 9 | a0001c0001t0001g0295a0001c0001t0006g0306a0001c0001t0007g0116others(6): Show | 9 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+5746delA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169856 | ||||||
chr2:152169910
|
G | A | 1 | a0001c0001t0011g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.40+5693C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152169910 | ||||||
chr2:152170028
|
C | G | 316 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.40+5575G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170028 | ||||||
chr2:152170115
|
G | A | 1 | a0001c0001t0008g0320 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.40+5488C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170115 | ||||||
chr2:152170356
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+5247C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170356 | ||||||
chr2:152170444
|
C | T | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+5159G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170444 | ||||||
chr2:152170482
|
CA | C | 188 | a0001c0001t0001g0260a0001c0001t0002g0001a0001c0001t0002g0003others(185): Show | 209 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.40+5120delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170482 | ||||||
chr2:152170601
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.40+5002C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170601 | ||||||
chr2:152170680
|
A | C | 1 | a0001c0001t0056g0154 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.40+4923T>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170680 | ||||||
chr2:152170799
|
T | C | 1 | a0001c0001t0032g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.40+4804A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170799 | ||||||
chr2:152170937
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+4666T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152170937 | ||||||
chr2:152171090
|
T | C | 1 | a0001c0001t0019g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40+4513A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171090 | ||||||
chr2:152171114
|
T | C | 2 | a0001c0001t0006g0149a0001c0001t0006g0150 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.40+4489A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171114 | ||||||
chr2:152171151
|
C | T | 1 | a0001c0002t0018g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.40+4452G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171151 | ||||||
chr2:152171260
|
T | G | 1 | a0001c0001t0007g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40+4343A>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171260 | ||||||
chr2:152171425
|
C | CTT | 258 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0002g0001others(255): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.40+4176_40+4177dup others(2): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171425 | ||||||
chr2:152171633
|
T | C | 1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.40+3970A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171633 | ||||||
chr2:152171891
|
G | C | 1 | a0001c0001t0007g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.40+3712C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171891 | ||||||
chr2:152171960
|
G | T | 11 | a0001c0001t0009g0038a0001c0001t0009g0042a0001c0001t0009g0043others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.40+3643C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152171960 | ||||||
chr2:152172553
|
G | A | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+3050C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172553 | ||||||
chr2:152172577
|
G | T | 7 | a0001c0001t0001g0260a0001c0001t0014g0031a0001c0001t0014g0032others(4): Show | 7 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+3026C>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172577 | ||||||
chr2:152172578
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.40+3025C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172578 | ||||||
chr2:152172611
|
G | A | 12 | a0001c0001t0007g0009a0001c0001t0007g0040a0001c0001t0007g0117others(9): Show | 14 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+2992C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172611 | ||||||
chr2:152172632
|
G | A | 5 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+2971C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172632 | ||||||
chr2:152172682
|
A | G | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+2921T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172682 | ||||||
chr2:152172747
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.40+2856A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172747 | ||||||
chr2:152172796
|
G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0012others(97): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.40+2807C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172796 | ||||||
chr2:152172862
|
C | CA | 6 | a0001c0001t0016g0028a0001c0001t0016g0029a0001c0001t0016g0106others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+2740dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172862 | ||||||
chr2:152172862
|
CA | C | 6 | a0001c0001t0001g0259a0001c0001t0001g0296a0001c0001t0003g0184others(3): Show | 6 | HG01168.hp2 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2740delT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172862 | ||||||
chr2:152172874
|
A | G | 1 | a0001c0001t0003g0183 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.40+2729T>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152172874 | ||||||
chr2:152173207
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.40+2396C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173207 | ||||||
chr2:152173210
|
C | CA | 6 | a0001c0001t0001g0297a0001c0001t0002g0128a0001c0001t0003g0252others(3): Show | 6 | HG01074.hp1 HG01074.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2392dupT | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173210 | ||||||
chr2:152173355
|
T | C | 2 | a0001c0001t0006g0151a0001c0001t0006g0152 | 2 | NA18957.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.40+2248A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173355 | ||||||
chr2:152173361
|
C | CACATATA others(23): Show |
2 | a0001c0001t0003g0181a0001c0001t0047g0178 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.40+2212_40+2241dup others(30): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | ||||||
chr2:152173361
|
C | CACATATA others(51): Show |
1 | a0001c0001t0050g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.40+2241_40+2242ins others(58): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | ||||||
chr2:152173361
|
C | CACATATA others(21): Show |
77 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0183others(74): Show | 83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.40+2241_40+2242ins others(28): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | ||||||
chr2:152173361
|
C | CACATATA others(51): Show |
1 | a0001c0001t0003g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.40+2241_40+2242ins others(58): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173361 | ||||||
chr2:152173365
|
T | C | 31 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0006g0026others(28): Show | 32 | HG00140.hp2 HG00733.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.40+2238A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173365 | ||||||
chr2:152173375
|
T | TATATATA others(19): Show |
1 | a0001c0001t0003g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.40+2227_40+2228ins others(26): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173375 | ||||||
chr2:152173395
|
T | C | 24 | a0001c0001t0012g0161a0001c0001t0012g0162a0001c0001t0012g0165others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+2208A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173395 | ||||||
chr2:152173404
|
A | AT | 6 | a0001c0001t0014g0031a0001c0001t0014g0032a0001c0001t0014g0033others(3): Show | 6 | HG01167.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+2198dupA | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173404 | ||||||
chr2:152173404
|
A | T | 1 | a0001c0001t0003g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.40+2199T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173404 | ||||||
chr2:152173406
|
A | ACGTATAT others(93): Show |
1 | a0001c0001t0028g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40+2196_40+2197ins others(100): Show |
STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173406 | ||||||
chr2:152173406
|
A | T | 189 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(186): Show | 209 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.40+2197T>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173406 | ||||||
chr2:152173408
|
T | A | 1 | a0001c0004t0018g0176 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.40+2195A>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173408 | ||||||
chr2:152173543
|
C | T | 1 | a0001c0001t0009g0030 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+2060G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173543 | ||||||
chr2:152173555
|
C | T | 1 | a0001c0001t0013g0255 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2048G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173555 | ||||||
chr2:152173751
|
T | C | 1 | a0001c0001t0006g0177 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.40+1852A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173751 | ||||||
chr2:152173776
|
C | G | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1827G>C | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152173776 | ||||||
chr2:152174076
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.40+1527C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174076 | ||||||
chr2:152174243
|
C | T | 1 | a0001c0001t0047g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.40+1360G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174243 | ||||||
chr2:152174355
|
G | A | 83 | a0001c0001t0003g0017a0001c0001t0003g0179a0001c0001t0003g0180others(80): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+1248C>T | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174355 | ||||||
chr2:152174599
|
T | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(54): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.40+1004A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174599 | ||||||
chr2:152174879
|
T | C | 2 | a0001c0001t0007g0009a0001c0001t0007g0300 | 4 | HG02922.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+724A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174879 | ||||||
chr2:152174920
|
G | C | 1 | a0001c0001t0003g0301 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40+683C>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174920 | ||||||
chr2:152174957
|
T | C | 6 | a0001c0001t0006g0026a0001c0001t0006g0302a0001c0001t0006g0303others(3): Show | 7 | HG01081.hp2 HG01358.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+646A>G | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152174957 | ||||||
chr2:152175488
|
C | T | 2 | a0001c0001t0016g0028a0001c0001t0016g0029 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.40+115G>A | STAM2 | ENSG00000115145.10 | transcript | ENST00000263904.5 | protein_coding | 1/13 | chr2 | 152175488 |