geneid | 8936 |
---|---|
ensemblid | ENSG00000112290.13 |
hgncid | 12732 |
symbol | WASF1 |
name | WASP family member 1 |
refseq_nuc | NM_003931.3 |
refseq_prot | NP_003922.1 |
ensembl_nuc | ENST00000392589.6 |
ensembl_prot | ENSP00000376368.1 |
mane_status | MANE Select |
chr | chr6 |
start | 110099819 |
end | 110179670 |
strand | - |
ver | v1.2 |
region | chr6:110099819-110179670 |
region5000 | chr6:110094819-110184670 |
regionname0 | WASF1_chr6_110099819_110179670 |
regionname5000 | WASF1_chr6_110094819_110184670 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 259 | 81 | 46 | 98 | 8 | 24 | 78 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0002 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0003 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0004 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1680 | 239 | 69 | 40 | 98 | 7 | 23 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0002 | 0/0 | 1680 | 18 | 10 | 6 | 0 | 1 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0003 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0004 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0006 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1207 | 99 | 18 | 24 | 39 | 3 | 14 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0002 | 0/0 | 1207 | 64 | 19 | 16 | 25 | 1 | 3 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0003 | 1/0 | 1207 | 45 | 20 | 6 | 15 | 1 | 2 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0004 | 0/0 | 1207 | 32 | 7 | 0 | 20 | 2 | 3 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0005 | 0/0 | 1206 | 8 | 8 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0006 | 0/0 | 1207 | 6 | 6 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0007 | 0/0 | 1207 | 2 | 2 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0008 | 0/0 | 1207 | 2 | 0 | 0 | 0 | 0 | 2 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0009 | 0/0 | 1207 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0010 | 0/0 | 1207 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0011 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
t0012 | 0/0 | 1207 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1680 | 239 | 69 | 40 | 98 | 7 | 23 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0002 | 0/0 | 1680 | 18 | 10 | 6 | 0 | 1 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0003 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0006 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0002c0007 | 0/0 | 1680 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0003c0005 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0004c0004 | 0/0 | 1680 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2886 | 97 | 16 | 24 | 39 | 3 | 14 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0002 | 0/0 | 2886 | 45 | 9 | 10 | 24 | 0 | 2 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0003 | 1/0 | 2886 | 44 | 20 | 6 | 14 | 1 | 2 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0004 | 0/0 | 2886 | 32 | 7 | 0 | 20 | 2 | 3 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0005 | 0/0 | 2885 | 8 | 8 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0006 | 0/0 | 2886 | 6 | 6 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0007 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0008 | 0/0 | 2886 | 2 | 0 | 0 | 0 | 0 | 2 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0009 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0010 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0001t0012 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0002t0002 | 0/0 | 2886 | 18 | 10 | 6 | 0 | 1 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0003t0011 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0001c0006t0001 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0002c0007t0001 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0003c0005t0003 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
a0004c0004t0002 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | copy fasta | chr6 | 110094819 | 110184670 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0003t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0001c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0002c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0003c0005t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
a0004c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0002 | g0194 | EUR | FIN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00280 | hp2 | a0001 | c0001 | t0010 | g0138 | EUR | FIN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0150 | EUR | IBS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02145 | hp2 | a0002 | c0007 | t0001 | g0047 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CDX | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0205 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0262 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ESN | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03453 | hp1 | a0001 | c0003 | t0011 | g0220 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0158 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0208 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0228 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG04204 | hp2 | a0001 | c0001 | t0008 | g0227 | SAS | STU | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18953 | hp2 | a0003 | c0005 | t0003 | g0098 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18983 | hp2 | a0004 | c0004 | t0002 | g0254 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0122 | EUR | TSI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | GIH | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | MSL | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | USA | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | USA | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | USA | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | LWK | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0055 | REF | REF | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0049 | REF | REF | WASF1_chr6_110094819_110184670 | WASF1 | chr6 | 110094819 | 110184670 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110100668
|
G | A | 1 | a0004 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Cys | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 2037/2886 | 1534/1680 | 512/559 | chr6 | 110100668 | ||
chr6:110102178
|
G | A | 1 | a0003 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.932C>T | p.Pro311Leu | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 10/11 | 1435/2886 | 932/1680 | 311/559 | chr6 | 110102178 | ||
chr6:110108637
|
T | C | 1 | a0002 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.313A>G | p.Thr105Ala | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/11 | 816/2886 | 313/1680 | 105/559 | chr6 | 110108637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110100615
|
G | A | 1 | a0001c0003 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1587C>T | p.Asn529Asn | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 2090/2886 | 1587/1680 | 529/559 | chr6 | 110100615 | ||
chr6:110105412
|
T | C | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.708A>G | p.Glu236Glu | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/11 | 1211/2886 | 708/1680 | 236/559 | chr6 | 110105412 | ||
chr6:110127539
|
G | A | 1 | a0001c0002 | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
synonymous_variant | LOW | c.63C>T | p.Gly21Gly | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/11 | 566/2886 | 63/1680 | 21/559 | chr6 | 110127539 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110099925
|
C | T | 1 | a0001c0001t0006 | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 597 | chr6 | 110099925 | |||||
chr6:110099929
|
T | C | 1 | a0001c0003t0011 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 593 | chr6 | 110099929 | |||||
chr6:110100026
|
GA | G | 1 | a0001c0001t0005 | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*495delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 495 | chr6 | 110100026 | |||||
chr6:110100074
|
T | C | 1 | a0001c0001t0009 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 448 | chr6 | 110100074 | |||||
chr6:110100158
|
C | T | 13 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | 214 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*364G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 11/11 | 364 | chr6 | 110100158 | |||||
chr6:110178602
|
T | A | 1 | a0001c0001t0010 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/11 | 51001 | chr6 | 110178602 | |||||
chr6:110178622
|
T | C | 1 | a0001c0001t0007 | 2 | HG06807.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-151A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/11 | 51021 | chr6 | 110178622 | |||||
chr6:110179455
|
C | T | 1 | a0001c0001t0004 | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-288G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/11 | 51854 | chr6 | 110179455 | |||||
chr6:110179521
|
G | A | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(5): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
5_prime_UTR_variant | MODIFIER | c.-354C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/11 | 51920 | chr6 | 110179521 | |||||
chr6:110179618
|
C | A | 1 | a0001c0001t0012 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-451G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/11 | 52017 | chr6 | 110179618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:110100731
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1523-52T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 10/10 | chr6 | 110100731 | ||||||
chr6:110100996
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1523-317T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 10/10 | chr6 | 110100996 | ||||||
chr6:110101399
|
C | G | 39 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(36): Show | 39 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1522+189G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 10/10 | chr6 | 110101399 | ||||||
chr6:110102295
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.894-79A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102295 | ||||||
chr6:110102320
|
G | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.894-104C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102320 | ||||||
chr6:110102353
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(7): Show | 10 | HG01081.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.894-137T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102353 | ||||||
chr6:110102425
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02630.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-209C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102425 | ||||||
chr6:110102509
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.894-293T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102509 | ||||||
chr6:110102734
|
A | AGAAAATT others(321): Show |
4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-519_894-518ins others(328): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102734 | ||||||
chr6:110102735
|
G | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894-519C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102735 | ||||||
chr6:110102860
|
T | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.893+518A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110102860 | ||||||
chr6:110103138
|
T | C | 75 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0024others(72): Show | 75 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.893+240A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110103138 | ||||||
chr6:110103141
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.893+237A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 9/10 | chr6 | 110103141 | ||||||
chr6:110103560
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.714-3T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110103560 | ||||||
chr6:110103791
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.714-234A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110103791 | ||||||
chr6:110103795
|
A | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.714-238T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110103795 | ||||||
chr6:110103796
|
T | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.714-239A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110103796 | ||||||
chr6:110104009
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.714-452G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104009 | ||||||
chr6:110104042
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.714-485G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104042 | ||||||
chr6:110104137
|
C | T | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.714-580G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104137 | ||||||
chr6:110104295
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.714-738G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104295 | ||||||
chr6:110104317
|
GAAAT | G | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.714-764_714-761del others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104317 | ||||||
chr6:110104330
|
A | G | 1 | a0001c0001t0004g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.714-773T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104330 | ||||||
chr6:110104638
|
A | T | 4 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0160others(1): Show | 4 | NA18977.hp1 NA19063.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.713+769T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104638 | ||||||
chr6:110104843
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.713+564A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104843 | ||||||
chr6:110104902
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.713+505T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110104902 | ||||||
chr6:110105076
|
C | T | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.713+331G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110105076 | ||||||
chr6:110105166
|
C | T | 1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.713+241G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110105166 | ||||||
chr6:110105183
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.713+224G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110105183 | ||||||
chr6:110105295
|
T | C | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.713+112A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 8/10 | chr6 | 110105295 | ||||||
chr6:110105954
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | NA18955.hp1 NA18971.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-375C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110105954 | ||||||
chr6:110106142
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-563C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106142 | ||||||
chr6:110106258
|
G | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02135.hp2 HG02273.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.541-679C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106258 | ||||||
chr6:110106379
|
A | C | 1 | a0001c0001t0002g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.540+698T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106379 | ||||||
chr6:110106404
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.540+673C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106404 | ||||||
chr6:110106431
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.540+646C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106431 | ||||||
chr6:110106650
|
T | C | 23 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0154others(20): Show | 23 | HG00673.hp1 HG02027.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.540+427A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106650 | ||||||
chr6:110106680
|
C | T | 1 | a0001c0001t0002g0243 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.540+397G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106680 | ||||||
chr6:110106843
|
C | T | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+234G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 7/10 | chr6 | 110106843 | ||||||
chr6:110107250
|
T | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.423-56A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107250 | ||||||
chr6:110107321
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.423-127A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107321 | ||||||
chr6:110107476
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.423-282T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107476 | ||||||
chr6:110107589
|
G | T | 5 | a0001c0001t0004g0155a0001c0001t0004g0159a0001c0001t0004g0161others(2): Show | 5 | HG02027.hp2 HG02165.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-395C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107589 | ||||||
chr6:110107594
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.423-400T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107594 | ||||||
chr6:110107627
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.423-433C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107627 | ||||||
chr6:110107644
|
A | T | 1 | a0001c0001t0002g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.423-450T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107644 | ||||||
chr6:110107734
|
C | T | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-540G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107734 | ||||||
chr6:110107777
|
A | G | 1 | a0001c0002t0002g0196 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.423-583T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107777 | ||||||
chr6:110107817
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.423-623A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107817 | ||||||
chr6:110107851
|
A | C | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.423-657T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107851 | ||||||
chr6:110107938
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.422+590C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107938 | ||||||
chr6:110107964
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.422+564G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107964 | ||||||
chr6:110107989
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.422+539G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110107989 | ||||||
chr6:110108013
|
T | C | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.422+515A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108013 | ||||||
chr6:110108102
|
G | A | 2 | a0001c0001t0003g0058a0001c0001t0003g0127 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.422+426C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108102 | ||||||
chr6:110108137
|
C | CA | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.422+390dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108137 | ||||||
chr6:110108137
|
C | CAA | 60 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0032others(57): Show | 60 | HG00673.hp1 HG00738.hp1 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.422+389_422+390dup others(2): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108137 | ||||||
chr6:110108137
|
C | CAAA | 8 | a0001c0001t0004g0160a0001c0001t0004g0173a0001c0001t0004g0174others(5): Show | 8 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.422+388_422+390dup others(3): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108137 | ||||||
chr6:110108161
|
AG | A | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.422+366delC | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108161 | ||||||
chr6:110108162
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422+366C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108162 | ||||||
chr6:110108306
|
A | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.422+222T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108306 | ||||||
chr6:110108385
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18968.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.422+143C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108385 | ||||||
chr6:110108417
|
G | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.422+111C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 6/10 | chr6 | 110108417 | ||||||
chr6:110109175
|
TAAAAC | T | 10 | a0001c0001t0003g0019a0001c0001t0003g0023a0001c0001t0003g0041others(7): Show | 10 | HG00408.hp1 HG02083.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-499_269-495del others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109175 | ||||||
chr6:110109408
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.269-727G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109408 | ||||||
chr6:110109414
|
A | G | 14 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246others(11): Show | 14 | HG00408.hp2 HG00639.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-733T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109414 | ||||||
chr6:110109440
|
C | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.269-759G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109440 | ||||||
chr6:110109470
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.269-789A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109470 | ||||||
chr6:110109528
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.269-847C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109528 | ||||||
chr6:110109552
|
C | CT | 7 | a0001c0001t0001g0054a0001c0001t0003g0027a0001c0001t0003g0085others(4): Show | 7 | HG01516.hp1 HG01517.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-872dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109552 | ||||||
chr6:110109552
|
CT | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.269-872delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109552 | ||||||
chr6:110109615
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.269-934C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109615 | ||||||
chr6:110109708
|
T | C | 2 | a0001c0001t0004g0170a0001c0001t0004g0172 | 2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.269-1027A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109708 | ||||||
chr6:110109713
|
G | A | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-1032C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109713 | ||||||
chr6:110109733
|
TA | T | 4 | a0001c0001t0002g0231a0001c0001t0004g0151a0001c0001t0004g0162others(1): Show | 4 | HG01168.hp2 HG01516.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-1053delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109733 | ||||||
chr6:110109734
|
A | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 119 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.269-1053T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109734 | ||||||
chr6:110109755
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.269-1074C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109755 | ||||||
chr6:110109858
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.269-1177G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110109858 | ||||||
chr6:110110095
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.269-1414C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110095 | ||||||
chr6:110110106
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.269-1425C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110106 | ||||||
chr6:110110587
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.269-1906A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110587 | ||||||
chr6:110110820
|
G | GT | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-2140dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110820 | ||||||
chr6:110110895
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.269-2214T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110895 | ||||||
chr6:110110915
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.269-2234C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110915 | ||||||
chr6:110110948
|
T | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-2267A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110110948 | ||||||
chr6:110111078
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.268+2248A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111078 | ||||||
chr6:110111108
|
A | G | 1 | a0001c0001t0010g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.268+2218T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111108 | ||||||
chr6:110111270
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.268+2056G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111270 | ||||||
chr6:110111315
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.268+2011A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111315 | ||||||
chr6:110111685
|
T | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.268+1641A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111685 | ||||||
chr6:110111916
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.268+1410C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110111916 | ||||||
chr6:110112071
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.268+1255G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112071 | ||||||
chr6:110112227
|
T | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+1099A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112227 | ||||||
chr6:110112381
|
G | A | 113 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0002g0190others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.268+945C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112381 | ||||||
chr6:110112575
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+751G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112575 | ||||||
chr6:110112667
|
C | T | 41 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.268+659G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112667 | ||||||
chr6:110112798
|
G | T | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.268+528C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112798 | ||||||
chr6:110112849
|
G | A | 9 | a0001c0001t0001g0057a0001c0001t0005g0181a0001c0001t0005g0182others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+477C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112849 | ||||||
chr6:110112894
|
C | CA | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.268+431dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112894 | ||||||
chr6:110112894
|
C | CAA | 6 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0002g0209others(3): Show | 6 | HG01074.hp2 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+430_268+431dup others(2): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112894 | ||||||
chr6:110112898
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0004g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.268+416_268+427del others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112898 | ||||||
chr6:110112899
|
AAAAAAAA others(4): Show |
A | 36 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(33): Show | 36 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(33): Show |
intron_variant | MODIFIER | c.268+416_268+426del others(11): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112899 | ||||||
chr6:110112900
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0160a0001c0001t0004g0162a0001c0001t0004g0167 | 3 | NA18939.hp1 NA18977.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.268+416_268+425del others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112900 | ||||||
chr6:110112905
|
A | C | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.268+421T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112905 | ||||||
chr6:110112909
|
A | AAAC | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+416_268+417ins others(3): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112909 | ||||||
chr6:110112909
|
A | AAC | 10 | a0001c0002t0002g0199a0001c0002t0002g0200a0001c0002t0002g0201others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+416_268+417ins others(2): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112909 | ||||||
chr6:110112910
|
C | A | 19 | a0001c0001t0001g0139a0001c0002t0002g0191a0001c0002t0002g0192others(16): Show | 19 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.268+416G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110112910 | ||||||
chr6:110113150
|
C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+176G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110113150 | ||||||
chr6:110113155
|
G | A | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.268+171C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110113155 | ||||||
chr6:110113252
|
C | T | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.268+74G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 5/10 | chr6 | 110113252 | ||||||
chr6:110113604
|
A | G | 1 | a0001c0001t0004g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.134-144T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110113604 | ||||||
chr6:110113663
|
C | T | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.134-203G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110113663 | ||||||
chr6:110113873
|
A | AATCT | 113 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0002g0190others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.134-414_134-413ins others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110113873 | ||||||
chr6:110113970
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.134-510T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110113970 | ||||||
chr6:110113993
|
T | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-533A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110113993 | ||||||
chr6:110114149
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.134-689G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110114149 | ||||||
chr6:110114303
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.134-843C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110114303 | ||||||
chr6:110114369
|
G | A | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-909C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110114369 | ||||||
chr6:110114533
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1073G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110114533 | ||||||
chr6:110114702
|
T | C | 41 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.134-1242A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110114702 | ||||||
chr6:110115122
|
C | A | 29 | a0001c0001t0002g0240a0001c0001t0004g0149a0001c0001t0004g0150others(26): Show | 29 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.134-1662G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115122 | ||||||
chr6:110115181
|
T | G | 1 | a0001c0001t0005g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.134-1721A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115181 | ||||||
chr6:110115205
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.134-1745A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115205 | ||||||
chr6:110115209
|
G | GA | 7 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 7 | HG01943.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-1750dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115209 | ||||||
chr6:110115501
|
T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.134-2041A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115501 | ||||||
chr6:110115593
|
C | A | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-2133G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115593 | ||||||
chr6:110115665
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.134-2205C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110115665 | ||||||
chr6:110116171
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 260 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.134-2711T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116171 | ||||||
chr6:110116335
|
A | T | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.134-2875T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116335 | ||||||
chr6:110116461
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.134-3001G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116461 | ||||||
chr6:110116552
|
C | CAGTAAGG | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-3099_134-3093d others(9): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116552 | ||||||
chr6:110116563
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG01081.hp2 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-3103T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116563 | ||||||
chr6:110116581
|
A | G | 1 | a0001c0001t0001g0055 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.134-3121T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116581 | ||||||
chr6:110116729
|
G | A | 24 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0154others(21): Show | 24 | HG00673.hp1 HG02027.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.134-3269C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116729 | ||||||
chr6:110116777
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.134-3317G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110116777 | ||||||
chr6:110117039
|
C | G | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-3579G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117039 | ||||||
chr6:110117079
|
GA | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 119 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.134-3620delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117079 | ||||||
chr6:110117159
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-3699C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117159 | ||||||
chr6:110117438
|
A | T | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.134-3978T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117438 | ||||||
chr6:110117504
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.134-4044T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117504 | ||||||
chr6:110117923
|
A | G | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-4463T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117923 | ||||||
chr6:110117982
|
A | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.134-4522T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117982 | ||||||
chr6:110117995
|
C | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02273.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.134-4535G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110117995 | ||||||
chr6:110118277
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.134-4817C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118277 | ||||||
chr6:110118332
|
C | CAAGCAAA others(4): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(2): Show | 5 | HG01074.hp2 HG02572.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-4883_134-4873d others(13): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118332 | ||||||
chr6:110118347
|
C | CA | 7 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0066others(4): Show | 7 | HG01074.hp1 HG01346.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-4888dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
C | CAAACGGA others(5): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0016 | 2 | HG03579.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.134-4888_134-4887i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
CA | C | 95 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0028others(92): Show | 95 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.134-4888delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
CAA | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 23 | HG00733.hp2 HG01169.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-4889_134-4888d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
CAAA | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0068a0001c0001t0002g0211others(36): Show | 39 | HG00673.hp1 HG00741.hp2 HG02071.hp1 others(36): Show |
intron_variant | MODIFIER | c.134-4890_134-4888d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
CAAAA | C | 34 | a0001c0001t0001g0081a0001c0001t0002g0219a0001c0001t0002g0221others(31): Show | 34 | HG00408.hp2 HG00639.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.134-4891_134-4888d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118347
|
CAAAAA | C | 9 | a0001c0001t0002g0225a0001c0001t0002g0245a0001c0001t0005g0181others(6): Show | 9 | HG01257.hp1 HG02559.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-4892_134-4888d others(7): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118347 | ||||||
chr6:110118380
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.134-4920G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118380 | ||||||
chr6:110118475
|
A | T | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134-5015T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118475 | ||||||
chr6:110118593
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.134-5133G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118593 | ||||||
chr6:110118708
|
C | T | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5248G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118708 | ||||||
chr6:110118789
|
T | TG | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.134-5330dupC | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110118789 | ||||||
chr6:110119024
|
T | C | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.134-5564A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119024 | ||||||
chr6:110119073
|
T | C | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.134-5613A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119073 | ||||||
chr6:110119181
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.134-5721C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119181 | ||||||
chr6:110119223
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-5763G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119223 | ||||||
chr6:110119238
|
A | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-5778T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119238 | ||||||
chr6:110119612
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.134-6152T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119612 | ||||||
chr6:110119699
|
C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-6239G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119699 | ||||||
chr6:110119913
|
C | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.134-6453G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119913 | ||||||
chr6:110119961
|
G | T | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.134-6501C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110119961 | ||||||
chr6:110120206
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.134-6746T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120206 | ||||||
chr6:110120261
|
C | G | 1 | a0001c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.134-6801G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120261 | ||||||
chr6:110120273
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.134-6813A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120273 | ||||||
chr6:110120336
|
G | A | 1 | a0001c0002t0002g0195 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.134-6876C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120336 | ||||||
chr6:110120337
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134-6877G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120337 | ||||||
chr6:110120590
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+6879G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120590 | ||||||
chr6:110120636
|
T | C | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.133+6833A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120636 | ||||||
chr6:110120763
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | NA18955.hp1 NA18971.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+6706T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120763 | ||||||
chr6:110120787
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+6682G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120787 | ||||||
chr6:110120986
|
G | C | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.133+6483C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110120986 | ||||||
chr6:110121061
|
T | C | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.133+6408A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121061 | ||||||
chr6:110121135
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.133+6334A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121135 | ||||||
chr6:110121305
|
T | A | 1 | a0001c0001t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.133+6164A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121305 | ||||||
chr6:110121527
|
G | A | 39 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0223others(36): Show | 39 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.133+5942C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121527 | ||||||
chr6:110121902
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+5567C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121902 | ||||||
chr6:110121935
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.133+5534A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110121935 | ||||||
chr6:110122182
|
C | A | 38 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(35): Show | 38 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+5287G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122182 | ||||||
chr6:110122191
|
TAAGA | T | 21 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0211others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+5274_133+5277d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122191 | ||||||
chr6:110122239
|
C | CA | 57 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0211others(54): Show | 57 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.133+5229dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122239 | ||||||
chr6:110122239
|
C | CAAA | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+5227_133+5229d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122239 | ||||||
chr6:110122261
|
TAGA | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+5205_133+5207d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122261 | ||||||
chr6:110122292
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.133+5177T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122292 | ||||||
chr6:110122312
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+5157G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122312 | ||||||
chr6:110122472
|
G | T | 29 | a0001c0001t0004g0176a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.133+4997C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122472 | ||||||
chr6:110122482
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0003g0085a0001c0001t0005g0181others(25): Show | 28 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.133+4987T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122482 | ||||||
chr6:110122496
|
C | T | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.133+4973G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122496 | ||||||
chr6:110122537
|
T | A | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+4932A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122537 | ||||||
chr6:110122545
|
C | T | 1 | a0003c0005t0003g0098 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.133+4924G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122545 | ||||||
chr6:110122603
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.133+4866G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122603 | ||||||
chr6:110122649
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.133+4820A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122649 | ||||||
chr6:110122700
|
T | C | 1 | a0001c0001t0003g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.133+4769A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122700 | ||||||
chr6:110122711
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+4758A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122711 | ||||||
chr6:110122822
|
G | T | 1 | a0001c0003t0011g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133+4647C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122822 | ||||||
chr6:110122837
|
T | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+4632A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122837 | ||||||
chr6:110122955
|
G | A | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.133+4514C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110122955 | ||||||
chr6:110123060
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.133+4409G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123060 | ||||||
chr6:110123077
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.133+4392C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123077 | ||||||
chr6:110123087
|
A | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+4382T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123087 | ||||||
chr6:110123100
|
G | C | 43 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(40): Show | 43 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.133+4369C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123100 | ||||||
chr6:110123270
|
AGG | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0107a0001c0001t0001g0114others(5): Show | 8 | HG00735.hp2 HG01168.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.133+4197_133+4198d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123270 | ||||||
chr6:110123330
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.133+4139G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123330 | ||||||
chr6:110123432
|
C | T | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+4037G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123432 | ||||||
chr6:110123502
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+3967T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110123502 | ||||||
chr6:110124182
|
CCCATCAG others(3): Show |
C | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.133+3277_133+3286d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124182 | ||||||
chr6:110124190
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3279G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124190 | ||||||
chr6:110124191
|
G | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3278C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124191 | ||||||
chr6:110124191
|
G | GTC | 4 | a0001c0001t0001g0075a0001c0001t0001g0111a0001c0001t0001g0137others(1): Show | 4 | NA18968.hp1 NA18989.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3276_133+3277d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124191 | ||||||
chr6:110124191
|
G | GTCTC | 5 | a0001c0001t0002g0237a0001c0001t0006g0212a0001c0001t0006g0215others(2): Show | 5 | HG01346.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+3274_133+3277d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124191 | ||||||
chr6:110124192
|
T | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3277A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124192 | ||||||
chr6:110124193
|
C | G | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3276G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124193 | ||||||
chr6:110124194
|
TCTCTCTC others(34): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.133+3234_133+3274d others(43): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124194 | ||||||
chr6:110124196
|
TCTCTCTC others(32): Show |
T | 2 | a0001c0001t0001g0004a0001c0001t0007g0017 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.133+3234_133+3272d others(41): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124196 | ||||||
chr6:110124200
|
T | TCCTCTCT others(48): Show |
1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+3268_133+3269i others(57): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124200 | ||||||
chr6:110124202
|
TCTCTCTC others(26): Show |
T | 1 | a0001c0001t0007g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133+3234_133+3266d others(35): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124202 | ||||||
chr6:110124204
|
TCTCTCTC others(24): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133+3234_133+3264d others(33): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124204 | ||||||
chr6:110124208
|
T | TCTCTCTC others(4): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0094 | 2 | NA18959.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.133+3260_133+3261i others(13): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124208 | ||||||
chr6:110124212
|
TCTCTC | T | 6 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0253others(3): Show | 6 | HG02897.hp1 HG03017.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3252_133+3256d others(7): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124212 | ||||||
chr6:110124212
|
TCTCTCCT others(7): Show |
T | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133+3243_133+3256d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124212 | ||||||
chr6:110124214
|
TCTC | T | 19 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(16): Show | 19 | HG00639.hp1 HG00741.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.133+3252_133+3254d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124214 | ||||||
chr6:110124215
|
C | CCTCCCTC others(3): Show |
1 | a0001c0002t0002g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.133+3253_133+3254i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124215 | ||||||
chr6:110124216
|
T | C | 1 | a0001c0002t0002g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.133+3253A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124216 | ||||||
chr6:110124216
|
TC | T | 21 | a0001c0001t0002g0190a0001c0001t0002g0232a0001c0001t0002g0235others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+3252delG | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124216 | ||||||
chr6:110124216
|
TCCTCTCT others(12): Show |
T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3234_133+3252d others(21): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124216 | ||||||
chr6:110124217
|
C | CT | 34 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0233others(31): Show | 34 | HG00673.hp1 HG02055.hp2 HG02132.hp2 others(31): Show |
intron_variant | MODIFIER | c.133+3251_133+3252i others(3): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCC others(3): Show |
3 | a0001c0001t0002g0231a0001c0001t0002g0238a0001c0003t0011g0220 | 3 | HG03453.hp1 NA18951.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.133+3251_133+3252i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCC others(5): Show |
1 | a0001c0001t0002g0239 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.133+3251_133+3252i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCT | 4 | a0001c0001t0002g0226a0001c0001t0004g0154a0001c0001t0004g0163others(1): Show | 4 | NA19009.hp2 NA19067.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+3251_133+3252i others(9): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCT others(2): Show |
4 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0159others(1): Show | 4 | HG02027.hp2 HG02165.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+3251_133+3252i others(11): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCT others(4): Show |
4 | a0001c0001t0004g0156a0001c0001t0004g0157a0001c0001t0004g0162others(1): Show | 4 | HG02132.hp1 HG03579.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3251_133+3252i others(13): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124217
|
C | CTCTCTCT others(6): Show |
1 | a0001c0001t0004g0155 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.133+3251_133+3252i others(15): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124217 | ||||||
chr6:110124219
|
T | C | 1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133+3250A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124219 | ||||||
chr6:110124221
|
T | C | 1 | a0001c0002t0002g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.133+3248A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124221 | ||||||
chr6:110124223
|
T | C | 12 | a0001c0001t0002g0190a0001c0002t0002g0191a0001c0002t0002g0193others(9): Show | 12 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3246A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124223 | ||||||
chr6:110124224
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0004g0158 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.133+3244_133+3245i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124224 | ||||||
chr6:110124224
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0004g0160 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.133+3244_133+3245i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124224 | ||||||
chr6:110124224
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0004g0169 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.133+3244_133+3245i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124224 | ||||||
chr6:110124224
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0004g0173 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.133+3244_133+3245i others(38): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124224 | ||||||
chr6:110124224
|
C | T | 12 | a0001c0001t0002g0190a0001c0002t0002g0191a0001c0002t0002g0193others(9): Show | 12 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3245G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124224 | ||||||
chr6:110124225
|
T | C | 13 | a0001c0001t0002g0190a0001c0001t0006g0214a0001c0002t0002g0191others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+3244A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124225 | ||||||
chr6:110124225
|
TC | T | 13 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0245others(10): Show | 13 | HG00408.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.133+3243delG | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124225 | ||||||
chr6:110124226
|
C | CT | 48 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(45): Show | 48 | HG00673.hp1 HG01257.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.133+3242_133+3243i others(3): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124226 | ||||||
chr6:110124226
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.133+3243G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124226 | ||||||
chr6:110124227
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.133+3242G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124227 | ||||||
chr6:110124228
|
T | C | 2 | a0001c0001t0002g0257a0001c0002t0002g0198 | 2 | HG01346.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.133+3241A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124228 | ||||||
chr6:110124230
|
T | C | 1 | a0001c0002t0002g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.133+3239A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124230 | ||||||
chr6:110124232
|
T | C | 3 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0005g0188 | 3 | HG01516.hp1 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.133+3237A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124232 | ||||||
chr6:110124233
|
C | CTCTCTCT others(15): Show |
1 | a0001c0001t0004g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.133+3235_133+3236i others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124233 | ||||||
chr6:110124233
|
C | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.133+3236G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124233 | ||||||
chr6:110124233
|
CT | C | 3 | a0001c0002t0002g0193a0001c0002t0002g0199a0001c0002t0002g0205 | 3 | HG01168.hp2 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.133+3235delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124233 | ||||||
chr6:110124234
|
T | C | 14 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(11): Show | 14 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.133+3235A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124234 | ||||||
chr6:110124234
|
TC | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG00408.hp2 HG00639.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.133+3234delG | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124234 | ||||||
chr6:110124235
|
C | CCT | 8 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0051others(5): Show | 8 | HG00741.hp1 HG01106.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.133+3232_133+3233d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCT | 4 | a0001c0001t0001g0055a0001c0001t0003g0026a0001c0001t0003g0119others(1): Show | 4 | HG02145.hp1 HG03471.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3230_133+3233d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCT | 5 | a0001c0001t0001g0050a0001c0001t0001g0069a0001c0001t0003g0052others(2): Show | 5 | HG01175.hp2 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3228_133+3233d others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(1): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0059others(3): Show | 6 | HG01358.hp1 HG02135.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3226_133+3233d others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(16): Show |
1 | a0001c0001t0001g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.133+3233_133+3234i others(25): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(24): Show |
2 | a0001c0001t0003g0123a0001c0001t0012g0262 | 2 | HG03130.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.133+3233_133+3234i others(33): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(3): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0001g0090others(6): Show | 9 | HG00408.hp1 HG01978.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+3224_133+3233d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(5): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0070others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3222_133+3233d others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(7): Show |
3 | a0001c0001t0001g0034a0001c0001t0001g0078a0001c0001t0009g0077 | 3 | HG02486.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.133+3220_133+3233d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(9): Show |
3 | a0001c0001t0001g0022a0001c0001t0003g0019a0001c0001t0003g0101 | 3 | HG01928.hp1 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.133+3218_133+3233d others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTCTCTC others(11): Show |
2 | a0001c0001t0001g0093a0001c0001t0003g0040 | 2 | HG02129.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133+3216_133+3233d others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTTCCTC others(1): Show |
5 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0155others(2): Show | 5 | HG02027.hp2 HG03579.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3233_133+3234i others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CCTTCCTC others(3): Show |
3 | a0001c0001t0004g0154a0001c0001t0004g0156a0001c0001t0004g0161 | 3 | HG02132.hp1 HG02165.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.133+3233_133+3234i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CT | 43 | a0001c0001t0001g0111a0001c0001t0002g0219a0001c0001t0002g0221others(40): Show | 43 | HG00733.hp2 HG00741.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.133+3233_133+3234i others(3): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0004g0167 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.133+3233_133+3234i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0004g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.133+3233_133+3234i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CTCTCTCT others(21): Show |
2 | a0001c0001t0004g0170a0001c0001t0004g0171 | 2 | NA18964.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.133+3233_133+3234i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CTCTCTCT others(23): Show |
4 | a0001c0001t0004g0168a0001c0001t0004g0172a0001c0001t0004g0174others(1): Show | 4 | HG02738.hp2 NA18950.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+3233_133+3234i others(32): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0004g0164 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133+3233_133+3234i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124235
|
C | T | 2 | a0001c0001t0002g0241a0001c0002t0002g0191 | 2 | HG01106.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.133+3234G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124235 | ||||||
chr6:110124236
|
CT | C | 3 | a0001c0001t0004g0160a0001c0001t0004g0169a0001c0001t0004g0173 | 3 | NA18977.hp1 NA18989.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.133+3232delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124236 | ||||||
chr6:110124237
|
T | C | 1 | a0001c0001t0005g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133+3232A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124237 | ||||||
chr6:110124239
|
T | C | 15 | a0001c0001t0002g0189a0001c0001t0002g0209a0001c0001t0002g0210others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+3230A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124239 | ||||||
chr6:110124241
|
T | C | 7 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0155others(4): Show | 7 | HG00673.hp1 HG02027.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+3228A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124241 | ||||||
chr6:110124243
|
T | C | 1 | a0001c0001t0004g0163 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.133+3226A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124243 | ||||||
chr6:110124243
|
T | TCTCCTCT others(3): Show |
1 | a0001c0001t0001g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.133+3225_133+3226i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124243 | ||||||
chr6:110124245
|
T | C | 1 | a0001c0001t0004g0165 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.133+3224A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124245 | ||||||
chr6:110124247
|
T | C | 1 | a0001c0001t0004g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133+3222A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124247 | ||||||
chr6:110124252
|
C | A | 4 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246others(1): Show | 4 | NA18953.hp1 NA18979.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+3217G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124252 | ||||||
chr6:110124254
|
C | A | 6 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(3): Show | 6 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+3215G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124254 | ||||||
chr6:110124256
|
C | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0232a0001c0001t0002g0244others(5): Show | 8 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+3213G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124256 | ||||||
chr6:110124258
|
C | A | 7 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(4): Show | 7 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+3211G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124258 | ||||||
chr6:110124260
|
C | A | 7 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(4): Show | 7 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+3209G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124260 | ||||||
chr6:110124262
|
C | A | 7 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(4): Show | 7 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+3207G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124262 | ||||||
chr6:110124264
|
C | A | 7 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(4): Show | 7 | HG02559.hp2 NA18953.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+3205G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124264 | ||||||
chr6:110124266
|
C | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(5): Show | 8 | HG02451.hp2 HG02559.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+3203G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124266 | ||||||
chr6:110124266
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0002g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.133+3189_133+3202d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124266 | ||||||
chr6:110124268
|
C | A | 8 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(5): Show | 8 | HG02451.hp2 HG02559.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+3201G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124268 | ||||||
chr6:110124268
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0002g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.133+3200_133+3201i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124268 | ||||||
chr6:110124268
|
CTCTCTCT others(3): Show |
C | 1 | a0001c0001t0003g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.133+3191_133+3200d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124268 | ||||||
chr6:110124268
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.133+3187_133+3200d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124268 | ||||||
chr6:110124270
|
C | A | 13 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0097others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.133+3199G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124270 | ||||||
chr6:110124270
|
C | CTATATAT others(15): Show |
1 | a0001c0001t0002g0249 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133+3198_133+3199i others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124270 | ||||||
chr6:110124270
|
C | CTATATAT others(21): Show |
1 | a0001c0001t0002g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.133+3198_133+3199i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124270 | ||||||
chr6:110124270
|
CTCTCTAT others(9): Show |
C | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133+3183_133+3198d others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124270 | ||||||
chr6:110124270
|
CTCTCTAT others(15): Show |
C | 1 | a0001c0001t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.133+3177_133+3198d others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124270 | ||||||
chr6:110124272
|
C | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0073others(18): Show | 21 | HG00408.hp2 HG01516.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.133+3197G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATA | 3 | a0001c0001t0001g0016a0001c0001t0001g0146a0001c0001t0005g0188 | 3 | HG02523.hp2 HG02559.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.133+3196_133+3197i others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0094a0001c0001t0002g0222 | 2 | HG00741.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.133+3196_133+3197i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133+3196_133+3197i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0002g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.133+3196_133+3197i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(11): Show |
1 | a0001c0001t0002g0237 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.133+3196_133+3197i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0002g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.133+3196_133+3197i others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
C | CTATATAT others(19): Show |
1 | a0001c0002t0002g0205 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133+3196_133+3197i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124272
|
CTCTATAT others(7): Show |
C | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.133+3183_133+3196d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124272 | ||||||
chr6:110124274
|
C | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(39): Show | 42 | HG00408.hp2 HG00741.hp2 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.133+3195G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATA | 5 | a0001c0001t0002g0225a0001c0001t0004g0162a0001c0001t0004g0165others(2): Show | 5 | HG01257.hp1 HG02615.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+3191_133+3194d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATA | 5 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0072others(2): Show | 5 | HG00733.hp1 HG03579.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3189_133+3194d others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0061a0001c0001t0001g0111a0001c0001t0003g0027others(1): Show | 4 | HG03490.hp1 NA19009.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3187_133+3194d others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(3): Show |
6 | a0001c0001t0001g0048a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG00673.hp2 HG01516.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+3185_133+3194d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(5): Show |
3 | a0001c0001t0002g0226a0001c0001t0002g0239a0001c0001t0004g0149 | 3 | NA18959.hp1 NA19009.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.133+3183_133+3194d others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0002g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.133+3181_133+3194d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(9): Show |
1 | a0001c0002t0002g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.133+3179_133+3194d others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(15): Show |
1 | a0001c0001t0004g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133+3173_133+3194d others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(17): Show |
2 | a0001c0001t0002g0258a0001c0001t0005g0182 | 2 | HG01943.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.133+3171_133+3194d others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0002g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.133+3169_133+3194d others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTATATAT others(25): Show |
2 | a0001c0001t0002g0252a0001c0001t0008g0228 | 2 | HG03654.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.133+3163_133+3194d others(34): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTA | 3 | a0001c0001t0003g0131a0001c0001t0006g0216a0002c0007t0001g0047 | 3 | HG02145.hp2 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTATAT others(1): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0092 | 3 | HG02165.hp1 HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTATAT others(5): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0074 | 2 | HG02258.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTATAT others(7): Show |
1 | a0001c0001t0001g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTATAT others(9): Show |
1 | a0001c0001t0001g0075 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(3): Show |
2 | a0001c0001t0001g0096a0001c0001t0003g0120 | 2 | HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(7): Show |
1 | a0001c0001t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(11): Show |
2 | a0001c0001t0001g0056a0001c0001t0002g0241 | 2 | HG00738.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(15): Show |
2 | a0001c0001t0002g0233a0001c0001t0002g0248 | 2 | HG01993.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(19): Show |
1 | a0001c0001t0005g0181 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTAT others(23): Show |
2 | a0001c0001t0002g0236a0001c0002t0002g0199 | 2 | HG02135.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(32): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(1): Show |
3 | a0001c0001t0001g0079a0001c0001t0003g0041a0001c0001t0003g0058 | 3 | HG01891.hp1 HG02129.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(3): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0137a0001c0001t0003g0023 | 3 | NA18957.hp1 NA18968.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0012a0001c0006t0001g0014 | 2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0003g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0004g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(22): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0002g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(27): Show |
2 | a0001c0001t0001g0010a0001c0001t0005g0186 | 2 | HG01074.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(55): Show |
1 | a0001c0001t0005g0187 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(64): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(3): Show |
3 | a0001c0001t0001g0108a0001c0001t0001g0128a0001c0001t0003g0141 | 3 | HG01928.hp2 HG02293.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(5): Show |
1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0105 | 2 | HG00735.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0044 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0063 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0005g0185a0001c0002t0002g0203 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0008g0227 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(38): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0020 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0002g0232 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0005g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(23): Show |
1 | a0001c0002t0002g0204 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(32): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(33): Show |
1 | a0001c0001t0004g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(42): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18968.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(9): Show |
1 | a0001c0001t0001g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(18): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(11): Show |
2 | a0001c0001t0001g0145a0001c0001t0003g0088 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0045a0001c0001t0005g0183 | 2 | HG03486.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.133+3194_133+3195i others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0002g0243 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(27): Show |
1 | a0001c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(36): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(38): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0002g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(40): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0004g0179 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(38): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0004g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(40): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(41): Show |
1 | a0001c0001t0002g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(50): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(38): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(23): Show |
1 | a0001c0001t0002g0242 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(32): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0002g0234 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.133+3194_133+3195i others(40): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.133+3194_133+3195i others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
CTATATA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0117a0001c0001t0002g0255others(2): Show | 5 | HG00639.hp1 HG02486.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3189_133+3194d others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124274
|
CTATATAT others(5): Show |
C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+3183_133+3194d others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124274 | ||||||
chr6:110124276
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(70): Show | 73 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.133+3193T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124276 | ||||||
chr6:110124278
|
A | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0024others(46): Show | 49 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.133+3191T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124278 | ||||||
chr6:110124280
|
A | C | 26 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0059others(23): Show | 26 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.133+3189T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124280 | ||||||
chr6:110124282
|
A | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0107others(12): Show | 15 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+3187T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124282 | ||||||
chr6:110124284
|
A | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0116others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3185T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124284 | ||||||
chr6:110124286
|
A | C | 3 | a0001c0001t0001g0116a0001c0001t0002g0255a0001c0001t0003g0123 | 3 | HG00639.hp1 HG01517.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.133+3183T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124286 | ||||||
chr6:110124288
|
A | C | 1 | a0001c0001t0002g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.133+3181T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124288 | ||||||
chr6:110124368
|
G | T | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.133+3101C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124368 | ||||||
chr6:110124447
|
G | A | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.133+3022C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124447 | ||||||
chr6:110124678
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133+2791C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124678 | ||||||
chr6:110124681
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.133+2788A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124681 | ||||||
chr6:110124803
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.133+2666A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124803 | ||||||
chr6:110124960
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0002g0218a0001c0001t0006g0212others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+2509A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110124960 | ||||||
chr6:110125105
|
T | G | 114 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0002g0190others(111): Show | 114 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2364A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110125105 | ||||||
chr6:110125106
|
T | A | 114 | a0001c0001t0001g0008a0001c0001t0002g0189a0001c0001t0002g0190others(111): Show | 114 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2363A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110125106 | ||||||
chr6:110125235
|
C | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 245 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.133+2234G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110125235 | ||||||
chr6:110125261
|
T | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.133+2208A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110125261 | ||||||
chr6:110126440
|
G | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.133+1029C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110126440 | ||||||
chr6:110126460
|
C | T | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+1009G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110126460 | ||||||
chr6:110126873
|
T | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+596A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110126873 | ||||||
chr6:110126965
|
T | A | 1 | a0001c0001t0003g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+504A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110126965 | ||||||
chr6:110126966
|
C | A | 1 | a0001c0001t0003g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+503G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110126966 | ||||||
chr6:110127093
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133+376C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110127093 | ||||||
chr6:110127198
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+271A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110127198 | ||||||
chr6:110127263
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+206G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110127263 | ||||||
chr6:110127414
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.133+55G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110127414 | ||||||
chr6:110127415
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.133+54C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 4/10 | chr6 | 110127415 | ||||||
chr6:110127635
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18957.hp2 | splice_region_variant&intron_variant | LOW | c.-28-6C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110127635 | ||||||
chr6:110127692
|
T | G | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-63A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110127692 | ||||||
chr6:110127760
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-28-131T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110127760 | ||||||
chr6:110127786
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-157G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110127786 | ||||||
chr6:110127961
|
T | C | 1 | a0001c0003t0011g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-332A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110127961 | ||||||
chr6:110128329
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28-700C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128329 | ||||||
chr6:110128367
|
C | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-738G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128367 | ||||||
chr6:110128447
|
C | G | 1 | a0001c0001t0003g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-28-818G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128447 | ||||||
chr6:110128530
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-901T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128530 | ||||||
chr6:110128578
|
G | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-949C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128578 | ||||||
chr6:110128591
|
T | C | 1 | a0001c0001t0003g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-28-962A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128591 | ||||||
chr6:110128745
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-28-1116G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128745 | ||||||
chr6:110128788
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-1159C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128788 | ||||||
chr6:110128956
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-28-1327G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128956 | ||||||
chr6:110128966
|
G | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-1337C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128966 | ||||||
chr6:110128996
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-28-1367T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110128996 | ||||||
chr6:110129100
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-1471G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129100 | ||||||
chr6:110129424
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-28-1795A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129424 | ||||||
chr6:110129455
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-1826G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129455 | ||||||
chr6:110129507
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-1878C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129507 | ||||||
chr6:110129525
|
C | G | 1 | a0001c0001t0002g0222 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-28-1896G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129525 | ||||||
chr6:110129547
|
T | A | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-1918A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129547 | ||||||
chr6:110129570
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-1941T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129570 | ||||||
chr6:110129592
|
T | TAAAATGT others(327): Show |
1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-1964_-28-1963i others(336): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129592 | ||||||
chr6:110129592
|
T | TAAAATGT others(330): Show |
1 | a0001c0001t0002g0209 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-28-1964_-28-1963i others(339): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129592 | ||||||
chr6:110129592
|
T | TAAAATGT others(331): Show |
2 | a0001c0001t0002g0210a0001c0001t0002g0259 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-28-1964_-28-1963i others(340): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129592 | ||||||
chr6:110129597
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-28-1968G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129597 | ||||||
chr6:110129667
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-28-2038A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129667 | ||||||
chr6:110129701
|
G | C | 20 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28-2072C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129701 | ||||||
chr6:110129720
|
T | A | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-2091A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129720 | ||||||
chr6:110129722
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-28-2093T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129722 | ||||||
chr6:110129822
|
T | G | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-28-2193A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129822 | ||||||
chr6:110129943
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-28-2314A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110129943 | ||||||
chr6:110130215
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-2586T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130215 | ||||||
chr6:110130238
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28-2609T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130238 | ||||||
chr6:110130278
|
G | T | 6 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0084others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-2649C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130278 | ||||||
chr6:110130300
|
A | C | 1 | a0001c0001t0003g0102 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-28-2671T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130300 | ||||||
chr6:110130793
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-3164C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130793 | ||||||
chr6:110130917
|
TTTTAA | T | 41 | a0001c0001t0001g0111a0001c0001t0004g0149a0001c0001t0004g0150others(38): Show | 41 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28-3293_-28-3289d others(7): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130917 | ||||||
chr6:110130926
|
G | A | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28-3297C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110130926 | ||||||
chr6:110131161
|
G | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-3532C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131161 | ||||||
chr6:110131307
|
G | A | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-3678C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131307 | ||||||
chr6:110131700
|
G | T | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-4071C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131700 | ||||||
chr6:110131743
|
T | C | 1 | a0001c0001t0003g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-28-4114A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131743 | ||||||
chr6:110131946
|
C | T | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-28-4317G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131946 | ||||||
chr6:110131974
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-4345A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110131974 | ||||||
chr6:110132110
|
A | T | 3 | a0001c0001t0003g0091a0001c0001t0003g0140a0003c0005t0003g0098 | 3 | NA18953.hp2 NA18969.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-28-4481T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132110 | ||||||
chr6:110132216
|
A | G | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-28-4587T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132216 | ||||||
chr6:110132220
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-4591A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132220 | ||||||
chr6:110132390
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-28-4761A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132390 | ||||||
chr6:110132463
|
G | A | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.-28-4834C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132463 | ||||||
chr6:110132475
|
G | GT | 9 | a0001c0001t0001g0105a0001c0001t0001g0143a0001c0001t0002g0242others(6): Show | 9 | HG01081.hp1 HG02622.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-4847dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132475 | ||||||
chr6:110132517
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-28-4888C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132517 | ||||||
chr6:110132681
|
T | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-5052A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132681 | ||||||
chr6:110132700
|
TC | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-5072delG | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132700 | ||||||
chr6:110132739
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-5110A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132739 | ||||||
chr6:110132821
|
G | A | 1 | a0001c0002t0002g0195 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-28-5192C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132821 | ||||||
chr6:110132963
|
T | TAC | 16 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0056others(13): Show | 16 | HG00408.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-28-5336_-28-5335d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132963 | ||||||
chr6:110132963
|
T | TACAC | 8 | a0001c0001t0001g0090a0001c0001t0001g0145a0001c0001t0002g0259others(5): Show | 8 | HG01891.hp2 HG02083.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-5338_-28-5335d others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132963 | ||||||
chr6:110132963
|
T | TACACACA others(3): Show |
11 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(8): Show | 11 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-5344_-28-5335d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132963 | ||||||
chr6:110132963
|
T | TACACACA others(5): Show |
26 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(23): Show | 26 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-28-5346_-28-5335d others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132963 | ||||||
chr6:110132963
|
T | TACACACA others(7): Show |
1 | a0001c0001t0004g0162 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-28-5348_-28-5335d others(16): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110132963 | ||||||
chr6:110133044
|
TG | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-5416delC | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133044 | ||||||
chr6:110133071
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-28-5442A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133071 | ||||||
chr6:110133309
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0113 | 3 | HG00741.hp1 HG01258.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-28-5680A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133309 | ||||||
chr6:110133311
|
C | T | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-5682G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133311 | ||||||
chr6:110133318
|
C | CT | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-5690dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133318 | ||||||
chr6:110133350
|
C | CT | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-5722dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133350 | ||||||
chr6:110133512
|
T | G | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-5883A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133512 | ||||||
chr6:110133601
|
T | A | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-28-5972A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133601 | ||||||
chr6:110133644
|
G | T | 4 | a0001c0001t0001g0090a0001c0001t0003g0086a0001c0001t0003g0089others(1): Show | 4 | HG02523.hp1 NA18962.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-6015C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133644 | ||||||
chr6:110133737
|
T | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-6108A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133737 | ||||||
chr6:110133824
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-6195C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133824 | ||||||
chr6:110133943
|
T | C | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-6314A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110133943 | ||||||
chr6:110134116
|
T | C | 71 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(68): Show | 71 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-28-6487A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134116 | ||||||
chr6:110134280
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-6651A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134280 | ||||||
chr6:110134377
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-6748T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134377 | ||||||
chr6:110134381
|
T | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-6752A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134381 | ||||||
chr6:110134422
|
C | CTT | 36 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0154others(33): Show | 36 | HG00673.hp1 HG02027.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.-28-6795_-28-6794d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134422 | ||||||
chr6:110134422
|
CT | C | 44 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(41): Show | 44 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-6794delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134422 | ||||||
chr6:110134423
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-6794A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134423 | ||||||
chr6:110134456
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18968.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-28-6827G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134456 | ||||||
chr6:110134488
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-6859C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134488 | ||||||
chr6:110134527
|
T | C | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-28-6898A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134527 | ||||||
chr6:110134549
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-6920A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134549 | ||||||
chr6:110134985
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-7356A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110134985 | ||||||
chr6:110135168
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-28-7539C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135168 | ||||||
chr6:110135180
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-7551A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135180 | ||||||
chr6:110135201
|
T | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-7572A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135201 | ||||||
chr6:110135215
|
A | C | 1 | a0001c0002t0002g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-28-7586T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135215 | ||||||
chr6:110135320
|
C | CA | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-7692dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135320 | ||||||
chr6:110135459
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-28-7830G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135459 | ||||||
chr6:110135606
|
G | T | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28-7977C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135606 | ||||||
chr6:110135721
|
C | CT | 49 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG00408.hp1 HG00673.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.-28-8093dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135721 | ||||||
chr6:110135721
|
C | CTTT | 5 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0215others(2): Show | 5 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-8095_-28-8093d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135721 | ||||||
chr6:110135721
|
CT | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0001g0060others(8): Show | 11 | HG01943.hp2 HG02273.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-8093delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135721 | ||||||
chr6:110135747
|
A | T | 16 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(13): Show | 16 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-28-8118T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135747 | ||||||
chr6:110135748
|
C | A | 18 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-28-8119G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135748 | ||||||
chr6:110135787
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-28-8158C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135787 | ||||||
chr6:110135876
|
C | CT | 21 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0092others(18): Show | 21 | HG00280.hp1 HG01106.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-28-8248dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135876 | ||||||
chr6:110135876
|
CT | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(60): Show | 63 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-28-8248delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135876 | ||||||
chr6:110135876
|
CTT | C | 38 | a0001c0001t0002g0189a0001c0001t0002g0223a0001c0001t0002g0245others(35): Show | 38 | HG00673.hp1 HG01243.hp1 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.-28-8249_-28-8248d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135876 | ||||||
chr6:110135876
|
CTTT | C | 6 | a0001c0001t0002g0210a0001c0001t0002g0218a0001c0001t0004g0149others(3): Show | 6 | HG02451.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-8250_-28-8248d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135876 | ||||||
chr6:110135906
|
T | C | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-8277A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135906 | ||||||
chr6:110135969
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-28-8340G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135969 | ||||||
chr6:110135975
|
C | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0102 | 2 | NA18971.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-28-8346G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135975 | ||||||
chr6:110135977
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28-8348C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110135977 | ||||||
chr6:110136106
|
G | A | 20 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28-8477C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136106 | ||||||
chr6:110136140
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-28-8511A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136140 | ||||||
chr6:110136154
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-8525C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136154 | ||||||
chr6:110136257
|
A | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-8628T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136257 | ||||||
chr6:110136335
|
T | G | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-8706A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136335 | ||||||
chr6:110136409
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28-8780G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136409 | ||||||
chr6:110136636
|
C | T | 2 | a0001c0001t0003g0124a0001c0001t0003g0125 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-28-9007G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136636 | ||||||
chr6:110136779
|
T | A | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-9150A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110136779 | ||||||
chr6:110137027
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-9398G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110137027 | ||||||
chr6:110137225
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-28-9596T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110137225 | ||||||
chr6:110137351
|
A | T | 1 | a0001c0001t0003g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28-9722T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110137351 | ||||||
chr6:110137640
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28-10011A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110137640 | ||||||
chr6:110137788
|
G | A | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-10159C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110137788 | ||||||
chr6:110138068
|
A | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG02965.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-28-10439T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138068 | ||||||
chr6:110138083
|
C | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28-10454G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138083 | ||||||
chr6:110138253
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-28-10624C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138253 | ||||||
chr6:110138293
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-10664C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138293 | ||||||
chr6:110138351
|
T | G | 1 | a0001c0001t0002g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-28-10722A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138351 | ||||||
chr6:110138494
|
T | C | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-28-10865A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138494 | ||||||
chr6:110138677
|
A | G | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11048T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138677 | ||||||
chr6:110138682
|
A | T | 1 | a0001c0001t0002g0249 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-28-11053T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138682 | ||||||
chr6:110138705
|
C | G | 1 | a0001c0002t0002g0201 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-11076G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138705 | ||||||
chr6:110138799
|
C | T | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11170G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138799 | ||||||
chr6:110138820
|
C | T | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28-11191G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138820 | ||||||
chr6:110138837
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-28-11208C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110138837 | ||||||
chr6:110139154
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-28-11525C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139154 | ||||||
chr6:110139159
|
T | C | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-28-11530A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139159 | ||||||
chr6:110139193
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-11564G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139193 | ||||||
chr6:110139194
|
G | A | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-11565C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139194 | ||||||
chr6:110139300
|
G | A | 1 | a0001c0001t0005g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-28-11671C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139300 | ||||||
chr6:110139363
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-28-11734G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139363 | ||||||
chr6:110139364
|
G | A | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-28-11735C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139364 | ||||||
chr6:110139406
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0148 | 2 | HG02071.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-28-11777C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139406 | ||||||
chr6:110139657
|
A | G | 4 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0160others(1): Show | 4 | NA18977.hp1 NA19063.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-12028T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139657 | ||||||
chr6:110139754
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-12125T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139754 | ||||||
chr6:110139859
|
A | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-12230T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139859 | ||||||
chr6:110139863
|
CTAA | C | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.-28-12237_-28-1223 others(7): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139863 | ||||||
chr6:110139912
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-12283T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139912 | ||||||
chr6:110139992
|
T | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-12363A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110139992 | ||||||
chr6:110140169
|
G | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-12540C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140169 | ||||||
chr6:110140172
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-12543A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140172 | ||||||
chr6:110140310
|
C | T | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-28-12681G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140310 | ||||||
chr6:110140331
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-28-12702T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140331 | ||||||
chr6:110140653
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-28-13024T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140653 | ||||||
chr6:110140747
|
C | G | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-13118G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110140747 | ||||||
chr6:110141013
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-13384T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141013 | ||||||
chr6:110141032
|
T | C | 1 | a0001c0001t0003g0102 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-28-13403A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141032 | ||||||
chr6:110141074
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-28-13445G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141074 | ||||||
chr6:110141118
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-28-13489C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141118 | ||||||
chr6:110141238
|
C | CTTCA | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02572.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-13613_-28-1361 others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141238 | ||||||
chr6:110141370
|
T | C | 24 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0154others(21): Show | 24 | HG00673.hp1 HG02027.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28-13741A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141370 | ||||||
chr6:110141440
|
T | G | 74 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0024others(71): Show | 74 | HG00280.hp1 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-28-13811A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141440 | ||||||
chr6:110141482
|
C | T | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-13853G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141482 | ||||||
chr6:110141574
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-28-13945G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141574 | ||||||
chr6:110141763
|
T | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-14134A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141763 | ||||||
chr6:110141772
|
CT | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-14144delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141772 | ||||||
chr6:110141850
|
C | T | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-28-14221G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141850 | ||||||
chr6:110141877
|
T | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-14248A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110141877 | ||||||
chr6:110142068
|
T | G | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-14439A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142068 | ||||||
chr6:110142081
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-14452G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142081 | ||||||
chr6:110142227
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-14598T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142227 | ||||||
chr6:110142308
|
A | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01074.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-14679T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142308 | ||||||
chr6:110142319
|
TTTCA | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-14694_-28-1469 others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142319 | ||||||
chr6:110142627
|
A | T | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28-14998T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142627 | ||||||
chr6:110142635
|
C | T | 20 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28-15006G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142635 | ||||||
chr6:110142709
|
CAG | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-15082_-28-1508 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142709 | ||||||
chr6:110142858
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0010g0138 | 3 | HG00280.hp2 HG00735.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-28-15229T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142858 | ||||||
chr6:110142952
|
T | TA | 178 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-28-15324dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAA | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-28-15325_-28-1532 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAA | 8 | a0001c0001t0001g0015a0001c0001t0004g0155a0001c0001t0006g0212others(5): Show | 8 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-15326_-28-1532 others(7): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(8): Show |
3 | a0001c0001t0004g0149a0001c0001t0005g0181a0001c0001t0005g0182 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-28-15338_-28-1532 others(19): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(9): Show |
6 | a0001c0001t0005g0183a0001c0001t0005g0184a0001c0001t0005g0185others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-15339_-28-1532 others(20): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(10): Show |
1 | a0001c0001t0004g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-28-15340_-28-1532 others(21): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(11): Show |
3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0179 | 3 | HG02647.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28-15341_-28-1532 others(22): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(13): Show |
6 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0160others(3): Show | 6 | HG02165.hp2 NA18939.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-15343_-28-1532 others(24): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(14): Show |
3 | a0001c0001t0004g0158a0001c0001t0004g0163a0001c0001t0004g0164 | 3 | HG00673.hp1 HG03491.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-28-15344_-28-1532 others(25): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(15): Show |
7 | a0001c0001t0004g0154a0001c0001t0004g0167a0001c0001t0004g0168others(4): Show | 7 | NA18950.hp2 NA18964.hp1 NA19007.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-15324_-28-1532 others(26): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(16): Show |
3 | a0001c0001t0004g0156a0001c0001t0004g0173a0001c0001t0004g0175 | 3 | HG02132.hp1 NA18955.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-28-15324_-28-1532 others(27): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(17): Show |
2 | a0001c0001t0004g0174a0001c0001t0004g0180 | 2 | HG02738.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-28-15324_-28-1532 others(28): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(19): Show |
1 | a0001c0001t0004g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28-15324_-28-1532 others(30): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
T | TAAAAAAA others(21): Show |
2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-28-15324_-28-1532 others(32): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110142952
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-15333_-28-1532 others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110142952 | ||||||
chr6:110143070
|
C | T | 21 | a0001c0001t0001g0035a0001c0001t0002g0189a0001c0001t0002g0190others(18): Show | 21 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-28-15441G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143070 | ||||||
chr6:110143160
|
A | T | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-15531T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143160 | ||||||
chr6:110143198
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-15569A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143198 | ||||||
chr6:110143347
|
T | TAA | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-15719_-28-1571 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143347 | ||||||
chr6:110143461
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-28-15832A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143461 | ||||||
chr6:110143480
|
A | T | 1 | a0001c0001t0003g0019 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-28-15851T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143480 | ||||||
chr6:110143624
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-28-15995A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143624 | ||||||
chr6:110143649
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28-16020C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143649 | ||||||
chr6:110143829
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-28-16200T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143829 | ||||||
chr6:110143839
|
A | AT | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0241 | 3 | NA18959.hp1 NA18964.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.-28-16211dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143839 | ||||||
chr6:110143905
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28-16276A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143905 | ||||||
chr6:110143925
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-28-16296C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110143925 | ||||||
chr6:110144053
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-28-16424C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144053 | ||||||
chr6:110144164
|
G | A | 1 | a0001c0001t0004g0165 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-29+16471C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144164 | ||||||
chr6:110144180
|
C | T | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-29+16455G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144180 | ||||||
chr6:110144448
|
G | C | 3 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122 | 3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-29+16187C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144448 | ||||||
chr6:110144468
|
T | C | 1 | a0001c0002t0002g0206 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29+16167A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144468 | ||||||
chr6:110144558
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-29+16077T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144558 | ||||||
chr6:110144558
|
A | T | 3 | a0001c0001t0004g0157a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02451.hp1 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+16077T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144558 | ||||||
chr6:110144559
|
T | A | 3 | a0001c0001t0004g0157a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02451.hp1 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+16076A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144559 | ||||||
chr6:110144560
|
A | T | 3 | a0001c0001t0004g0157a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02451.hp1 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+16075T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144560 | ||||||
chr6:110144599
|
C | T | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+16036G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144599 | ||||||
chr6:110144604
|
G | C | 2 | a0001c0001t0004g0178a0001c0001t0004g0179 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-29+16031C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144604 | ||||||
chr6:110144606
|
G | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0179 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-29+16029C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144606 | ||||||
chr6:110144683
|
G | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+15952C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144683 | ||||||
chr6:110144812
|
G | A | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+15823C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144812 | ||||||
chr6:110144818
|
C | A | 19 | a0001c0001t0001g0137a0001c0002t0002g0191a0001c0002t0002g0192others(16): Show | 19 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29+15817G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144818 | ||||||
chr6:110144895
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+15740G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144895 | ||||||
chr6:110144935
|
G | A | 23 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(20): Show | 23 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.-29+15700C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144935 | ||||||
chr6:110144943
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-29+15692G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110144943 | ||||||
chr6:110145071
|
C | T | 47 | a0001c0001t0002g0218a0001c0001t0004g0149a0001c0001t0004g0150others(44): Show | 47 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(44): Show |
intron_variant | MODIFIER | c.-29+15564G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145071 | ||||||
chr6:110145183
|
C | T | 4 | a0001c0001t0001g0144a0001c0002t0002g0207a0001c0002t0002g0208others(1): Show | 4 | HG02451.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+15452G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145183 | ||||||
chr6:110145367
|
A | G | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-29+15268T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145367 | ||||||
chr6:110145901
|
A | G | 1 | a0001c0001t0004g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-29+14734T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145901 | ||||||
chr6:110145945
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-29+14690T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145945 | ||||||
chr6:110145973
|
G | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+14662C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110145973 | ||||||
chr6:110146266
|
T | A | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-29+14369A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146266 | ||||||
chr6:110146358
|
A | AAATAATT others(314): Show |
1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29+14276_-29+1427 others(325): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146358 | ||||||
chr6:110146628
|
C | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+14007G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146628 | ||||||
chr6:110146744
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+13891G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146744 | ||||||
chr6:110146843
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-29+13792T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146843 | ||||||
chr6:110146854
|
A | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+13781T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146854 | ||||||
chr6:110146947
|
A | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29+13688T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110146947 | ||||||
chr6:110147114
|
G | A | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+13521C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147114 | ||||||
chr6:110147122
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-29+13513A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147122 | ||||||
chr6:110147207
|
G | A | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+13428C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147207 | ||||||
chr6:110147294
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29+13341G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147294 | ||||||
chr6:110147345
|
C | CA | 41 | a0001c0001t0001g0118a0001c0001t0002g0219a0001c0001t0002g0221others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-29+13289dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147345 | ||||||
chr6:110147345
|
CA | C | 41 | a0001c0001t0003g0039a0001c0001t0004g0149a0001c0001t0004g0150others(38): Show | 41 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(38): Show |
intron_variant | MODIFIER | c.-29+13289delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147345 | ||||||
chr6:110147346
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-29+13289T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147346 | ||||||
chr6:110147349
|
A | T | 1 | a0001c0001t0003g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-29+13286T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147349 | ||||||
chr6:110147363
|
A | T | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-29+13272T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147363 | ||||||
chr6:110147511
|
CAG | C | 3 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0003g0131 | 3 | HG02145.hp1 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+13122_-29+1312 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147511 | ||||||
chr6:110147613
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-29+13022T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147613 | ||||||
chr6:110147790
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-29+12845T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147790 | ||||||
chr6:110147924
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-29+12711A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110147924 | ||||||
chr6:110148098
|
A | G | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+12537T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148098 | ||||||
chr6:110148142
|
T | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+12493A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148142 | ||||||
chr6:110148145
|
C | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+12490G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148145 | ||||||
chr6:110148182
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29+12453A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148182 | ||||||
chr6:110148252
|
TAACC | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+12379_-29+1238 others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148252 | ||||||
chr6:110148437
|
A | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-29+12198T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148437 | ||||||
chr6:110148480
|
A | T | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29+12155T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148480 | ||||||
chr6:110148507
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02572.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+12128A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148507 | ||||||
chr6:110148851
|
T | C | 1 | a0001c0001t0003g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-29+11784A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110148851 | ||||||
chr6:110149119
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-29+11516C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149119 | ||||||
chr6:110149178
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29+11457C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149178 | ||||||
chr6:110149255
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+11380C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149255 | ||||||
chr6:110149311
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-29+11324C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149311 | ||||||
chr6:110149313
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29+11322G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149313 | ||||||
chr6:110149484
|
T | TA | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(6): Show | 9 | HG01106.hp1 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+11150dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149484 | ||||||
chr6:110149484
|
TA | T | 27 | a0001c0001t0002g0190a0001c0001t0002g0209a0001c0001t0002g0211others(24): Show | 27 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+11150delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149484 | ||||||
chr6:110149484
|
TAA | T | 50 | a0001c0001t0002g0210a0001c0001t0004g0149a0001c0001t0004g0150others(47): Show | 50 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-29+11149_-29+1115 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149484 | ||||||
chr6:110149992
|
G | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+10643C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110149992 | ||||||
chr6:110150092
|
T | C | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+10543A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150092 | ||||||
chr6:110150161
|
T | C | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+10474A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150161 | ||||||
chr6:110150219
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+10416T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150219 | ||||||
chr6:110150251
|
T | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+10384A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150251 | ||||||
chr6:110150345
|
T | C | 19 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0004g0155others(16): Show | 19 | HG00673.hp1 HG02027.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29+10290A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150345 | ||||||
chr6:110150452
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | HG01517.hp2 HG03490.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+10183G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150452 | ||||||
chr6:110150670
|
A | AT | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-29+9964dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150670 | ||||||
chr6:110150800
|
C | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29+9835G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150800 | ||||||
chr6:110150807
|
G | A | 6 | a0001c0001t0003g0021a0001c0001t0003g0025a0001c0001t0003g0052others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+9828C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150807 | ||||||
chr6:110150865
|
G | A | 29 | a0001c0001t0002g0190a0001c0001t0004g0149a0001c0001t0004g0150others(26): Show | 29 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29+9770C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110150865 | ||||||
chr6:110151077
|
A | G | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+9558T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151077 | ||||||
chr6:110151185
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29+9450C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151185 | ||||||
chr6:110151316
|
C | A | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+9319G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151316 | ||||||
chr6:110151488
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+9147G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151488 | ||||||
chr6:110151627
|
CTTTATA | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02572.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+9002_-29+9007d others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151627 | ||||||
chr6:110151730
|
T | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+8905A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151730 | ||||||
chr6:110151777
|
A | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+8858T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151777 | ||||||
chr6:110151848
|
T | G | 1 | a0001c0001t0004g0165 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-29+8787A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151848 | ||||||
chr6:110151979
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29+8656C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110151979 | ||||||
chr6:110152039
|
T | C | 1 | a0001c0001t0006g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-29+8596A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152039 | ||||||
chr6:110152287
|
G | A | 1 | a0001c0001t0003g0102 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-29+8348C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152287 | ||||||
chr6:110152337
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29+8298G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152337 | ||||||
chr6:110152419
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-29+8216T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152419 | ||||||
chr6:110152594
|
T | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | NA18951.hp1 NA18978.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-29+8041A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152594 | ||||||
chr6:110152673
|
A | G | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.-29+7962T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110152673 | ||||||
chr6:110153067
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-29+7568A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153067 | ||||||
chr6:110153189
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+7446G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153189 | ||||||
chr6:110153288
|
T | C | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+7347A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153288 | ||||||
chr6:110153387
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-29+7248C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153387 | ||||||
chr6:110153395
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0105 | 2 | NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-29+7240A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153395 | ||||||
chr6:110153560
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+7075A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153560 | ||||||
chr6:110153684
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29+6951C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153684 | ||||||
chr6:110153701
|
C | T | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+6934G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153701 | ||||||
chr6:110153792
|
G | GA | 40 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(37): Show | 40 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-29+6842dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153792 | ||||||
chr6:110153849
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-29+6786T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110153849 | ||||||
chr6:110154239
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+6396G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154239 | ||||||
chr6:110154583
|
A | T | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+6052T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154583 | ||||||
chr6:110154589
|
C | T | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-29+6046G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154589 | ||||||
chr6:110154712
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29+5923A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154712 | ||||||
chr6:110154737
|
C | T | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+5898G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154737 | ||||||
chr6:110154944
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-29+5691T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154944 | ||||||
chr6:110154966
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-29+5669T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110154966 | ||||||
chr6:110155012
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-29+5623A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155012 | ||||||
chr6:110155082
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-29+5553G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155082 | ||||||
chr6:110155234
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-29+5401C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155234 | ||||||
chr6:110155283
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG01074.hp2 HG02572.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+5352C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155283 | ||||||
chr6:110155332
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+5303G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155332 | ||||||
chr6:110155484
|
C | T | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-29+5151G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155484 | ||||||
chr6:110155509
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+5126T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155509 | ||||||
chr6:110155522
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-29+5113A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155522 | ||||||
chr6:110155523
|
TCTAAAGT others(3034): Show |
T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+2071_-29+5111d others(2): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155523 | ||||||
chr6:110155536
|
C | CT | 72 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(69): Show | 72 | HG00639.hp2 HG00673.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+5098dupA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
C | CTT | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0107others(3): Show | 6 | HG01106.hp1 HG01175.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+5097_-29+5098d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
CT | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 29 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29+5098delA | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
CTT | C | 35 | a0001c0001t0001g0010a0001c0001t0002g0219a0001c0001t0002g0222others(32): Show | 35 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-29+5097_-29+5098d others(4): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
CTTT | C | 12 | a0001c0001t0002g0211a0001c0001t0002g0218a0001c0001t0002g0234others(9): Show | 12 | HG00639.hp1 HG01891.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+5096_-29+5098d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-29+5089_-29+5098d others(12): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155536
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(5): Show | 8 | HG01081.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+5087_-29+5098d others(14): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155536 | ||||||
chr6:110155619
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-29+5016A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155619 | ||||||
chr6:110155698
|
C | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+4937G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155698 | ||||||
chr6:110155823
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-29+4812T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155823 | ||||||
chr6:110155936
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29+4699G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155936 | ||||||
chr6:110155964
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29+4671A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110155964 | ||||||
chr6:110156074
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29+4561A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156074 | ||||||
chr6:110156087
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-29+4548A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156087 | ||||||
chr6:110156101
|
T | C | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29+4534A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156101 | ||||||
chr6:110156197
|
G | A | 8 | a0001c0001t0002g0218a0001c0001t0003g0106a0001c0001t0006g0212others(5): Show | 8 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+4438C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156197 | ||||||
chr6:110156238
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-29+4397A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156238 | ||||||
chr6:110156343
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 221 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-29+4292C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156343 | ||||||
chr6:110156364
|
G | A | 20 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-29+4271C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156364 | ||||||
chr6:110156438
|
T | A | 1 | a0001c0001t0003g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29+4197A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156438 | ||||||
chr6:110156495
|
G | T | 1 | a0001c0001t0002g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-29+4140C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156495 | ||||||
chr6:110156496
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-29+4139A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156496 | ||||||
chr6:110156565
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-29+4070G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156565 | ||||||
chr6:110156720
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG01074.hp2 HG03831.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-29+3915A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156720 | ||||||
chr6:110156828
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29+3807A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156828 | ||||||
chr6:110156845
|
G | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+3790C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156845 | ||||||
chr6:110156861
|
T | A | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+3774A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156861 | ||||||
chr6:110156935
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-29+3700G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110156935 | ||||||
chr6:110157031
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-29+3604T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157031 | ||||||
chr6:110157131
|
T | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+3504A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157131 | ||||||
chr6:110157273
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-29+3362G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157273 | ||||||
chr6:110157290
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-29+3345A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157290 | ||||||
chr6:110157394
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+3241A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157394 | ||||||
chr6:110157463
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-29+3172C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157463 | ||||||
chr6:110157532
|
T | C | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+3103A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157532 | ||||||
chr6:110157604
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0002c0007t0001g0047 | 3 | HG01433.hp1 HG01516.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-29+3031G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157604 | ||||||
chr6:110157605
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-29+3030C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157605 | ||||||
chr6:110157629
|
G | T | 1 | a0001c0001t0003g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-29+3006C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157629 | ||||||
chr6:110157639
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-29+2996G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157639 | ||||||
chr6:110157714
|
T | C | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+2921A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157714 | ||||||
chr6:110157724
|
C | G | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+2911G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157724 | ||||||
chr6:110157725
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-29+2910C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157725 | ||||||
chr6:110157745
|
A | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+2890T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157745 | ||||||
chr6:110157767
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-29+2868C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157767 | ||||||
chr6:110157767
|
G | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+2868C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157767 | ||||||
chr6:110157910
|
T | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(7): Show | 10 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+2725A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157910 | ||||||
chr6:110157983
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-29+2652A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157983 | ||||||
chr6:110157985
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-29+2650T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157985 | ||||||
chr6:110157997
|
G | A | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-29+2638C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110157997 | ||||||
chr6:110158161
|
A | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | NA18955.hp1 NA18971.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+2474T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158161 | ||||||
chr6:110158165
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-29+2470T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158165 | ||||||
chr6:110158265
|
T | A | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+2370A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158265 | ||||||
chr6:110158323
|
G | C | 1 | a0001c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29+2312C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158323 | ||||||
chr6:110158406
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+2229G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158406 | ||||||
chr6:110158407
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-29+2228G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158407 | ||||||
chr6:110158797
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-29+1838A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158797 | ||||||
chr6:110158927
|
G | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+1708C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158927 | ||||||
chr6:110158948
|
AATT | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02572.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+1684_-29+1686d others(5): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110158948 | ||||||
chr6:110159015
|
T | C | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+1620A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159015 | ||||||
chr6:110159098
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-29+1537C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159098 | ||||||
chr6:110159476
|
CTTTACT | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+1153_-29+1158d others(8): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159476 | ||||||
chr6:110159497
|
C | T | 18 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(15): Show | 18 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+1138G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159497 | ||||||
chr6:110159549
|
T | C | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+1086A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159549 | ||||||
chr6:110159650
|
A | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+985T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110159650 | ||||||
chr6:110160415
|
T | C | 1 | a0001c0001t0006g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-29+220A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110160415 | ||||||
chr6:110160550
|
C | T | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.-29+85G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110160550 | ||||||
chr6:110160577
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-29+58A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 3/10 | chr6 | 110160577 | ||||||
chr6:110161057
|
A | T | 1 | a0001c0001t0003g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-126-325T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161057 | ||||||
chr6:110161176
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-126-444A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161176 | ||||||
chr6:110161359
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-126-627A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161359 | ||||||
chr6:110161506
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-126-774G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161506 | ||||||
chr6:110161561
|
T | G | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-126-829A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161561 | ||||||
chr6:110161630
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-898T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161630 | ||||||
chr6:110161691
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-126-959C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110161691 | ||||||
chr6:110162014
|
G | A | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-126-1282C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162014 | ||||||
chr6:110162018
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-1286C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162018 | ||||||
chr6:110162058
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-126-1326A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162058 | ||||||
chr6:110162376
|
C | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-1644G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162376 | ||||||
chr6:110162436
|
A | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-126-1704T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162436 | ||||||
chr6:110162442
|
C | CA | 19 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0134others(16): Show | 19 | HG00741.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-126-1711dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162442 | ||||||
chr6:110162751
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-126-2019C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162751 | ||||||
chr6:110162884
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-126-2152C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162884 | ||||||
chr6:110162935
|
G | A | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-2203C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110162935 | ||||||
chr6:110163125
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-126-2393T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163125 | ||||||
chr6:110163360
|
A | G | 1 | a0001c0002t0002g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-126-2628T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163360 | ||||||
chr6:110163374
|
C | T | 41 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-126-2642G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163374 | ||||||
chr6:110163465
|
G | A | 1 | a0001c0001t0004g0155 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-126-2733C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163465 | ||||||
chr6:110163662
|
C | A | 1 | a0001c0006t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-126-2930G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163662 | ||||||
chr6:110163756
|
C | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-3024G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163756 | ||||||
chr6:110163829
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126-3097G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110163829 | ||||||
chr6:110164038
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-126-3306G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164038 | ||||||
chr6:110164339
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG02572.hp1 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-3607A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164339 | ||||||
chr6:110164423
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG01081.hp2 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-3691G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164423 | ||||||
chr6:110164546
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-126-3814T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164546 | ||||||
chr6:110164666
|
C | G | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-126-3934G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164666 | ||||||
chr6:110164740
|
G | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 122 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.-126-4008C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164740 | ||||||
chr6:110164814
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-126-4082A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164814 | ||||||
chr6:110164905
|
C | T | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-4173G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164905 | ||||||
chr6:110164918
|
T | A | 1 | a0001c0001t0005g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-126-4186A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164918 | ||||||
chr6:110164922
|
C | A | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-126-4190G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164922 | ||||||
chr6:110164936
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-126-4204C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164936 | ||||||
chr6:110164975
|
T | A | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-126-4243A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110164975 | ||||||
chr6:110165014
|
A | G | 3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0259 | 3 | HG01891.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-126-4282T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165014 | ||||||
chr6:110165051
|
A | C | 1 | a0001c0001t0002g0244 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-126-4319T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165051 | ||||||
chr6:110165209
|
G | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 11 | HG00735.hp2 HG01168.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-126-4477C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165209 | ||||||
chr6:110165258
|
T | C | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-126-4526A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165258 | ||||||
chr6:110165401
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-126-4669C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165401 | ||||||
chr6:110165807
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-126-5075G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165807 | ||||||
chr6:110165813
|
A | C | 1 | a0001c0001t0003g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126-5081T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165813 | ||||||
chr6:110165818
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-126-5086A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110165818 | ||||||
chr6:110166165
|
T | C | 14 | a0001c0001t0002g0244a0001c0001t0002g0245a0001c0001t0002g0246others(11): Show | 14 | HG00408.hp2 HG00639.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-126-5433A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166165 | ||||||
chr6:110166358
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-126-5626G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166358 | ||||||
chr6:110166412
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-5680G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166412 | ||||||
chr6:110166439
|
T | C | 1 | a0001c0002t0002g0198 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-126-5707A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166439 | ||||||
chr6:110166611
|
C | T | 2 | a0001c0001t0003g0039a0001c0001t0003g0040 | 2 | HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-126-5879G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166611 | ||||||
chr6:110166669
|
T | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-5937A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166669 | ||||||
chr6:110166727
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-126-5995A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166727 | ||||||
chr6:110166746
|
A | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-126-6014T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166746 | ||||||
chr6:110166839
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-126-6107A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166839 | ||||||
chr6:110166864
|
A | T | 1 | a0001c0001t0003g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-126-6132T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166864 | ||||||
chr6:110166903
|
T | A | 41 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(38): Show | 41 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-126-6171A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110166903 | ||||||
chr6:110167158
|
G | GA | 111 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(108): Show | 111 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-126-6427dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167158 | ||||||
chr6:110167179
|
C | T | 1 | a0001c0001t0004g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-126-6447G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167179 | ||||||
chr6:110167379
|
T | C | 1 | a0001c0002t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-126-6647A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167379 | ||||||
chr6:110167420
|
T | A | 1 | a0001c0001t0003g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-126-6688A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167420 | ||||||
chr6:110167634
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0003g0120a0001c0001t0003g0121others(1): Show | 4 | HG03490.hp1 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126-6902A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167634 | ||||||
chr6:110167700
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-126-6968G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167700 | ||||||
chr6:110167959
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-126-7227C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110167959 | ||||||
chr6:110168173
|
G | A | 1 | a0001c0001t0003g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-126-7441C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110168173 | ||||||
chr6:110168290
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG01074.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126-7558C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110168290 | ||||||
chr6:110168354
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-126-7622A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110168354 | ||||||
chr6:110169086
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-126-8354A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169086 | ||||||
chr6:110169112
|
C | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG01358.hp2 HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-126-8380G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169112 | ||||||
chr6:110169367
|
G | A | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-126-8635C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169367 | ||||||
chr6:110169546
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-126-8814G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169546 | ||||||
chr6:110169559
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126-8827G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169559 | ||||||
chr6:110169662
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-126-8930T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169662 | ||||||
chr6:110169734
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+8864A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169734 | ||||||
chr6:110169763
|
T | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+8835A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110169763 | ||||||
chr6:110170149
|
T | A | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+8449A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170149 | ||||||
chr6:110170213
|
G | A | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+8385C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170213 | ||||||
chr6:110170247
|
G | C | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+8351C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170247 | ||||||
chr6:110170261
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-127+8337G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170261 | ||||||
chr6:110170277
|
T | C | 2 | a0001c0001t0003g0124a0001c0001t0003g0125 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-127+8321A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170277 | ||||||
chr6:110170279
|
G | T | 8 | a0001c0002t0002g0191a0001c0002t0002g0192a0001c0002t0002g0193others(5): Show | 8 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-127+8319C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170279 | ||||||
chr6:110170380
|
A | G | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+8218T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170380 | ||||||
chr6:110170551
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+8047G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170551 | ||||||
chr6:110170670
|
TA | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+7927delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170670 | ||||||
chr6:110170692
|
A | G | 1 | a0001c0001t0003g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-127+7906T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170692 | ||||||
chr6:110170860
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-127+7738A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110170860 | ||||||
chr6:110171361
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-127+7237A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171361 | ||||||
chr6:110171485
|
A | G | 113 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.-127+7113T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171485 | ||||||
chr6:110171487
|
C | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+7111G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171487 | ||||||
chr6:110171488
|
G | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+7110C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171488 | ||||||
chr6:110171767
|
T | C | 32 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(29): Show | 32 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.-127+6831A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171767 | ||||||
chr6:110171994
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-127+6604G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110171994 | ||||||
chr6:110172126
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-127+6472C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172126 | ||||||
chr6:110172220
|
A | G | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+6378T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172220 | ||||||
chr6:110172228
|
G | A | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+6370C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172228 | ||||||
chr6:110172393
|
C | T | 1 | a0001c0001t0003g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-127+6205G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172393 | ||||||
chr6:110172699
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-127+5899A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172699 | ||||||
chr6:110172750
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-127+5848T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172750 | ||||||
chr6:110172758
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-127+5840T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172758 | ||||||
chr6:110172848
|
A | G | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+5750T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172848 | ||||||
chr6:110172974
|
C | T | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+5624G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110172974 | ||||||
chr6:110173006
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-127+5592A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173006 | ||||||
chr6:110173068
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-127+5530T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173068 | ||||||
chr6:110173214
|
A | G | 20 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0002t0002g0191others(17): Show | 20 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-127+5384T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173214 | ||||||
chr6:110173238
|
T | A | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-127+5360A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173238 | ||||||
chr6:110173428
|
T | C | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-127+5170A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173428 | ||||||
chr6:110173598
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+5000C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173598 | ||||||
chr6:110173644
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-127+4954G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173644 | ||||||
chr6:110173732
|
G | T | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+4866C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173732 | ||||||
chr6:110173739
|
C | A | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+4859G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173739 | ||||||
chr6:110173740
|
T | C | 24 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0209others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-127+4858A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173740 | ||||||
chr6:110173869
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+4729A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110173869 | ||||||
chr6:110174111
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-127+4487G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174111 | ||||||
chr6:110174201
|
A | G | 3 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0003g0131 | 3 | HG02145.hp1 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-127+4397T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174201 | ||||||
chr6:110174226
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-127+4372G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174226 | ||||||
chr6:110174227
|
CCT | C | 4 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+4369_-127+437 others(6): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174227 | ||||||
chr6:110174401
|
T | G | 1 | a0001c0001t0004g0175 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-127+4197A>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174401 | ||||||
chr6:110174416
|
A | T | 1 | a0001c0001t0002g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-127+4182T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174416 | ||||||
chr6:110174661
|
A | G | 1 | a0001c0001t0003g0023 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-127+3937T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174661 | ||||||
chr6:110174862
|
C | T | 7 | a0001c0001t0002g0218a0001c0001t0006g0212a0001c0001t0006g0213others(4): Show | 7 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-127+3736G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174862 | ||||||
chr6:110174899
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-127+3699A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110174899 | ||||||
chr6:110175085
|
T | A | 1 | a0001c0001t0002g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-127+3513A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175085 | ||||||
chr6:110175200
|
A | G | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.-127+3398T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175200 | ||||||
chr6:110175233
|
G | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+3365C>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175233 | ||||||
chr6:110175291
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-127+3307G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175291 | ||||||
chr6:110175494
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+3104G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175494 | ||||||
chr6:110175509
|
T | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+3089A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175509 | ||||||
chr6:110175596
|
C | T | 2 | a0001c0001t0004g0152a0001c0001t0004g0153 | 2 | NA19063.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-127+3002G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175596 | ||||||
chr6:110175701
|
T | C | 42 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 42 | HG00408.hp2 HG00639.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-127+2897A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175701 | ||||||
chr6:110175724
|
T | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-127+2874A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175724 | ||||||
chr6:110175838
|
G | A | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-127+2760C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110175838 | ||||||
chr6:110176030
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-127+2568A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176030 | ||||||
chr6:110176149
|
ATAAACT | A | 9 | a0001c0001t0004g0167a0001c0001t0004g0168a0001c0001t0004g0169others(6): Show | 9 | NA18950.hp2 NA18955.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127+2443_-127+244 others(10): Show |
WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176149 | ||||||
chr6:110176348
|
A | T | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-127+2250T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176348 | ||||||
chr6:110176582
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-127+2016T>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176582 | ||||||
chr6:110176883
|
A | G | 1 | a0001c0001t0004g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-127+1715T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176883 | ||||||
chr6:110176901
|
A | G | 6 | a0001c0001t0006g0212a0001c0001t0006g0213a0001c0001t0006g0214others(3): Show | 6 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+1697T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176901 | ||||||
chr6:110176984
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-127+1614T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176984 | ||||||
chr6:110176986
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-127+1612C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110176986 | ||||||
chr6:110177006
|
C | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-127+1592G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177006 | ||||||
chr6:110177037
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-127+1561G>A | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177037 | ||||||
chr6:110177323
|
T | C | 5 | a0001c0001t0003g0129a0001c0001t0003g0130a0001c0001t0003g0131others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+1275A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177323 | ||||||
chr6:110177349
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-127+1249T>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177349 | ||||||
chr6:110177931
|
G | A | 28 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(25): Show | 28 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.-127+667C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177931 | ||||||
chr6:110177945
|
C | CA | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+652dupT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177945 | ||||||
chr6:110177945
|
CA | C | 26 | a0001c0001t0001g0020a0001c0001t0002g0189a0001c0001t0002g0190others(23): Show | 26 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-127+652delT | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177945 | ||||||
chr6:110177988
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-127+610A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110177988 | ||||||
chr6:110178078
|
A | C | 1 | a0001c0001t0003g0019 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-127+520T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110178078 | ||||||
chr6:110178196
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA18968.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-127+402A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110178196 | ||||||
chr6:110178477
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02451.hp1 HG03195.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-127+121C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110178477 | ||||||
chr6:110178527
|
T | A | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+71A>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 2/10 | chr6 | 110178527 | ||||||
chr6:110178795
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-271-53A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110178795 | ||||||
chr6:110178962
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-271-220C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110178962 | ||||||
chr6:110179031
|
G | C | 8 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-271-289C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179031 | ||||||
chr6:110179039
|
G | A | 1 | a0001c0001t0003g0140 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-271-297C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179039 | ||||||
chr6:110179095
|
G | A | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0004g0180 | 3 | HG02723.hp1 HG02738.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-272+344C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179095 | ||||||
chr6:110179152
|
C | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.-272+287G>C | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179152 | ||||||
chr6:110179305
|
G | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(1): Show | 4 | HG02083.hp2 HG02523.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-272+134C>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179305 | ||||||
chr6:110179318
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-272+121G>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179318 | ||||||
chr6:110179342
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-272+97C>T | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179342 | ||||||
chr6:110179372
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-272+67A>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179372 | ||||||
chr6:110179392
|
A | C | 40 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(37): Show | 40 | HG00673.hp1 HG01516.hp1 HG01517.hp1 others(37): Show |
intron_variant | MODIFIER | c.-272+47T>G | WASF1 | ENSG00000112290.13 | transcript | ENST00000392589.6 | protein_coding | 1/10 | chr6 | 110179392 |