geneid | 6009 |
---|---|
ensemblid | ENSG00000106615.10 |
hgncid | 10011 |
symbol | RHEB |
name | Ras homolog, mTORC1 binding |
refseq_nuc | NM_005614.4 |
refseq_prot | NP_005605.1 |
ensembl_nuc | ENST00000262187.10 |
ensembl_prot | ENSP00000262187.5 |
mane_status | MANE Select |
chr | chr7 |
start | 151466012 |
end | 151519895 |
strand | - |
ver | v1.2 |
region | chr7:151466012-151519895 |
region5000 | chr7:151461012-151524895 |
regionname0 | RHEB_chr7_151466012_151519895 |
regionname5000 | RHEB_chr7_151461012_151524895 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 184 | 364 | 86 | 70 | 158 | 14 | 34 | 122 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 555 | 360 | 84 | 70 | 156 | 14 | 34 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
c0002 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
c0003 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
c0004 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
c0005 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1492 | 303 | 61 | 60 | 137 | 12 | 31 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0002 | 0/0 | 1501 | 40 | 14 | 10 | 15 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0003 | 0/0 | 1488 | 7 | 7 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0004 | 0/0 | 1492 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0005 | 0/0 | 1492 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0006 | 0/0 | 1492 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0007 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0008 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0009 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0010 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0011 | 0/0 | 1492 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0012 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
t0013 | 0/0 | 1492 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0003 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0004 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 555 | 360 | 84 | 70 | 156 | 14 | 34 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0002 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0003 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0004 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0005 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2046 | 299 | 59 | 60 | 135 | 12 | 31 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0002 | 0/0 | 2055 | 40 | 14 | 10 | 15 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0003 | 0/0 | 2042 | 7 | 7 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0004 | 0/0 | 2046 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0005 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0006 | 0/0 | 2046 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0007 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0008 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0009 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0010 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0011 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0012 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0001t0013 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0002t0001 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0003t0001 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0004t0001 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
a0001c0005t0001 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | copy fasta | chr7 | 151461012 | 151524895 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0012g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0001t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
a0001c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00099 | hp2 | a0001 | c0001 | t0007 | g0036 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00323 | hp2 | a0001 | c0001 | t0010 | g0141 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00408 | hp2 | a0001 | c0001 | t0012 | g0233 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02602 | hp2 | a0001 | c0001 | t0011 | g0188 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0301 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04228 | hp1 | a0001 | c0001 | t0009 | g0059 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19007 | hp2 | a0001 | c0004 | t0001 | g0154 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0300 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ASW | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ASW | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | TSI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | USA | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0183 | REF | REF | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0101 | REF | REF | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151467134
|
T | C | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.540A>G | p.Ser180Ser | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 924/2046 | 540/555 | 180/184 | chr7 | 151467134 | ||
chr7:151471432
|
A | G | 1 | a0001c0002 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.342T>C | p.Ile114Ile | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/8 | 726/2046 | 342/555 | 114/184 | chr7 | 151471432 | ||
chr7:151490992
|
T | C | 1 | a0001c0004 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.75A>G | p.Gln25Gln | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/8 | 459/2046 | 75/555 | 25/184 | chr7 | 151490992 | ||
chr7:151519479
|
G | A | 1 | a0001c0005 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.33C>T | p.Ile11Ile | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 417/2046 | 33/555 | 11/184 | chr7 | 151519479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151466162
|
CCAAA | C | 1 | a0001c0001t0003 | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*953_*956delTTTG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 953 | chr7 | 151466162 | |||||
chr7:151466192
|
C | A | 1 | a0001c0001t0006 | 2 | NA18955.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 927 | chr7 | 151466192 | |||||
chr7:151466308
|
C | T | 1 | a0001c0001t0005 | 2 | HG02630.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*811G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 811 | chr7 | 151466308 | |||||
chr7:151466337
|
C | G | 1 | a0001c0001t0010 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 782 | chr7 | 151466337 | |||||
chr7:151466562
|
C | CTGCGCAG others(2): Show |
1 | a0001c0001t0002 | 40 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*557insTCCTGC others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 556 | chr7 | 151466562 | |||||
chr7:151466715
|
T | G | 1 | a0001c0001t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 404 | chr7 | 151466715 | |||||
chr7:151466721
|
C | T | 1 | a0001c0001t0009 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 398 | chr7 | 151466721 | |||||
chr7:151466861
|
C | T | 1 | a0001c0001t0013 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 258 | chr7 | 151466861 | |||||
chr7:151466905
|
T | C | 1 | a0001c0001t0012 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 214 | chr7 | 151466905 | |||||
chr7:151467028
|
A | C | 1 | a0001c0001t0003 | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*91T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 91 | chr7 | 151467028 | |||||
chr7:151519512
|
C | A | 1 | a0001c0001t0013 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 1 | chr7 | 151519512 | |||||
chr7:151519707
|
C | G | 1 | a0001c0001t0004 | 3 | NA18981.hp1 NA19005.hp2 NA19078.hp1 |
5_prime_UTR_variant | MODIFIER | c.-196G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 196 | chr7 | 151519707 | |||||
chr7:151519850
|
C | T | 1 | a0001c0001t0008 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-339G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 339 | chr7 | 151519850 | |||||
chr7:151519858
|
A | G | 1 | a0001c0001t0007 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-347T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 347 | chr7 | 151519858 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151467262
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(105): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.463-51C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467262 | ||||||
chr7:151467275
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.463-64C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467275 | ||||||
chr7:151467386
|
C | T | 10 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0048others(7): Show | 10 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-175G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467386 | ||||||
chr7:151467536
|
T | TG | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(297): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.463-326dupC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467536 | ||||||
chr7:151467758
|
T | C | 62 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(59): Show | 67 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.463-547A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467758 | ||||||
chr7:151467759
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0184 | 2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.463-548G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467759 | ||||||
chr7:151468010
|
C | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0148 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.463-799G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468010 | ||||||
chr7:151468285
|
C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(109): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.463-1074G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468285 | ||||||
chr7:151468391
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.463-1180C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468391 | ||||||
chr7:151468406
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0258others(3): Show | 8 | HG01243.hp1 HG01943.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.463-1195C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468406 | ||||||
chr7:151468407
|
C | T | 16 | a0001c0001t0001g0030a0001c0001t0001g0083a0001c0001t0001g0180others(13): Show | 17 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.463-1196G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468407 | ||||||
chr7:151468507
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.463-1296G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468507 | ||||||
chr7:151468594
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.463-1383C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468594 | ||||||
chr7:151469041
|
T | A | 1 | a0001c0001t0002g0068 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.462+1530A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469041 | ||||||
chr7:151469166
|
A | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.462+1405T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469166 | ||||||
chr7:151469171
|
GTTT | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0258others(2): Show | 7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+1397_462+1399d others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469171 | ||||||
chr7:151469377
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0182others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+1194T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469377 | ||||||
chr7:151469457
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0217others(7): Show | 16 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.462+1114C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469457 | ||||||
chr7:151469517
|
TC | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.462+1053delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469517 | ||||||
chr7:151469566
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.462+1005A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469566 | ||||||
chr7:151469755
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.462+816C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469755 | ||||||
chr7:151469845
|
G | T | 1 | a0001c0001t0013g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.462+726C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469845 | ||||||
chr7:151469889
|
G | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0076 | 3 | HG02040.hp1 HG02132.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.462+682C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469889 | ||||||
chr7:151470345
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.462+226A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151470345 | ||||||
chr7:151470360
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.462+211G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151470360 | ||||||
chr7:151470741
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.381-89C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470741 | ||||||
chr7:151470754
|
C | G | 1 | a0001c0001t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.381-102G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470754 | ||||||
chr7:151470843
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.381-191T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470843 | ||||||
chr7:151470917
|
T | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0096 | 3 | HG01167.hp2 HG01358.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.381-265A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470917 | ||||||
chr7:151470965
|
A | G | 1 | a0001c0001t0005g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.381-313T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470965 | ||||||
chr7:151471065
|
G | A | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+329C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471065 | ||||||
chr7:151471200
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.380+194A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471200 | ||||||
chr7:151471307
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380+87T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471307 | ||||||
chr7:151471329
|
CAAT | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.380+62_380+64delAT others(1): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471329 | ||||||
chr7:151471448
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(149): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
splice_region_variant&intron_variant | LOW | c.333-7C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 5/7 | chr7 | 151471448 | ||||||
chr7:151471618
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276-13T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471618 | ||||||
chr7:151471656
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.276-51A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471656 | ||||||
chr7:151471744
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(149): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.276-139G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471744 | ||||||
chr7:151471804
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.276-199C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471804 | ||||||
chr7:151471940
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.276-335G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471940 | ||||||
chr7:151472000
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0001g0255others(1): Show | 5 | HG01952.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-395T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472000 | ||||||
chr7:151472097
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0240a0001c0001t0001g0248 | 4 | HG02109.hp2 HG02280.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-492T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472097 | ||||||
chr7:151472183
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276-578G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472183 | ||||||
chr7:151472189
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.276-584G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472189 | ||||||
chr7:151472522
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-917G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472522 | ||||||
chr7:151472534
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0079 | 3 | NA18945.hp2 NA18956.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.276-929G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472534 | ||||||
chr7:151472658
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.276-1053G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472658 | ||||||
chr7:151472704
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(11): Show | 16 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.276-1099C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472704 | ||||||
chr7:151472730
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276-1125G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472730 | ||||||
chr7:151472774
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0002g0125 | 2 | HG00558.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.276-1169A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472774 | ||||||
chr7:151472933
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.276-1328G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472933 | ||||||
chr7:151473165
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0258others(2): Show | 7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.276-1560C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473165 | ||||||
chr7:151473184
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(11): Show | 16 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.276-1579C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473184 | ||||||
chr7:151473199
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.276-1594C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473199 | ||||||
chr7:151473385
|
C | T | 1 | a0001c0001t0003g0287 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.276-1780G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473385 | ||||||
chr7:151473581
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-1976G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473581 | ||||||
chr7:151473757
|
T | TA | 39 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(36): Show | 42 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.276-2153dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473757 | ||||||
chr7:151473829
|
T | C | 13 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(10): Show | 13 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.276-2224A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473829 | ||||||
chr7:151473865
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.276-2260A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473865 | ||||||
chr7:151473994
|
A | T | 28 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0035others(25): Show | 31 | HG00423.hp2 HG01167.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.276-2389T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473994 | ||||||
chr7:151474186
|
GT | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(156): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.276-2582delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474186 | ||||||
chr7:151474250
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.276-2645G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474250 | ||||||
chr7:151474266
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 24 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.276-2661G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474266 | ||||||
chr7:151474269
|
C | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0148 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.276-2664G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474269 | ||||||
chr7:151474330
|
G | A | 46 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0045others(43): Show | 51 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.276-2725C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474330 | ||||||
chr7:151474528
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0240others(5): Show | 11 | HG01243.hp1 HG01943.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.275+2805T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474528 | ||||||
chr7:151474574
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0227a0001c0001t0001g0258others(2): Show | 7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+2759T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474574 | ||||||
chr7:151474576
|
G | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(144): Show | 177 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.275+2757C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474576 | ||||||
chr7:151474672
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+2661A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474672 | ||||||
chr7:151474995
|
G | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(158): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.275+2338C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474995 | ||||||
chr7:151475124
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 25 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.275+2209A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475124 | ||||||
chr7:151475196
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.275+2137T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475196 | ||||||
chr7:151475389
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0122a0001c0001t0001g0139 | 4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1944A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475389 | ||||||
chr7:151475391
|
G | A | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0256others(17): Show | 24 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.275+1942C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475391 | ||||||
chr7:151475414
|
C | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 8 | HG02145.hp2 HG02717.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+1919G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475414 | ||||||
chr7:151475533
|
G | A | 1 | a0001c0001t0001g0011 | 3 | NA18981.hp2 NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.275+1800C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475533 | ||||||
chr7:151475625
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0012g0233 | 2 | HG00408.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.275+1708T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475625 | ||||||
chr7:151475705
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.275+1628G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475705 | ||||||
chr7:151475792
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0022others(24): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.275+1541A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475792 | ||||||
chr7:151475837
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.275+1496T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475837 | ||||||
chr7:151475859
|
A | T | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275+1474T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475859 | ||||||
chr7:151476082
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275+1251T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476082 | ||||||
chr7:151476129
|
G | A | 1 | a0001c0001t0001g0024 | 2 | NA18986.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.275+1204C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476129 | ||||||
chr7:151476152
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0280 | 3 | HG02630.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.275+1181A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476152 | ||||||
chr7:151476161
|
C | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0064a0001c0001t0002g0152 | 4 | HG02027.hp1 HG02074.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+1172G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476161 | ||||||
chr7:151476642
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275+691T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476642 | ||||||
chr7:151476740
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0143 | 3 | HG01256.hp2 HG01261.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.275+593G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476740 | ||||||
chr7:151476789
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.275+544T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476789 | ||||||
chr7:151476904
|
T | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(37): Show | 43 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.275+429A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476904 | ||||||
chr7:151476963
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.275+370A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476963 | ||||||
chr7:151477084
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275+249A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477084 | ||||||
chr7:151477130
|
C | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.275+203G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477130 | ||||||
chr7:151477200
|
C | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(115): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.275+133G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477200 | ||||||
chr7:151477222
|
G | A | 2 | a0001c0001t0005g0043a0001c0001t0005g0148 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.275+111C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477222 | ||||||
chr7:151477246
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.275+87G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477246 | ||||||
chr7:151477286
|
T | G | 1 | a0001c0001t0002g0091 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.275+47A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477286 | ||||||
chr7:151477452
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-37A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477452 | ||||||
chr7:151477516
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-101G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477516 | ||||||
chr7:151477553
|
A | G | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-138T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477553 | ||||||
chr7:151477591
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.193-176C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477591 | ||||||
chr7:151477947
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0122 | 3 | HG00735.hp2 HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.193-532C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477947 | ||||||
chr7:151478009
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.193-594A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478009 | ||||||
chr7:151478132
|
C | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-717G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478132 | ||||||
chr7:151478258
|
T | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG02109.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.193-843A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478258 | ||||||
chr7:151478342
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193-927A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478342 | ||||||
chr7:151478363
|
T | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(16): Show | 21 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-948A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478363 | ||||||
chr7:151478372
|
G | A | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(108): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.193-957C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478372 | ||||||
chr7:151478387
|
G | GA | 20 | a0001c0001t0001g0013a0001c0001t0001g0199a0001c0001t0001g0264others(17): Show | 22 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-973dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478387 | ||||||
chr7:151478431
|
C | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-1016G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478431 | ||||||
chr7:151478550
|
A | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0200 | 2 | HG00423.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.193-1135T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478550 | ||||||
chr7:151478649
|
T | C | 1 | a0001c0001t0002g0014 | 2 | NA18954.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.193-1234A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478649 | ||||||
chr7:151478871
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.193-1456C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478871 | ||||||
chr7:151478878
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.193-1463C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478878 | ||||||
chr7:151478937
|
AT | A | 15 | a0001c0001t0001g0013a0001c0001t0001g0215a0001c0001t0001g0264others(12): Show | 17 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-1523delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478937 | ||||||
chr7:151479006
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.193-1591G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479006 | ||||||
chr7:151479406
|
G | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0047 | 2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.193-1991C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479406 | ||||||
chr7:151479407
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.193-1992C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479407 | ||||||
chr7:151479409
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.193-1994T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479409 | ||||||
chr7:151479412
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.193-1997T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479412 | ||||||
chr7:151479465
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.193-2050T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479465 | ||||||
chr7:151479500
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048 | 3 | HG02280.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-2085C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479500 | ||||||
chr7:151479512
|
C | A | 6 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0284others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-2097G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479512 | ||||||
chr7:151479539
|
T | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0204 | 2 | HG03927.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.193-2124A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479539 | ||||||
chr7:151479543
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG00544.hp2 HG04115.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.193-2128G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479543 | ||||||
chr7:151479544
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193-2129C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479544 | ||||||
chr7:151479551
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193-2136G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479551 | ||||||
chr7:151479552
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048 | 3 | HG02280.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-2137C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479552 | ||||||
chr7:151479624
|
A | T | 4 | a0001c0001t0002g0062a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | HG01943.hp2 HG02293.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2209T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479624 | ||||||
chr7:151479640
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0257others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-2225C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479640 | ||||||
chr7:151479642
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.193-2227G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479642 | ||||||
chr7:151479645
|
A | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-2230T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479645 | ||||||
chr7:151479649
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.193-2234G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479649 | ||||||
chr7:151479662
|
G | A | 2 | a0001c0001t0005g0043a0001c0001t0005g0148 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.193-2247C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479662 | ||||||
chr7:151479664
|
T | C | 26 | a0001c0001t0001g0251a0001c0001t0002g0014a0001c0001t0002g0015others(23): Show | 28 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.193-2249A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479664 | ||||||
chr7:151479678
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-2263C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479678 | ||||||
chr7:151479682
|
C | CA | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 175 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.193-2268dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | ||||||
chr7:151479682
|
C | CAA | 13 | a0001c0001t0001g0013a0001c0001t0001g0180a0001c0001t0001g0181others(10): Show | 15 | HG01109.hp1 HG01433.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-2269_193-2268d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | ||||||
chr7:151479682
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2275_193-2268d others(10): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | ||||||
chr7:151479863
|
G | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-2448C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479863 | ||||||
chr7:151480031
|
C | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(178): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.193-2616G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480031 | ||||||
chr7:151480048
|
T | C | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.193-2633A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480048 | ||||||
chr7:151480061
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.193-2646C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480061 | ||||||
chr7:151480099
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.193-2684A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480099 | ||||||
chr7:151480309
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0257a0001c0001t0001g0264others(8): Show | 13 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-2894G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480309 | ||||||
chr7:151480412
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-2997G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480412 | ||||||
chr7:151480529
|
G | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3114C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480529 | ||||||
chr7:151480678
|
TATTA | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0258others(2): Show | 7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-3267_193-3264d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480678 | ||||||
chr7:151480685
|
TA | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(104): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.193-3271delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480685 | ||||||
chr7:151480686
|
A | T | 2 | a0001c0001t0001g0246a0001c0001t0006g0213 | 2 | HG01934.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.193-3271T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480686 | ||||||
chr7:151480689
|
A | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(122): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.193-3274T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480689 | ||||||
chr7:151480766
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.193-3351G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480766 | ||||||
chr7:151481066
|
C | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 43 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.193-3651G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481066 | ||||||
chr7:151481092
|
T | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.192+3645A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481092 | ||||||
chr7:151481130
|
CT | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0103others(12): Show | 19 | HG01243.hp1 HG01943.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+3606delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481130 | ||||||
chr7:151481337
|
T | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.192+3400A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481337 | ||||||
chr7:151481382
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.192+3355C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481382 | ||||||
chr7:151481455
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+3282G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481455 | ||||||
chr7:151481596
|
C | T | 8 | a0001c0001t0001g0057a0001c0001t0003g0055a0001c0001t0003g0282others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+3141G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481596 | ||||||
chr7:151481644
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+3093T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481644 | ||||||
chr7:151481766
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+2971G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481766 | ||||||
chr7:151481790
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.192+2947G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481790 | ||||||
chr7:151481814
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0047 | 2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.192+2923G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481814 | ||||||
chr7:151482321
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+2416A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482321 | ||||||
chr7:151482361
|
C | T | 37 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(34): Show | 40 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.192+2376G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482361 | ||||||
chr7:151482496
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192+2241A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482496 | ||||||
chr7:151482528
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.192+2209G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482528 | ||||||
chr7:151482572
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.192+2165T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482572 | ||||||
chr7:151482852
|
C | T | 39 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(36): Show | 42 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.192+1885G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482852 | ||||||
chr7:151482994
|
G | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1743C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482994 | ||||||
chr7:151483065
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1672G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483065 | ||||||
chr7:151483070
|
G | GC | 3 | a0001c0001t0001g0093a0001c0001t0002g0015a0001c0001t0002g0076 | 4 | HG00673.hp1 HG02040.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1666dupG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483070 | ||||||
chr7:151483277
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0122a0001c0001t0001g0139 | 4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1460C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483277 | ||||||
chr7:151483355
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192+1382G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483355 | ||||||
chr7:151483517
|
A | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(196): Show | 234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.192+1220T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483517 | ||||||
chr7:151483537
|
G | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.192+1200C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483537 | ||||||
chr7:151483549
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192+1188G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483549 | ||||||
chr7:151483890
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.192+847A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483890 | ||||||
chr7:151483965
|
A | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0142 | 2 | HG02135.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.192+772T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483965 | ||||||
chr7:151484046
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+691A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484046 | ||||||
chr7:151484306
|
T | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(37): Show | 43 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+431A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484306 | ||||||
chr7:151484536
|
A | G | 1 | a0001c0001t0003g0287 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.192+201T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484536 | ||||||
chr7:151484559
|
C | T | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.192+178G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484559 | ||||||
chr7:151484573
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.192+164T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484573 | ||||||
chr7:151484584
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0128 | 2 | NA18952.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.192+153C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484584 | ||||||
chr7:151484584
|
G | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+153C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484584 | ||||||
chr7:151484995
|
G | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.125-191C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151484995 | ||||||
chr7:151485375
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.125-571T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485375 | ||||||
chr7:151485571
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.125-767G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485571 | ||||||
chr7:151485759
|
G | A | 47 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(44): Show | 52 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.125-955C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485759 | ||||||
chr7:151485868
|
A | G | 1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.125-1064T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485868 | ||||||
chr7:151485931
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-1127A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485931 | ||||||
chr7:151486122
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.125-1318C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486122 | ||||||
chr7:151486679
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.125-1875G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486679 | ||||||
chr7:151486694
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0122 | 3 | HG00735.hp2 HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.125-1890C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486694 | ||||||
chr7:151487129
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.125-2325G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487129 | ||||||
chr7:151487439
|
A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.125-2635T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487439 | ||||||
chr7:151487464
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.125-2660G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487464 | ||||||
chr7:151487515
|
G | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.125-2711C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487515 | ||||||
chr7:151487525
|
GA | G | 29 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0033others(26): Show | 34 | HG00558.hp1 HG00738.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-2722delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487525 | ||||||
chr7:151487531
|
A | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0003g0055others(6): Show | 10 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-2727T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487531 | ||||||
chr7:151487534
|
A | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0031others(16): Show | 27 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.125-2730T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487534 | ||||||
chr7:151487640
|
G | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.125-2836C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487640 | ||||||
chr7:151487693
|
C | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0003g0055others(6): Show | 10 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-2889G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487693 | ||||||
chr7:151487834
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0196a0001c0001t0001g0237 | 4 | HG00099.hp1 HG01346.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3030T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487834 | ||||||
chr7:151487842
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.125-3038T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487842 | ||||||
chr7:151487877
|
T | C | 1 | a0001c0001t0002g0289 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124+3066A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487877 | ||||||
chr7:151487888
|
A | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+3055T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487888 | ||||||
chr7:151487899
|
C | T | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(175): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.124+3044G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487899 | ||||||
chr7:151488009
|
T | C | 35 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(32): Show | 38 | HG00423.hp2 HG00673.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+2934A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488009 | ||||||
chr7:151488118
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124+2825T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488118 | ||||||
chr7:151488169
|
G | A | 44 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(41): Show | 47 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.124+2774C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488169 | ||||||
chr7:151488281
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.124+2662G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488281 | ||||||
chr7:151488357
|
CTGAG | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0280a0001c0001t0001g0281 | 3 | HG01891.hp1 HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.124+2582_124+2585d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488357 | ||||||
chr7:151488443
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.124+2500A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488443 | ||||||
chr7:151488529
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.124+2414G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488529 | ||||||
chr7:151488570
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 297 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.124+2373C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488570 | ||||||
chr7:151488624
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+2319T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488624 | ||||||
chr7:151488698
|
A | C | 1 | a0001c0001t0002g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.124+2245T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488698 | ||||||
chr7:151488966
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124+1977G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488966 | ||||||
chr7:151488982
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+1961G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488982 | ||||||
chr7:151489011
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.124+1932C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489011 | ||||||
chr7:151489013
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.124+1930A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489013 | ||||||
chr7:151489085
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+1858G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489085 | ||||||
chr7:151489530
|
G | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(105): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.124+1413C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489530 | ||||||
chr7:151489552
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.124+1391A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489552 | ||||||
chr7:151489560
|
G | T | 1 | a0001c0001t0002g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.124+1383C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489560 | ||||||
chr7:151489611
|
T | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1332A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489611 | ||||||
chr7:151489632
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124+1311C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489632 | ||||||
chr7:151489677
|
T | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(113): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+1266A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489677 | ||||||
chr7:151489880
|
G | A | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1063C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489880 | ||||||
chr7:151489941
|
C | A | 22 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(19): Show | 24 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+1002G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489941 | ||||||
chr7:151490120
|
A | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+823T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490120 | ||||||
chr7:151490172
|
G | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+771C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490172 | ||||||
chr7:151490301
|
A | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(19): Show | 24 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+642T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490301 | ||||||
chr7:151490637
|
G | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.124+306C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490637 | ||||||
chr7:151490705
|
A | C | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124+238T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490705 | ||||||
chr7:151490749
|
A | G | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.124+194T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490749 | ||||||
chr7:151491077
|
C | A | 1 | a0001c0001t0001g0012 | 3 | HG01243.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.53-63G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491077 | ||||||
chr7:151491211
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.53-197A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491211 | ||||||
chr7:151491345
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-331A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491345 | ||||||
chr7:151491453
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-439G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491453 | ||||||
chr7:151491484
|
C | G | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-470G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491484 | ||||||
chr7:151491512
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-498C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491512 | ||||||
chr7:151491664
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53-650C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491664 | ||||||
chr7:151491736
|
CA | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(138): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.53-723delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491736 | ||||||
chr7:151491960
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-946G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491960 | ||||||
chr7:151492077
|
C | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0182others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1063G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492077 | ||||||
chr7:151492126
|
A | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-1112T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492126 | ||||||
chr7:151492378
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-1364C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492378 | ||||||
chr7:151492445
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.53-1431G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492445 | ||||||
chr7:151492509
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0011g0188 | 3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.53-1495G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492509 | ||||||
chr7:151492567
|
AG | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-1554delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492567 | ||||||
chr7:151492618
|
T | TA | 20 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0045others(17): Show | 21 | HG00735.hp1 HG01109.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.53-1605dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492618 | ||||||
chr7:151492640
|
G | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(120): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.53-1626C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492640 | ||||||
chr7:151492689
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.53-1675G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492689 | ||||||
chr7:151492696
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.53-1682G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492696 | ||||||
chr7:151492696
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 26 | HG00323.hp1 HG00438.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-1682G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492696 | ||||||
chr7:151492703
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53-1689G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492703 | ||||||
chr7:151492838
|
A | AT | 17 | a0001c0001t0001g0013a0001c0001t0001g0072a0001c0001t0001g0082others(14): Show | 19 | HG00280.hp2 HG00621.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.53-1825dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | ||||||
chr7:151492838
|
A | ATT | 8 | a0001c0001t0001g0034a0001c0001t0003g0055a0001c0001t0003g0282others(5): Show | 9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1826_53-1825dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | ||||||
chr7:151492838
|
A | ATTT | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(96): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.53-1827_53-1825dup others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | ||||||
chr7:151492838
|
A | ATTTT | 10 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0215others(7): Show | 10 | HG00544.hp1 HG00741.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1828_53-1825dup others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | ||||||
chr7:151492838
|
AT | A | 13 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-1825delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | ||||||
chr7:151492986
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1972G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492986 | ||||||
chr7:151492988
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.53-1974G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492988 | ||||||
chr7:151493025
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-2011A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493025 | ||||||
chr7:151493082
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.53-2068G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493082 | ||||||
chr7:151493088
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-2074C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493088 | ||||||
chr7:151493132
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0258others(2): Show | 7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-2118G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493132 | ||||||
chr7:151493144
|
A | C | 1 | a0001c0001t0001g0254 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.53-2130T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493144 | ||||||
chr7:151493659
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.53-2645T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493659 | ||||||
chr7:151493735
|
C | T | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-2721G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493735 | ||||||
chr7:151493846
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-2832T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493846 | ||||||
chr7:151493848
|
A | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0257a0001c0001t0001g0264others(6): Show | 11 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-2834T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493848 | ||||||
chr7:151493904
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.53-2890G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493904 | ||||||
chr7:151494025
|
T | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0257a0001c0001t0001g0264others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3011A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494025 | ||||||
chr7:151494122
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-3108T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494122 | ||||||
chr7:151494518
|
T | C | 6 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0051others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3504A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494518 | ||||||
chr7:151494625
|
G | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3611C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494625 | ||||||
chr7:151494654
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.53-3640C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494654 | ||||||
chr7:151494736
|
C | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-3722G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494736 | ||||||
chr7:151494736
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 8 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-3722G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494736 | ||||||
chr7:151494799
|
C | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-3785G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494799 | ||||||
chr7:151494961
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53-3947G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494961 | ||||||
chr7:151495007
|
G | A | 6 | a0001c0001t0002g0035a0001c0001t0002g0289a0001c0001t0002g0290others(3): Show | 7 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-3993C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495007 | ||||||
chr7:151495015
|
G | C | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-4001C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495015 | ||||||
chr7:151495234
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.53-4220G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495234 | ||||||
chr7:151495301
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.53-4287A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495301 | ||||||
chr7:151495401
|
C | T | 1 | a0001c0001t0001g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.53-4387G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495401 | ||||||
chr7:151495576
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(132): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.53-4562G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495576 | ||||||
chr7:151495591
|
T | C | 1 | a0001c0001t0010g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53-4577A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495591 | ||||||
chr7:151495674
|
G | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-4660C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495674 | ||||||
chr7:151495722
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.53-4708G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495722 | ||||||
chr7:151496029
|
C | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0189 | 4 | HG02027.hp2 NA18944.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5015G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496029 | ||||||
chr7:151496080
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0011g0188 | 3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.53-5066G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496080 | ||||||
chr7:151496116
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.53-5102G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496116 | ||||||
chr7:151496126
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-5112G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496126 | ||||||
chr7:151496282
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-5268G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496282 | ||||||
chr7:151496562
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-5548C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496562 | ||||||
chr7:151496588
|
A | G | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-5574T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496588 | ||||||
chr7:151496658
|
G | A | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-5644C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496658 | ||||||
chr7:151496945
|
A | AT | 16 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0109others(13): Show | 16 | HG00280.hp1 HG00544.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5932dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496945 | ||||||
chr7:151496945
|
AT | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(34): Show | 39 | HG00438.hp2 HG00735.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.53-5932delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496945 | ||||||
chr7:151497011
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-5997C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497011 | ||||||
chr7:151497020
|
T | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(148): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.53-6006A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497020 | ||||||
chr7:151497214
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0184 | 2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.53-6200A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497214 | ||||||
chr7:151497318
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-6304A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497318 | ||||||
chr7:151497362
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-6348G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497362 | ||||||
chr7:151497387
|
C | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-6373G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497387 | ||||||
chr7:151497724
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-6710G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497724 | ||||||
chr7:151497842
|
C | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.53-6828G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497842 | ||||||
chr7:151497943
|
C | A | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-6929G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497943 | ||||||
chr7:151497968
|
C | G | 1 | a0001c0001t0001g0288 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.53-6954G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497968 | ||||||
chr7:151498137
|
A | C | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7123T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498137 | ||||||
chr7:151498227
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-7213T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498227 | ||||||
chr7:151498242
|
G | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-7228C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498242 | ||||||
chr7:151498448
|
C | A | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7434G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498448 | ||||||
chr7:151498456
|
A | C | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7442T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498456 | ||||||
chr7:151498615
|
C | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-7601G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498615 | ||||||
chr7:151498804
|
T | TAAG | 24 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(21): Show | 26 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-7793_53-7791dup others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498804 | ||||||
chr7:151498901
|
TC | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-7888delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498901 | ||||||
chr7:151499142
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0275 | 2 | NA18949.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.53-8128C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499142 | ||||||
chr7:151499249
|
TG | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-8236delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499249 | ||||||
chr7:151499329
|
GC | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0292 | 3 | HG02055.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-8316delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499329 | ||||||
chr7:151499373
|
G | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-8359C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499373 | ||||||
chr7:151499707
|
T | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(21): Show | 26 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-8693A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499707 | ||||||
chr7:151499742
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0187a0001c0001t0001g0229others(3): Show | 8 | NA18965.hp1 NA18974.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-8728G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499742 | ||||||
chr7:151499861
|
T | C | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-8847A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499861 | ||||||
chr7:151499884
|
C | G | 1 | a0001c0001t0002g0061 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.53-8870G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499884 | ||||||
chr7:151500017
|
G | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-9003C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500017 | ||||||
chr7:151500039
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-9025G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500039 | ||||||
chr7:151500116
|
A | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-9102T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500116 | ||||||
chr7:151500154
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.53-9140T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500154 | ||||||
chr7:151500194
|
A | T | 1 | a0001c0001t0003g0283 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53-9180T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500194 | ||||||
chr7:151500367
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-9353T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500367 | ||||||
chr7:151500400
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0122a0001c0001t0001g0139 | 4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-9386C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500400 | ||||||
chr7:151500420
|
C | CA | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01943.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.53-9407dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500420 | ||||||
chr7:151500455
|
A | C | 1 | a0001c0001t0004g0005 | 3 | NA18981.hp1 NA19005.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.53-9441T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500455 | ||||||
chr7:151500585
|
G | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-9571C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500585 | ||||||
chr7:151500600
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(17): Show | 24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-9586G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500600 | ||||||
chr7:151500606
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0257a0001c0001t0001g0264others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-9592T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500606 | ||||||
chr7:151500649
|
G | C | 9 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0224others(6): Show | 11 | HG00673.hp2 HG02083.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-9635C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500649 | ||||||
chr7:151500690
|
T | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0047 | 2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.53-9676A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500690 | ||||||
chr7:151500727
|
T | G | 1 | a0001c0001t0001g0274 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53-9713A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500727 | ||||||
chr7:151500801
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.53-9787A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500801 | ||||||
chr7:151500974
|
AC | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-9961delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500974 | ||||||
chr7:151501002
|
A | G | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-9988T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501002 | ||||||
chr7:151501037
|
A | C | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-10023T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501037 | ||||||
chr7:151501562
|
T | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0257a0001c0001t0001g0264others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-10548A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501562 | ||||||
chr7:151501621
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53-10607A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501621 | ||||||
chr7:151501725
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53-10711C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501725 | ||||||
chr7:151501742
|
C | T | 1 | a0001c0001t0009g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53-10728G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501742 | ||||||
chr7:151501774
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.53-10760A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501774 | ||||||
chr7:151501833
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG01099.hp1 HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.53-10819G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501833 | ||||||
chr7:151501834
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53-10820C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501834 | ||||||
chr7:151501964
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-10950C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501964 | ||||||
chr7:151502006
|
C | T | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-10992G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502006 | ||||||
chr7:151502094
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53-11080C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502094 | ||||||
chr7:151502162
|
G | A | 1 | a0001c0001t0009g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53-11148C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502162 | ||||||
chr7:151502187
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.53-11173C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502187 | ||||||
chr7:151502228
|
C | CA | 11 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(8): Show | 11 | HG00438.hp2 HG01192.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-11215dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502228 | ||||||
chr7:151502228
|
CA | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(115): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.53-11215delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502228 | ||||||
chr7:151502294
|
G | C | 1 | a0001c0001t0002g0289 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-11280C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502294 | ||||||
chr7:151502411
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0142 | 2 | HG02135.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.53-11397T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502411 | ||||||
chr7:151502421
|
CA | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-11408delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502421 | ||||||
chr7:151502430
|
AAACTTTA others(48): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-11471_53-11417d others(57): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502430 | ||||||
chr7:151502524
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-11510A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502524 | ||||||
chr7:151502570
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0260 | 2 | HG01943.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.53-11556T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502570 | ||||||
chr7:151502712
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53-11698G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502712 | ||||||
chr7:151502727
|
G | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-11713C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502727 | ||||||
chr7:151502812
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-11798T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502812 | ||||||
chr7:151502931
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.53-11917C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502931 | ||||||
chr7:151503051
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-12037G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503051 | ||||||
chr7:151503053
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.53-12039T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503053 | ||||||
chr7:151503251
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-12237C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503251 | ||||||
chr7:151503481
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.53-12467G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503481 | ||||||
chr7:151503656
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-12642C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503656 | ||||||
chr7:151503721
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-12707A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503721 | ||||||
chr7:151503763
|
G | GA | 16 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0103others(13): Show | 18 | HG01943.hp1 HG01975.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.53-12750dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503763 | ||||||
chr7:151503763
|
GA | G | 32 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(29): Show | 45 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.53-12750delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503763 | ||||||
chr7:151503776
|
A | AAT | 8 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0045others(5): Show | 10 | HG01099.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-12763_53-12762i others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | ||||||
chr7:151503776
|
A | AT | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(113): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.53-12763dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | ||||||
chr7:151503776
|
A | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0161a0001c0001t0002g0044others(6): Show | 10 | HG00735.hp1 HG01109.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-12762T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | ||||||
chr7:151503802
|
G | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0234a0001c0001t0006g0213others(1): Show | 4 | NA18955.hp2 NA18974.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-12788C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503802 | ||||||
chr7:151503822
|
G | C | 1 | a0001c0001t0001g0216 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.53-12808C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503822 | ||||||
chr7:151503852
|
T | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-12838A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503852 | ||||||
chr7:151503913
|
T | C | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-12899A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503913 | ||||||
chr7:151503945
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-12931T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503945 | ||||||
chr7:151504018
|
TAGG | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-13007_53-13005d others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504018 | ||||||
chr7:151504071
|
G | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.53-13057C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504071 | ||||||
chr7:151504213
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.53-13199A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504213 | ||||||
chr7:151504234
|
C | A | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-13220G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504234 | ||||||
chr7:151504473
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-13459C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504473 | ||||||
chr7:151504562
|
C | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-13548G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504562 | ||||||
chr7:151504637
|
A | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-13623T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504637 | ||||||
chr7:151504671
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-13657G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504671 | ||||||
chr7:151504672
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-13658C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504672 | ||||||
chr7:151504723
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-13709G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504723 | ||||||
chr7:151504867
|
C | CA | 7 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02280.hp1 HG02602.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-13854dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504867 | ||||||
chr7:151505043
|
G | GA | 12 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0094others(9): Show | 18 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-14030dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505043 | ||||||
chr7:151505043
|
G | GAA | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0222others(8): Show | 13 | HG00673.hp2 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-14031_53-14030d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505043 | ||||||
chr7:151505054
|
C | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.53-14040G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505054 | ||||||
chr7:151505102
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.53-14088G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505102 | ||||||
chr7:151505102
|
C | CA | 27 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0045others(24): Show | 29 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.53-14089dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505102 | ||||||
chr7:151505169
|
C | CA | 8 | a0001c0001t0001g0006a0001c0001t0001g0085a0001c0001t0001g0086others(5): Show | 10 | HG00597.hp2 HG02293.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-14156dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505169 | ||||||
chr7:151505169
|
CA | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(144): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.53-14156delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505169 | ||||||
chr7:151505210
|
T | G | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-14196A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505210 | ||||||
chr7:151505250
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52+14210T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505250 | ||||||
chr7:151505550
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.52+13910C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505550 | ||||||
chr7:151505907
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.52+13553G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505907 | ||||||
chr7:151505935
|
AAACT | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+13521_52+13524d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505935 | ||||||
chr7:151505952
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0128 | 2 | NA18952.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.52+13508A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505952 | ||||||
chr7:151505965
|
A | G | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+13495T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505965 | ||||||
chr7:151505972
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.52+13488G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505972 | ||||||
chr7:151506013
|
T | C | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.52+13447A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506013 | ||||||
chr7:151506153
|
G | GA | 5 | a0001c0001t0001g0008a0001c0001t0001g0092a0001c0001t0001g0126others(2): Show | 7 | HG00558.hp2 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+13306dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506153 | ||||||
chr7:151506188
|
C | CT | 10 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0108others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+13271dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506188 | ||||||
chr7:151506238
|
G | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(1): Show | 4 | HG02280.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+13222C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506238 | ||||||
chr7:151506328
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+13132C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506328 | ||||||
chr7:151506455
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+13005C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506455 | ||||||
chr7:151506510
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.52+12950A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506510 | ||||||
chr7:151506570
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.52+12890A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506570 | ||||||
chr7:151506936
|
G | C | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+12524C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506936 | ||||||
chr7:151507156
|
C | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+12304G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507156 | ||||||
chr7:151507258
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0160 | 2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.52+12202T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507258 | ||||||
chr7:151507275
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+12185G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507275 | ||||||
chr7:151507400
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(129): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.52+12060G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507400 | ||||||
chr7:151507407
|
A | AT | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(129): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.52+12052dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507407 | ||||||
chr7:151507407
|
A | ATAT | 17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0255others(14): Show | 21 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+12052_52+12053i others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507407 | ||||||
chr7:151507453
|
T | C | 1 | a0001c0001t0010g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.52+12007A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507453 | ||||||
chr7:151507471
|
CAT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0074others(1): Show | 5 | HG00408.hp1 NA18941.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+11987_52+11988d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507471 | ||||||
chr7:151507473
|
T | G | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+11987A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507473 | ||||||
chr7:151507477
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+11983G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507477 | ||||||
chr7:151507598
|
T | G | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.52+11862A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507598 | ||||||
chr7:151507618
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52+11842C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507618 | ||||||
chr7:151507679
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.52+11781T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507679 | ||||||
chr7:151507760
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+11700A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507760 | ||||||
chr7:151507930
|
T | C | 1 | a0001c0001t0013g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.52+11530A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507930 | ||||||
chr7:151508110
|
T | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0096 | 3 | HG01167.hp2 HG01358.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.52+11350A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508110 | ||||||
chr7:151508125
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+11335A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508125 | ||||||
chr7:151508243
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52+11217A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508243 | ||||||
chr7:151508420
|
T | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0247 | 3 | HG00673.hp2 HG02083.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.52+11040A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508420 | ||||||
chr7:151508588
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+10872T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508588 | ||||||
chr7:151508634
|
G | GT | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(119): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.52+10825dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508634 | ||||||
chr7:151508634
|
G | GTT | 8 | a0001c0001t0001g0034a0001c0001t0003g0055a0001c0001t0003g0282others(5): Show | 9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+10824_52+10825d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508634 | ||||||
chr7:151508698
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.52+10762G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508698 | ||||||
chr7:151508802
|
T | C | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.52+10658A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508802 | ||||||
chr7:151508810
|
G | C | 1 | a0001c0001t0001g0278 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.52+10650C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508810 | ||||||
chr7:151509089
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+10371C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509089 | ||||||
chr7:151509125
|
C | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+10335G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509125 | ||||||
chr7:151509140
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+10320T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509140 | ||||||
chr7:151509142
|
G | A | 6 | a0001c0001t0002g0035a0001c0001t0002g0289a0001c0001t0002g0290others(3): Show | 7 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+10318C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509142 | ||||||
chr7:151509161
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.52+10299G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509161 | ||||||
chr7:151509236
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.52+10224C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509236 | ||||||
chr7:151509270
|
C | A | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+10190G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509270 | ||||||
chr7:151509553
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(144): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.52+9907G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509553 | ||||||
chr7:151509578
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.52+9882G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509578 | ||||||
chr7:151509604
|
C | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+9856G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509604 | ||||||
chr7:151509685
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.52+9775A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509685 | ||||||
chr7:151509753
|
T | C | 1 | a0001c0001t0003g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+9707A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509753 | ||||||
chr7:151509807
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+9653A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509807 | ||||||
chr7:151509839
|
G | A | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+9621C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509839 | ||||||
chr7:151509858
|
G | A | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+9602C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509858 | ||||||
chr7:151510049
|
GAA | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+9409_52+9410del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510049 | ||||||
chr7:151510098
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+9362G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510098 | ||||||
chr7:151510101
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.52+9359A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510101 | ||||||
chr7:151510391
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+9069A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510391 | ||||||
chr7:151510530
|
A | C | 1 | a0001c0001t0002g0073 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.52+8930T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510530 | ||||||
chr7:151510847
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+8613C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510847 | ||||||
chr7:151510887
|
G | A | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+8573C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510887 | ||||||
chr7:151510985
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.52+8475C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510985 | ||||||
chr7:151511091
|
T | TA | 8 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(5): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+8368dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511091 | ||||||
chr7:151511244
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.52+8216C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511244 | ||||||
chr7:151511347
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(27): Show | 43 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.52+8113A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511347 | ||||||
chr7:151511379
|
G | T | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+8081C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511379 | ||||||
chr7:151511449
|
C | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+8011G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511449 | ||||||
chr7:151511572
|
CT | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0234a0001c0001t0001g0255others(5): Show | 10 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+7887delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511572 | ||||||
chr7:151511664
|
C | CT | 13 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0106others(10): Show | 16 | HG00735.hp1 HG01515.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.52+7795dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511664 | ||||||
chr7:151511664
|
C | CTT | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+7794_52+7795dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511664 | ||||||
chr7:151511710
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0184 | 3 | HG02040.hp2 HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.52+7750G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511710 | ||||||
chr7:151511735
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.52+7725G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511735 | ||||||
chr7:151511740
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0022others(24): Show | 35 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.52+7720C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511740 | ||||||
chr7:151511902
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.52+7558A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511902 | ||||||
chr7:151511926
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.52+7534A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511926 | ||||||
chr7:151511981
|
A | C | 1 | a0001c0004t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52+7479T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511981 | ||||||
chr7:151512038
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.52+7422C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512038 | ||||||
chr7:151512108
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0091 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.52+7352C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512108 | ||||||
chr7:151512305
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.52+7155C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512305 | ||||||
chr7:151512306
|
T | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(1): Show | 4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+7154A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512306 | ||||||
chr7:151512688
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.52+6772G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512688 | ||||||
chr7:151512698
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+6762T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512698 | ||||||
chr7:151512771
|
A | G | 1 | a0001c0001t0001g0018 | 2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+6689T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512771 | ||||||
chr7:151512891
|
G | A | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+6569C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512891 | ||||||
chr7:151512894
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.52+6566G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512894 | ||||||
chr7:151513053
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0045others(20): Show | 25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+6407C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513053 | ||||||
chr7:151513091
|
A | G | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+6369T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513091 | ||||||
chr7:151513124
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+6336G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513124 | ||||||
chr7:151513272
|
T | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+6188A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513272 | ||||||
chr7:151513525
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(114): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.52+5935C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513525 | ||||||
chr7:151513674
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.52+5786A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513674 | ||||||
chr7:151513739
|
T | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+5721A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513739 | ||||||
chr7:151513754
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52+5706C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513754 | ||||||
chr7:151513819
|
T | A | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+5641A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513819 | ||||||
chr7:151513841
|
T | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02135.hp2 NA18945.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5619A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513841 | ||||||
chr7:151513875
|
T | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0143 | 3 | HG01256.hp2 HG01261.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.52+5585A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513875 | ||||||
chr7:151513975
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.52+5485C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513975 | ||||||
chr7:151514019
|
G | C | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5441C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514019 | ||||||
chr7:151514184
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+5276T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514184 | ||||||
chr7:151514415
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01943.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52+5045C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514415 | ||||||
chr7:151514520
|
T | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+4940A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514520 | ||||||
chr7:151514522
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+4938C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514522 | ||||||
chr7:151514699
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(114): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.52+4761G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514699 | ||||||
chr7:151515068
|
C | CAA | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(113): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.52+4390_52+4391dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | ||||||
chr7:151515068
|
C | CAAAA | 9 | a0001c0001t0001g0012a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 11 | HG01243.hp1 HG01943.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+4388_52+4391dup others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | ||||||
chr7:151515068
|
C | CAAAAA | 15 | a0001c0001t0001g0013a0001c0001t0001g0042a0001c0001t0001g0264others(12): Show | 17 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+4387_52+4391dup others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | ||||||
chr7:151515068
|
C | CAAAAAA | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+4386_52+4391dup others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | ||||||
chr7:151515068
|
CA | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.52+4391delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | ||||||
chr7:151515138
|
A | G | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+4322T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515138 | ||||||
chr7:151515175
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0182others(1): Show | 6 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+4285T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515175 | ||||||
chr7:151515220
|
A | G | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+4240T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515220 | ||||||
chr7:151515686
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.52+3774A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515686 | ||||||
chr7:151515853
|
A | C | 1 | a0001c0001t0003g0282 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52+3607T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515853 | ||||||
chr7:151515943
|
T | C | 15 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+3517A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515943 | ||||||
chr7:151515980
|
T | G | 1 | a0001c0001t0001g0131 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.52+3480A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515980 | ||||||
chr7:151516043
|
T | TTTAAC | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(124): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.52+3416_52+3417ins others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516043 | ||||||
chr7:151516126
|
T | C | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+3334A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516126 | ||||||
chr7:151516157
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.52+3303C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516157 | ||||||
chr7:151516390
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+3070G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516390 | ||||||
chr7:151516391
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+3069C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516391 | ||||||
chr7:151516407
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0240a0001c0001t0001g0248others(1): Show | 5 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+3053C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516407 | ||||||
chr7:151516617
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52+2843A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516617 | ||||||
chr7:151516622
|
C | CA | 38 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 52 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.52+2837dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | ||||||
chr7:151516622
|
C | CAA | 8 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG00597.hp1 HG02135.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+2836_52+2837dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | ||||||
chr7:151516622
|
CA | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(71): Show | 82 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.52+2837delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | ||||||
chr7:151516622
|
CAA | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(114): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.52+2836_52+2837del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | ||||||
chr7:151516881
|
G | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(146): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.52+2579C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516881 | ||||||
chr7:151517352
|
G | C | 1 | a0001c0001t0005g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+2108C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517352 | ||||||
chr7:151517361
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+2099A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517361 | ||||||
chr7:151517368
|
CG | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(98): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.52+2091delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517368 | ||||||
chr7:151517369
|
GGA | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01433.hp1 HG01496.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2089_52+2090del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517369 | ||||||
chr7:151517370
|
G | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0250others(19): Show | 25 | HG00544.hp1 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+2090C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | ||||||
chr7:151517370
|
G | GA | 16 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 16 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.52+2089dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | ||||||
chr7:151517370
|
G | GAA | 6 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0001t0002g0051others(3): Show | 6 | HG00735.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+2088_52+2089dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | ||||||
chr7:151517370
|
GA | G | 17 | a0001c0001t0001g0072a0001c0001t0001g0153a0001c0001t0001g0167others(14): Show | 18 | HG01943.hp2 HG01975.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+2089delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | ||||||
chr7:151517371
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.52+2089T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517371 | ||||||
chr7:151517496
|
T | A | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(1): Show | 4 | NA18963.hp2 NA18988.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+1964A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517496 | ||||||
chr7:151517620
|
C | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(123): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.52+1840G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517620 | ||||||
chr7:151517690
|
C | CA | 17 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 18 | HG00438.hp1 HG00735.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+1769dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517690 | ||||||
chr7:151517690
|
CA | C | 9 | a0001c0001t0001g0166a0001c0001t0002g0058a0001c0001t0003g0055others(6): Show | 9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1769delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517690 | ||||||
chr7:151517710
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+1750A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517710 | ||||||
chr7:151517711
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.52+1749C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517711 | ||||||
chr7:151517777
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.52+1683A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517777 | ||||||
chr7:151517783
|
T | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 26 | HG00323.hp1 HG00438.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+1677A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517783 | ||||||
chr7:151517837
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.52+1623A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517837 | ||||||
chr7:151518009
|
A | AAGCCCAG others(15): Show |
1 | a0001c0001t0001g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.52+1450_52+1451ins others(22): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518009 | ||||||
chr7:151518012
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.52+1448C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518012 | ||||||
chr7:151518047
|
T | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+1413A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518047 | ||||||
chr7:151518095
|
C | T | 7 | a0001c0001t0003g0055a0001c0001t0003g0282a0001c0001t0003g0283others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1365G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518095 | ||||||
chr7:151518230
|
G | C | 1 | a0001c0001t0002g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.52+1230C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518230 | ||||||
chr7:151518235
|
G | A | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+1225C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518235 | ||||||
chr7:151518368
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0288a0001c0001t0002g0035others(12): Show | 17 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.52+1092A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518368 | ||||||
chr7:151518399
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+1061G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518399 | ||||||
chr7:151518498
|
T | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.52+962A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518498 | ||||||
chr7:151518525
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.52+935T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518525 | ||||||
chr7:151518696
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52+764C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518696 | ||||||
chr7:151518864
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.52+596T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518864 | ||||||
chr7:151518929
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(26): Show | 42 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.52+531G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518929 | ||||||
chr7:151519267
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.52+193C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519267 | ||||||
chr7:151519279
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52+181C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519279 | ||||||
chr7:151519401
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.52+59G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519401 |